Improved nanobodies tm for the treatment of aggregation-mediated disorders

0001The present invention relates to improved Nanobodies™ against von Willebrand Factor (vWF), as well as to polypeptides comprising or essentially consisting of one or more of such Nanobodies. <i>[Note: Nanobody</i>™, <i>Nanobodies</i>™ <i>and Nanoclone</i>™ <i>are trademarks of Ablynx N.V.]</i>

0002The invention also relates to nucleic acids encoding such Nanobodies and polypeptides; to methods for preparing such Nanobodies and polypeptides; to host cells expressing or capable of expressing such Nanobodies or polypeptides; to compositions comprising such Nanobodies, polypeptides, nucleic acids or host cells; and to uses of such Nanobodies, such polypeptides, such nucleic acids, such host cells or such compositions, in particular for prophylactic, therapeutic or diagnostic purposes, such as the prophylactic, therapeutic or diagnostic purposes mentioned below.

0003Other aspects, embodiments, advantages and applications of the invention will become clear from the further description hereinbelow.

0004<patcit id="pcit0001" dnum="WO04062551A"><text>WO 04/062551</text></patcit> of Applicant relates to Nanobodies against Von Willebrand Factor (vWF) and to the preparation and use thereof, in particular for the prevention and/or treatment of diseases and disorders relating to platelet-mediated aggregation.

0005The anti-vWF Nanobodies according to <patcit id="pcit0002" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may be humanized and may be monovalent or multivalent, the latter of which leads to increased affinity for vWF. The anti-vWF Nanobodies according to <patcit id="pcit0003" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may also be multispecific, and may in particular be in the form of a multispecific construct comprising two or more Nanobodies against vWF and a further Nanobody directed against a serum protein such as human serum albumin, which leads to an increased half-life in vivo.

0006The anti-vWF Nanobodies described in <patcit id="pcit0004" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may be directed against any epitope or conformation of vWF (such as the A1 domain or A3 domain), but are preferably directed against the A1 domain, and in particular against the activated conformation of the A1 domain.

0007<patcit id="pcit0005" dnum="WO04062551A"><text>WO 04/062551</text></patcit> also describes the preparation of the anti-vWF Nanobodies, nucleotide sequences encoding the anti-vWF Nanobodies, as well as pharmaceutical compositions comprising the anti-vWF Nanobodies.

0008The anti-vWF Nanobodies and compositions described in <patcit id="pcit0006" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may be used for the prevention and treatment of diseases and disorders related to platelet-mediated aggregation, such as the formation of a non-occlusive thrombus, the formation of an occlusive thrombus, arterial thrombus formation, acute coronary occlusion, peripheral arterial occlusive disease, restenosis and disorders arising from coronary by-pass graft, coronary artery valve replacement and coronary interventions such angioplasty, stenting or atherectomy, hyperplasia after angioplasty, atherectomy or arterial stenting, occlusive syndrome in a vascular system or lack of patency of diseased arteries, thrombotic thrombocytopenic purpura (TTP), transient cerebral ischemic attack, unstable or stable angina pectoris, cerebral infarction, HELLP syndrome, carotid endarterectomy, carotid artery stenosis, critical limb ischaemia, cardioembolism, peripheral vascular disease, restenosis and myocardial infarction..

0009The pharmaceutical compositions described in <patcit id="pcit0007" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may be suitable for intravenous, subcutaneous, oral, sublingual, topical, nasal, vaginal or rectal administration, or for administration by inhalation; and may also comprise a trombolytic agent, such as staphylokinase, tissue plasminogen activator, streptokinase, single chain streptokinase, urokinase and acyl plasminogen streptokinase complex. The anti-vWF Nanobodies described in <patcit id="pcit0008" dnum="WO04062551A"><text>WO 04/062551</text></patcit> may also be used for diagnostic purposes (optionally in the form of a kit-of-parts) or in coatings for medical devices such as stents

0010It is a general object of the present invention to provide Nanobodies against vWF, in particular against human vWF.

0011In particular, it is an object of the present invention to provide Nanobodies against vWF, in particular against human vWF, and to provide proteins or polypeptides comprising the same, that are suitable for therapeutic and/or diagnostic use, and in particular for the prevention, treatment and/or diagnosis of one or more diseases and disorders associated with and/or mediated by vWF such as those mentioned above, and/or that can be used in the preparation of a pharmaceutical composition for the prevention and/or treatment of one or more diseases associated with and/or mediated by vWF, such as those mentioned above.

0012More in particular, it is an object of the invention to provide Nanobodies against vWF, and to provide proteins and polypeptides comprising the same, that are either an alternative to the Nanobodies and polypeptides against vWF described in <patcit id="pcit0009" dnum="WO04062551A"><text>WO 04/062551</text></patcit> and/or that have one or more improved properties or characteristics, compared to the Nanobodies and polypeptides against vWF described in <patcit id="pcit0010" dnum="WO04062551A"><text>WO 04/062551</text></patcit>.

0013More in particular, it is an object of the invention to provide Nanobodies against vWF, and to provide proteins or polypeptides comprising the same, that are improved compared to the Nanobodies and polypeptides against vWF described in <patcit id="pcit0011" dnum="WO04062551A"><text>WO 04/062551</text></patcit> with respect to one or more of the following properties or characteristics: <ul id="ul0001" list-style="dash" compact="compact"><li>increased affinity for vWF, either in a monovalent format, in a multivalent format (for example in a bivalent format) and/or in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0012" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow);</li><li>better suitability for formatting in a multivalent format (for example in a bivalent format);</li><li>better suitability for formatting in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0013" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow);</li><li>improved suitability or susceptibility for "humanizing" substitutions (as defined herein); and/or</li><li>less immunogenicity, either in a monovalent format, in a multivalent format (for example in a bivalent format) and/or in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0014" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow) in a monovalent format;</li><li>increased stability, either in a monovalent format, in a multivalent format (for example in a bivalent format) and/or in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0015" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow) in a monovalent format;</li><li>increased specificity towards vWF, either in a monovalent format, in a multivalent format (for example in a bivalent format) and/or in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0016" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow) in a monovalent format;</li><li>decreased or where desired increased cross-reactivity with vWF from different species; and/or</li><li>one or more other improved properties desirable for pharmaceutical use (including prophylactic use and/or therapeutic use) and/or for diagnostic use (including but not limited to use for imaging purposes), either in a monovalent format, in a multivalent format (for example in a bivalent format) and/or in a multispecific format (for example one of the multispecific formats described in <patcit id="pcit0017" dnum="WO04062551A"><text>WO 04/062551</text></patcit> or hereinbelow).</li></ul>

0014These objects are achieved by the Nanobodies against vWF and by the polypeptides described herein. The Nanobodies against vWF and polypeptides described herein are in particular directed against human vWF, but it is included within the scope of the invention that some of the anti-vWF Nanobodies and polypeptides of the invention may show cross-reactivity with vWF from other vertebrate animals, in particular from other warm-blooded animals, more in particular from other mammals, and in particular from other species of primates, such as the baboons used in the Examples below. However, as with anti-vWF Nanobodies described in <patcit id="pcit0018" dnum="WO04062551A"><text>WO 04/062551</text></patcit>, the present invention in its broadest sense is not particularly limited to or defined by a specific epitope, domain or confirmation of vWF against which the Nanobodies and polypeptides of the invention are directed. However, it is generally assumed and preferred that the Nanobodies and polypeptides of the invention are directed against the A1 domain of vWF, either in its activated or non-activated confirmation.

0015Thus, in a first aspect, the invention relates to a Nanobody (as defined herein), against vWF, which consist of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: i) CDR1 comprises or essentially consists of an amino acid sequence chosen from the group consisting of: <tables id="tabl0001" num="0001"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>NYGMG</entry><entry>[SEQ ID NO: 15]</entry></row><row><entry>SYTLG</entry><entry>[SEQ ID NO: 16]</entry></row><row><entry>NYNMG</entry><entry>[SEQ ID NO: 17]</entry></row><row><entry>SSAMA</entry><entry>[SEQ ID NO: 18]</entry></row><row><entry>YYNTG</entry><entry>[SEQ ID NO: 19]</entry></row><row><entry>IGAMG</entry><entry>[SEQ ID NO: 20]</entry></row><row><entry>IGTMG</entry><entry>[SEQ ID NO: 21]</entry></row><row><entry>YNPMG</entry><entry>[SEQ ID NO: 22]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0001"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0002"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: ii) CDR2 comprises or essentially consist of an amino acid sequence chosen from the group consisting of: <tables id="tabl0002" num="0002"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="44mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SISWSGTYTAYSDNVKG</entry><entry>[SEQ ID NO: 23]</entry></row><row><entry>GISWSGVSTDYAEFAKG</entry><entry>[SEQ ID NO: 24]</entry></row><row><entry>TSISWSGSYTAYADNVKG</entry><entry>[SEQ ID NO: 25]</entry></row><row><entry>SISWSGMSTYYTDSVKG</entry><entry>[SEQ ID NO: 26]</entry></row><row><entry>TITSGGRTSYADSVKG</entry><entry>[SEQ ID NO: 27]</entry></row><row><entry>AISWSGGLTYYADSVKG</entry><entry>[SEQ ID NO: 28]</entry></row><row><entry>TITSGGSTNYADPVKG</entry><entry>[SEQ ID NO: 29]</entry></row><row><entry>TITSGGSTNYADSVKG</entry><entry>[SEQ ID NO: 30]</entry></row><row><entry>AISRTGGSTYYARSVEG</entry><entry>[SEQ ID NO: 31]</entry></row><row><entry>AISRTGGSTYYPDSVEG</entry><entry>[SEQ ID NO: 32]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0003" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0004" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: iii) CDR3 comprises or essentially consists of an amino acid sequence chosen from the group consisting of: <tables id="tabl0003" num="0003"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>QSRYRSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 33]</entry></row><row><entry>LGRYRSNWRNIGQYDY</entry><entry>[SEQ ID NO: 34]</entry></row><row><entry>QSRYSSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 35]</entry></row><row><entry>SNRYRTHTTQAMYNY</entry><entry>[SEQ ID NO: 36]</entry></row><row><entry>WDGKRAP</entry><entry>[SEQ ID NO: 37]</entry></row><row><entry>NRRQKTVQMGERAYDY</entry><entry>[SEQ ID NO: 38]</entry></row><row><entry>NLKQGSYGYRFNDY</entry><entry>[SEQ ID NO: 39]</entry></row><row><entry>NLKQGDYGYRFNDY</entry><entry>[SEQ ID NO: 40]</entry></row><row><entry>AGVRAEDGRVRTLPSEYNF</entry><entry>[SEQ ID NO: 41]</entry></row><row><entry>AGVRAEDGRVRTLPSEYTF</entry><entry>[SEQ ID NO: 42]</entry></row><row><entry>AGVRAEDGRVRSLPSEYTF</entry><entry>[SEQ ID NO: 43]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0005"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0006" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol>

0016In another aspect, the invention relates to a Nanobody (as defined herein), against vWF, which consist of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: i) CDR1 is an amino acid sequence chosen from the group consisting of: <tables id="tabl0004" num="0004"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>NYGMG</entry><entry>[SEQ ID NO: 15]</entry></row><row><entry>SYTLG</entry><entry>[SEQ ID NO: 16]</entry></row><row><entry>NYNMG</entry><entry>[SEQ ID NO: 17]</entry></row><row><entry>SSAMA</entry><entry>[SEQ ID NO: 18]</entry></row><row><entry>YYNTG</entry><entry>[SEQ ID NO: 19]</entry></row><row><entry>IGAMG</entry><entry>[SEQ ID NO: 20]</entry></row><row><entry>IGTMG</entry><entry>[SEQ ID NO: 21]</entry></row><row><entry>YNPMG</entry><entry>[SEQ ID NO: 22]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0007"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0008"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: ii) CDR2 is an amino acid sequence chosen from the group consisting of: <tables id="tabl0005" num="0005"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="44mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SISWSGTYTAYSDNVKG</entry><entry>[SEQ ID NO: 23]</entry></row><row><entry>GISWSGVSTDYAEFAKG</entry><entry>[SEQ ID NO: 24]</entry></row><row><entry>TSISWSGSYTAYADNVKG</entry><entry>[SEQ ID NO: 25]</entry></row><row><entry>SISWSGMSTYYTDSVKG</entry><entry>[SEQ ID NO: 26]</entry></row><row><entry>TITSGGRTSYADSVKG</entry><entry>[SEQ ID NO: 27]</entry></row><row><entry>AISWSGGLTYYADSVKG</entry><entry>[SEQ ID NO: 28]</entry></row><row><entry>TITSGGSTNYADPVKG</entry><entry>[SEQ ID NO: 29]</entry></row><row><entry>TITSGGSTNYADSVKG</entry><entry>[SEQ ID NO: 30]</entry></row><row><entry>AISRTGGSTYYARSVEG</entry><entry>[SEQ ID NO: 31]</entry></row><row><entry>AISRTGGSTYYPDSVEG</entry><entry>[SEQ ID NO: 32]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0009" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0010" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: iii) CDR3 is an amino acid sequence chosen from the group consisting of: <tables id="tabl0006" num="0006"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>QSRYRSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 33]</entry></row><row><entry>LGRYRSNWRNIGQYDY</entry><entry>[SEQ ID NO: 34]</entry></row><row><entry>QSRYSSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 35]</entry></row><row><entry>SNRYRTHTTQAMYNY</entry><entry>[SEQ ID NO: 36]</entry></row><row><entry>VVDGKRAP</entry><entry>[SEQ ID NO: 37]</entry></row><row><entry>NRRQKTVQMGERAYDY</entry><entry>[SEQ ID NO: 38]</entry></row><row><entry>NLKQGSYGYRFNDY</entry><entry>[SEQ ID NO: 39]</entry></row><row><entry>NLKQGDYGYRFNDY</entry><entry>[SEQ ID NO: 40]</entry></row><row><entry>AGVRAEDGRVRTLPSEYNF</entry><entry>[SEQ ID NO: 41]</entry></row><row><entry>AGVRAEDGRVRTLPSEYTF</entry><entry>[SEQ ID NO: 42]</entry></row><row><entry>AGVRAEDGRVRSLPSEYTF</entry><entry>[SEQ ID NO: 43]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0011" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0012" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol>

0017The Nanobodies against vWF as described above and as further described hereinbelow are also referred to herein as Nanobodies of the invention.

0018Of the Nanobodies of the invention, Nanobodies comprising one or more of the CDR's explicitly listed above are particularly preferred; Nanobodies comprising two or more of the CDR's explicitly listed above are more particularly preferred; and Nanobodies comprising three of the CDR's explicitly listed above are most particularly preferred.

0019In another aspect, the invention relates to a Nanobody against vWF, which consist of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), which is chosen from the group consisting of Nanobodies with the one of the following combinations of CDR1, CDR2 and CDR3, respectively: <ul id="ul0002" list-style="dash" compact="compact"><li><b>CDR1</b>:NYGMG;<b>CDR2</b>:SISWSGTYTAYSDNVKG; <b>CDR3</b>:QSRYRSNYYDHDDKYAY</li><li><b>CDR1</b>:SYTLG;<b>CDR2</b>:GISWSGVSTDYAEFAKG; <b>CDR3</b>:LGRYRSNWRNIGQYDY</li><li><b>CDR1</b>:NYGMG;<b>CDR2</b>:TSISWSGSYTAYADNVKG; <b>CDR3:</b>QSRYSSNYYDHDDKYAY</li><li><b>CDR1</b>:NYNMG;<b>CDR2</b>:SISWSGMSTYYTDSVKG; <b>CDR3</b>:SNRYRTHTTQAMYNY</li><li><b>CDR1</b>:SSAMA;<b>CDR2</b>:TITSGGRTSYADSVKG;<b>CDR3</b>:VVDGKRAP</li><li><b>CDR1</b>:YYNTG;<b>CDR2</b>:AISWSGGLTYYADSVKG; <b>CDR3</b>:NRRQKTVQMGERAYDY</li><li><b>CDR1</b>:IGAMG;<b>CDR2</b>:TITSGGSTNYADPVKG;<b>CDR3</b>:NLKQGSYGYRFNDY</li><li><b>CDR1</b>:IGAMG;<b>CDR2</b>:TITSGGSTNYADSVKG;<b>CDR3</b>:NLKQGSYGYRFNDY</li><li><b>CDR1</b>:IGAMG;<b>CDR2</b>:TITSGGSTNYADSVKG; <b>CDR3</b>:NLKQGDYGYRFNDY</li><li><b>CDR1</b>:IGTMG;<b>CDR2</b>:TITSGGSTNYADSVKG;<b>CDR3</b>:NLKQGDYGYRFNDY</li><li><b>CDR1</b>:YNPMG;<b>CDR2</b>:AISRTGGSTYYARSVEG; <b>CDR3</b>:AGVRAEDGRVRTLPSEYNF</li><li><b>CDR1</b>:YNPMG;<b>CDR2</b>:AISRTGGSTYYPDSVEG; <b>CDR3</b>:AGVRAEDGRVRTLPSEYTF</li><li><b>CDR1</b>:YNPMG;<b>CDR2</b>:AISRTGGSTYYPDSVEG; <b>CDR3</b>:AGVRAEDGRVRSLPSEYTF</li></ul>

0020In the Nanobodies of the invention that comprise the combinations of CDR's mentioned above, each CDR can be replaced by a CDR chosen from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the mentioned CDR's; in which <ol id="ol0013" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or chosen from the group consisting of amino acid sequences that have 3, 2 or only 1 (as indicated in the preceding paragraph) "amino acid difference(s)" (as defined herein) with the mentioned CDR(s) one of the above amino acid sequences, in which: <ol id="ol0014" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol>

0021However, of the Nanobodies of the invention that comprise the combinations of CDR's mentioned above, Nanobodies comprising one or more of the CDR's listed above are particularly preferred; Nanobodies comprising two or more of the CDR's listed above are more particularly preferred; and Nanobodies comprising three of the CDR's listed above are most particularly preferred. <tables id="tabl0007" num="0007"><table frame="all"><title><b>TABLE I: Preferred combinations of CDR's, of CDR's and framework sequences, and of CDR's and humanized FR's</b></title><tgroup cols="15"><colspec colnum="1" colname="col1" colwidth="10mm" /><colspec colnum="2" colname="col2" colwidth="6mm" /><colspec colnum="3" colname="col3" colwidth="30mm" /><colspec colnum="4" colname="col4" colwidth="6mm" /><colspec colnum="5" colname="col5" colwidth="10mm" /><colspec colnum="6" colname="col6" colwidth="6mm" /><colspec colnum="7" colname="col7" colwidth="27mm" /><colspec colnum="8" colname="col8" colwidth="6mm" /><colspec colnum="9" colname="col9" colwidth="29mm" /><colspec colnum="10" colname="col10" colwidth="6mm" /><colspec colnum="11" colname="col11" colwidth="42mm" /><colspec colnum="12" colname="col12" colwidth="6mm" /><colspec colnum="13" colname="col13" colwidth="42mm" /><colspec colnum="14" colname="col14" colwidth="6mm" /><colspec colnum="15" colname="col15" colwidth="17mm" /><thead><row><entry>CLONE</entry><entry>ID</entry><entry>FR1</entry><entry>ID</entry><entry>CDR1</entry><entry /><entry>FR2</entry><entry>ID</entry><entry>CCR1</entry><entry>ID</entry><entry>FR3</entry><entry /><entry>CDR3</entry><entry>ID</entry><entry>FR4</entry></row></thead><tbody><row><entry valign="bottom">12A5</entry><entry valign="bottom">122</entry><entry valign="bottom"><img file="EP3415535A1_D0001.tif" /></entry><entry valign="bottom">148</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">174</entry><entry valign="bottom"><img file="EP3415535A1_D0002.tif" /></entry><entry valign="bottom">200</entry><entry valign="bottom"><img file="EP3415535A1_D0003.tif" /></entry><entry valign="bottom">226</entry><entry valign="bottom"><img file="EP3415535A1_D0004.tif" /></entry><entry valign="bottom">252</entry><entry valign="bottom">NLKQGSYGYRFNDY</entry><entry valign="bottom">278</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B1</entry><entry valign="bottom">123</entry><entry valign="bottom"><img file="EP3415535A1_D0005.tif" /></entry><entry valign="bottom">149</entry><entry valign="bottom">NYGMG</entry><entry valign="bottom">175</entry><entry valign="bottom"><img file="EP3415535A1_D0006.tif" /></entry><entry valign="bottom">201</entry><entry valign="bottom"><img file="EP3415535A1_D0007.tif" /></entry><entry valign="bottom">227</entry><entry valign="bottom"><img file="EP3415535A1_D0008.tif" /></entry><entry valign="bottom">253</entry><entry valign="bottom"><img file="EP3415535A1_D0009.tif" /></entry><entry valign="bottom">279</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B6</entry><entry valign="bottom">124</entry><entry valign="bottom"><img file="EP3415535A1_D0010.tif" /></entry><entry valign="bottom">150</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">176</entry><entry valign="bottom"><img file="EP3415535A1_D0011.tif" /></entry><entry valign="bottom">202</entry><entry valign="bottom"><img file="EP3415535A1_D0012.tif" /></entry><entry valign="bottom">228</entry><entry valign="bottom"><img file="EP3415535A1_D0013.tif" /></entry><entry valign="bottom">254</entry><entry valign="bottom"><img file="EP3415535A1_D0014.tif" /></entry><entry valign="bottom">280</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12D11</entry><entry valign="bottom">125</entry><entry valign="bottom"><img file="EP3415535A1_D0015.tif" /></entry><entry valign="bottom">151</entry><entry valign="bottom">SSYTLG</entry><entry valign="bottom">177</entry><entry valign="bottom"><img file="EP3415535A1_D0016.tif" /></entry><entry valign="bottom">203</entry><entry valign="bottom"><img file="EP3415535A1_D0017.tif" /></entry><entry valign="bottom">229</entry><entry valign="bottom"><img file="EP3415535A1_D0018.tif" /></entry><entry valign="bottom">255</entry><entry valign="bottom"><img file="EP3415535A1_D0019.tif" /></entry><entry valign="bottom">281</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12-E3</entry><entry valign="bottom">126</entry><entry valign="bottom"><img file="EP3415535A1_D0020.tif" /></entry><entry valign="bottom">152</entry><entry valign="bottom">NYGMG</entry><entry valign="bottom">178</entry><entry valign="bottom"><img file="EP3415535A1_D0021.tif" /></entry><entry valign="bottom">204</entry><entry valign="bottom"><img file="EP3415535A1_D0022.tif" /></entry><entry valign="bottom">230</entry><entry valign="bottom"><img file="EP3415535A1_D0023.tif" /></entry><entry valign="bottom">256</entry><entry valign="bottom"><img file="EP3415535A1_D0024.tif" /></entry><entry valign="bottom">282</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12C9</entry><entry valign="bottom">127</entry><entry valign="bottom"><img file="EP3415535A1_D0025.tif" /></entry><entry valign="bottom">153</entry><entry valign="bottom">SSAMA</entry><entry valign="bottom">179</entry><entry valign="bottom"><img file="EP3415535A1_D0026.tif" /></entry><entry valign="bottom">205</entry><entry valign="bottom"><img file="EP3415535A1_D0027.tif" /></entry><entry valign="bottom">231</entry><entry valign="bottom"><img file="EP3415535A1_D0028.tif" /></entry><entry valign="bottom">257</entry><entry valign="bottom">VVDGKRAP</entry><entry valign="bottom">283</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">14F8</entry><entry valign="bottom">128</entry><entry valign="bottom"><img file="EP3415535A1_D0029.tif" /></entry><entry valign="bottom">154</entry><entry valign="bottom">YYNTG</entry><entry valign="bottom">180</entry><entry valign="bottom"><img file="EP3415535A1_D0030.tif" /></entry><entry valign="bottom">206</entry><entry valign="bottom"><img file="EP3415535A1_D0031.tif" /></entry><entry valign="bottom">232</entry><entry valign="bottom"><img file="EP3415535A1_D0032.tif" /></entry><entry valign="bottom">258</entry><entry valign="bottom"><img file="EP3415535A1_D0033.tif" /></entry><entry valign="bottom">284</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B4</entry><entry valign="bottom">129</entry><entry valign="bottom"><img file="EP3415535A1_D0034.tif" /></entry><entry valign="bottom">155</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">181</entry><entry valign="bottom"><img file="EP3415535A1_D0035.tif" /></entry><entry valign="bottom">207</entry><entry valign="bottom"><img file="EP3415535A1_D0036.tif" /></entry><entry valign="bottom">233</entry><entry valign="bottom"><img file="EP3415535A1_D0037.tif" /></entry><entry valign="bottom">259</entry><entry valign="bottom">NLKQGSYGYRFNDY</entry><entry valign="bottom">285</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12-E8</entry><entry valign="bottom">130</entry><entry valign="bottom"><img file="EP3415535A1_D0038.tif" /></entry><entry valign="bottom">156</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">182</entry><entry valign="bottom"><img file="EP3415535A1_D0039.tif" /></entry><entry valign="bottom">208</entry><entry valign="bottom"><img file="EP3415535A1_D0040.tif" /></entry><entry valign="bottom">234</entry><entry valign="bottom"><img file="EP3415535A1_D0041.tif" /></entry><entry valign="bottom">260</entry><entry valign="bottom">NLKQGDYGYRFN DY</entry><entry valign="bottom">286</entry><entry valign="bottom">WGQGTQVTVSS</entry></row></tbody></tgroup><tgroup cols="15"><colspec colnum="1" colname="col1" colwidth="10mm" /><colspec colnum="2" colname="col2" colwidth="6mm" /><colspec colnum="3" colname="col3" colwidth="30mm" /><colspec colnum="4" colname="col4" colwidth="6mm" /><colspec colnum="5" colname="col5" colwidth="10mm" /><colspec colnum="6" colname="col6" colwidth="6mm" /><colspec colnum="7" colname="col7" colwidth="27mm" /><colspec colnum="8" colname="col8" colwidth="6mm" /><colspec colnum="9" colname="col9" colwidth="29mm" /><colspec colnum="10" colname="col10" colwidth="6mm" /><colspec colnum="11" colname="col11" colwidth="42mm" /><colspec colnum="12" colname="col12" colwidth="6mm" /><colspec colnum="13" colname="col13" colwidth="42mm" /><colspec colnum="14" colname="col14" colwidth="6mm" /><colspec colnum="15" colname="col15" colwidth="17mm" /><thead><row><entry>CLONE</entry><entry>ID</entry><entry>FR1</entry><entry>ID</entry><entry>CDR1</entry><entry /><entry>FR2</entry><entry>ID</entry><entry>CDR1</entry><entry>ID</entry><entry>FR3</entry><entry /><entry>CDR3</entry><entry>ID</entry><entry>FR4</entry></row></thead><tbody><row><entry valign="bottom">12A6</entry><entry valign="bottom">131</entry><entry valign="bottom"><img file="EP3415535A1_D0042.tif" /></entry><entry valign="bottom">157</entry><entry valign="bottom">IGTMG</entry><entry valign="bottom">183</entry><entry valign="bottom"><img file="EP3415535A1_D0043.tif" /></entry><entry valign="bottom">209</entry><entry valign="bottom"><img file="EP3415535A1_D0044.tif" /></entry><entry valign="bottom">235</entry><entry valign="bottom"><img file="EP3415535A1_D0045.tif" /></entry><entry valign="bottom">261</entry><entry valign="bottom">NLKQGDYGYRFN DY</entry><entry valign="bottom">287</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12D8</entry><entry valign="bottom">132</entry><entry valign="bottom"><img file="EP3415535A1_D0046.tif" /></entry><entry valign="bottom">158</entry><entry valign="bottom">IGTMG</entry><entry valign="bottom">184</entry><entry valign="bottom"><img file="EP3415535A1_D0047.tif" /></entry><entry valign="bottom">210</entry><entry valign="bottom"><img file="EP3415535A1_D0048.tif" /></entry><entry valign="bottom">236</entry><entry valign="bottom"><img file="EP3415535A1_D0049.tif" /></entry><entry valign="bottom">262</entry><entry valign="bottom">NLKQGDYGYRFNDY</entry><entry valign="bottom">288</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2</entry><entry valign="bottom">133</entry><entry valign="bottom"><img file="EP3415535A1_D0050.tif" /></entry><entry valign="bottom">159</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">185</entry><entry valign="bottom"><img file="EP3415535A1_D0051.tif" /></entry><entry valign="bottom">211</entry><entry valign="bottom"><img file="EP3415535A1_D0052.tif" /></entry><entry valign="bottom">237</entry><entry valign="bottom"><img file="EP3415535A1_D0053.tif" /></entry><entry valign="bottom">263</entry><entry valign="bottom"><img file="EP3415535A1_D0054.tif" /></entry><entry valign="bottom">289</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12F2</entry><entry valign="bottom">134</entry><entry valign="bottom"><img file="EP3415535A1_D0055.tif" /></entry><entry valign="bottom">160</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">186</entry><entry valign="bottom"><img file="EP3415535A1_D0056.tif" /></entry><entry valign="bottom">212</entry><entry valign="bottom"><img file="EP3415535A1_D0057.tif" /></entry><entry valign="bottom">238</entry><entry valign="bottom"><img file="EP3415535A1_D0058.tif" /></entry><entry valign="bottom">264</entry><entry valign="bottom"><img file="EP3415535A1_D0059.tif" /></entry><entry valign="bottom">290</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">14H10</entry><entry valign="bottom">135</entry><entry valign="bottom"><img file="EP3415535A1_D0060.tif" /></entry><entry valign="bottom">161</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">187</entry><entry valign="bottom"><img file="EP3415535A1_D0061.tif" /></entry><entry valign="bottom">213</entry><entry valign="bottom"><img file="EP3415535A1_D0062.tif" /></entry><entry valign="bottom">239</entry><entry valign="bottom"><img file="EP3415535A1_D0063.tif" /></entry><entry valign="bottom">265</entry><entry valign="bottom"><img file="EP3415535A1_D0064.tif" /></entry><entry valign="bottom">291</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B6H1</entry><entry valign="bottom">136</entry><entry valign="bottom"><img file="EP3415535A1_D0065.tif" /></entry><entry valign="bottom">162</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">188</entry><entry valign="bottom"><img file="EP3415535A1_D0066.tif" /></entry><entry valign="bottom">214</entry><entry valign="bottom"><img file="EP3415535A1_D0067.tif" /></entry><entry valign="bottom">240</entry><entry valign="bottom"><img file="EP3415535A1_D0068.tif" /></entry><entry valign="bottom">266</entry><entry valign="bottom"><img file="EP3415535A1_D0069.tif" /></entry><entry valign="bottom">292</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B6H2</entry><entry valign="bottom">137</entry><entry valign="bottom"><img file="EP3415535A1_D0070.tif" /></entry><entry valign="bottom">163</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">189</entry><entry valign="bottom"><img file="EP3415535A1_D0071.tif" /></entry><entry valign="bottom">215</entry><entry valign="bottom"><img file="EP3415535A1_D0072.tif" /></entry><entry valign="bottom">241</entry><entry valign="bottom"><img file="EP3415535A1_D0073.tif" /></entry><entry valign="bottom">267</entry><entry valign="bottom"><img file="EP3415535A1_D0074.tif" /></entry><entry valign="bottom">293</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B6H3</entry><entry valign="bottom">138</entry><entry valign="bottom"><img file="EP3415535A1_D0075.tif" /></entry><entry valign="bottom">164</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">190</entry><entry valign="bottom"><img file="EP3415535A1_D0076.tif" /></entry><entry valign="bottom">216</entry><entry valign="bottom"><img file="EP3415535A1_D0077.tif" /></entry><entry valign="bottom">242</entry><entry valign="bottom"><img file="EP3415535A1_D0078.tif" /></entry><entry valign="bottom">268</entry><entry valign="bottom"><img file="EP3415535A1_D0079.tif" /></entry><entry valign="bottom">294</entry><entry valign="bottom">4 WGQGTQVTVSS</entry></row><row><entry valign="bottom">12B6H4</entry><entry valign="bottom">139</entry><entry valign="bottom"><img file="EP3415535A1_D0080.tif" /></entry><entry valign="bottom">165</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">191</entry><entry valign="bottom"><img file="EP3415535A1_D0081.tif" /></entry><entry valign="bottom">217</entry><entry valign="bottom"><img file="EP3415535A1_D0082.tif" /></entry><entry valign="bottom">243</entry><entry valign="bottom"><img file="EP3415535A1_D0083.tif" /></entry><entry valign="bottom">269</entry><entry valign="bottom"><img file="EP3415535A1_D0084.tif" /></entry><entry valign="bottom">295</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2H1</entry><entry valign="bottom">140</entry><entry valign="bottom"><img file="EP3415535A1_D0085.tif" /></entry><entry valign="bottom">166</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">192</entry><entry valign="bottom"><img file="EP3415535A1_D0086.tif" /></entry><entry valign="bottom">218</entry><entry valign="bottom"><img file="EP3415535A1_D0087.tif" /></entry><entry valign="bottom">244</entry><entry valign="bottom"><img file="EP3415535A1_D0088.tif" /></entry><entry valign="bottom">270</entry><entry valign="bottom"><img file="EP3415535A1_D0089.tif" /></entry><entry valign="bottom">296</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2H3</entry><entry valign="bottom">141</entry><entry valign="bottom"><img file="EP3415535A1_D0090.tif" /></entry><entry valign="bottom">167</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">193</entry><entry valign="bottom"><img file="EP3415535A1_D0091.tif" /></entry><entry valign="bottom">219</entry><entry valign="bottom"><img file="EP3415535A1_D0092.tif" /></entry><entry valign="bottom">245</entry><entry valign="bottom"><img file="EP3415535A1_D0093.tif" /></entry><entry valign="bottom">271</entry><entry valign="bottom"><img file="EP3415535A1_D0094.tif" /></entry><entry valign="bottom">297</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2H4</entry><entry valign="bottom">142</entry><entry valign="bottom"><img file="EP3415535A1_D0095.tif" /></entry><entry valign="bottom">168</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">194</entry><entry valign="bottom"><img file="EP3415535A1_D0096.tif" /></entry><entry valign="bottom">220</entry><entry valign="bottom"><img file="EP3415535A1_D0097.tif" /></entry><entry valign="bottom">246</entry><entry valign="bottom"><img file="EP3415535A1_D0098.tif" /></entry><entry valign="bottom">272</entry><entry valign="bottom"><img file="EP3415535A1_D0099.tif" /></entry><entry valign="bottom">298</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2H11</entry><entry valign="bottom">143</entry><entry valign="bottom"><img file="EP3415535A1_D0100.tif" /></entry><entry valign="bottom">169</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">195</entry><entry valign="bottom"><img file="EP3415535A1_D0101.tif" /></entry><entry valign="bottom">221</entry><entry valign="bottom"><img file="EP3415535A1_D0102.tif" /></entry><entry valign="bottom">247</entry><entry valign="bottom"><img file="EP3415535A1_D0103.tif" /></entry><entry valign="bottom">273</entry><entry valign="bottom"><img file="EP3415535A1_D0104.tif" /></entry><entry valign="bottom">299</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A2H13</entry><entry valign="bottom">144</entry><entry valign="bottom"><img file="EP3415535A1_D0105.tif" /></entry><entry valign="bottom">170</entry><entry valign="bottom">YNPMG</entry><entry valign="bottom">196</entry><entry valign="bottom"><img file="EP3415535A1_D0106.tif" /></entry><entry valign="bottom">222</entry><entry valign="bottom"><img file="EP3415535A1_D0107.tif" /></entry><entry valign="bottom">248</entry><entry valign="bottom"><img file="EP3415535A1_D0108.tif" /></entry><entry valign="bottom">274</entry><entry valign="bottom"><img file="EP3415535A1_D0109.tif" /></entry><entry valign="bottom">300</entry><entry valign="bottom">WGQGTL VTVSS</entry></row><row><entry valign="bottom">12A5H1</entry><entry valign="bottom">145</entry><entry valign="bottom"><img file="EP3415535A1_D0110.tif" /></entry><entry valign="bottom">171</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">197</entry><entry valign="bottom"><img file="EP3415535A1_D0111.tif" /></entry><entry valign="bottom">223</entry><entry valign="bottom"><img file="EP3415535A1_D0112.tif" /></entry><entry valign="bottom">249</entry><entry valign="bottom"><img file="EP3415535A1_D0113.tif" /></entry><entry valign="bottom">275</entry><entry valign="bottom">NLKQGSYGYRFNDY</entry><entry valign="bottom">301</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A5H2</entry><entry valign="bottom">146</entry><entry valign="bottom"><img file="EP3415535A1_D0114.tif" /></entry><entry valign="bottom">172</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">198</entry><entry valign="bottom"><img file="EP3415535A1_D0115.tif" /></entry><entry valign="bottom">224</entry><entry valign="bottom"><img file="EP3415535A1_D0116.tif" /></entry><entry valign="bottom">250</entry><entry valign="bottom"><img file="EP3415535A1_D0117.tif" /></entry><entry valign="bottom">276</entry><entry valign="bottom">NLKQGSYGYRFNDY</entry><entry valign="bottom">302</entry><entry valign="bottom">WGQGTQVTVSS</entry></row><row><entry valign="bottom">12A5H3</entry><entry valign="bottom">147</entry><entry valign="bottom"><img file="EP3415535A1_D0118.tif" /></entry><entry valign="bottom">173</entry><entry valign="bottom">IGAMG</entry><entry valign="bottom">199</entry><entry valign="bottom"><img file="EP3415535A1_D0119.tif" /></entry><entry valign="bottom">225</entry><entry valign="bottom"><img file="EP3415535A1_D0120.tif" /></entry><entry valign="bottom">251</entry><entry valign="bottom"><img file="EP3415535A1_D0121.tif" /></entry><entry valign="bottom">277</entry><entry valign="bottom">NLKQGSYGYRFNDY</entry><entry valign="bottom">303</entry><entry valign="bottom">WGQGTQVTVSS</entry></row></tbody></tgroup></table></tables>

0022Thus, in the Nanobodies of the invention, at least one of the CDR1, CDR2 and CDR3 sequences present is suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I; or from the group of CDR1, CDR2 and CDR3 sequences, respectively, that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% "sequence identity" (as defined herein) with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I; and/or from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I. In this context, by "suitably chosen" is meant that, as applicable, a CDR1 sequence is chosen from suitable CDR1 sequences (i.e. as defined herein), a CDR2 sequence is chosen from suitable CDR2 sequences (i.e. as defined herein), and a CDR3 sequence is chosen from suitable CDR3 sequence (i.e. as defined herein), respectively.

0023In particular, in the Nanobodies of the invention, at least the CDR3 sequence present is suitably chosen from the group consisting of the CDR3 sequences listed in Table I or from the group of CDR3 sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the CDR3 sequences listed in Table I; and/or from the group consisting of the CDR3 sequences that have 3, 2 or only 1 amino acid difference(s) with at least one of the CDR3 sequences listed in Table I.

0024Preferably, in the Nanobodies of the invention, at least two of the CDR1, CDR2 and CDR3 sequences present are suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I or from the group consisting of CDR1, CDR2 and CDR3 sequences, respectively, that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I; and/or from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, that have 3, 2 or only 1 "amino acid difference(s)" with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I.

0025In particular, in the Nanobodies of the invention, at least the CDR3 sequence present is suitably chosen from the group consisting of the CDR3 sequences listed in Table I or from the group of CDR3 sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the CDR3 sequences listed in Table I, respectively; and at least one of the CDR1 and CDR2 sequences present is suitably chosen from the group consisting of the CDR1 and CDR2 sequences, respectively, listed in Table I or from the group of CDR1 and CDR2 sequences, respectively, that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the CDR1 and CDR2 sequences, respectively, listed in Table I; and/or from the group consisting of the CDR1 and CDR2 sequences, respectively, that have 3, 2 or only 1 amino acid difference(s) with at least one of the CDR1 and CDR2 sequences, respectively, listed in Table I.

0026Most preferably, in the Nanobodies of the invention, all three CDR1, CDR2 and CDR3 sequences present are suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I or from the group of CDR1, CDR2 and CDR3 sequences, respectively, that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I; and/or from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, that have 3, 2 or only 1 amino acid difference(s) with at least one of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I.

0027Even more preferably, in the Nanobodies of the invention, at least one of the CDR1, CDR2 and CDR3 sequences present is suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I. Preferably, in this embodiment, at least one or preferably both of the other two CDR sequences present are suitably chosen from CDR sequences that that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the corresponding CDR sequences, respectively, listed in Table I; and/or from the group consisting of the CDR sequences that have 3, 2 or only 1 amino acid difference(s) with at least one of the corresponding sequences, respectively, listed in Table I.

0028In particular, in the Nanobodies of the invention, at least the CDR3 sequence present is suitably chosen from the group consisting of the CDR3 listed in Table I. Preferably, in this embodiment, at least one and preferably both of the CDR1 and CDR2 sequences present are suitably chosen from the groups of CDR1 and CDR2 sequences, respectively, that that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the CDR1 and CDR2 sequences, respectively, listed in listed in Table I; and/or from the group consisting of the CDR1 and CDR2 sequences, respectively, that have 3, 2 or only 1 amino acid difference(s) with at least one of the CDR1 and CDR2 sequences, respectively, listed in Table I.

0029Even more preferably, in the Nanobodies of the invention, at least two of the CDR1, CDR2 and CDR3 sequences present are suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I. Preferably, in this embodiment, the remaining CDR sequence present are suitably chosen from the group of CDR sequences that that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the corresponding CDR sequences listed in Table I; and/or from the group consisting of CDR sequences that have 3, 2 or only 1 amino acid difference(s) with at least one of the corresponding sequences listed in Table I.

0030In particular, in the Nanobodies of the invention, at least the CDR3 sequence is suitably chosen from the group consisting of the CDR3 sequences listed in Table I, and either the CDR1 sequence or the CDR2 sequence is suitably chosen from the group consisting of the CDR1 and CDR2 sequences, respectively, listed in Table I. Preferably, in this embodiment, the remaining CDR sequence present are suitably chosen from the group of CDR sequences that that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with at least one of the corresponding CDR sequences listed in Table I; and/or from the group consisting of CDR sequences that have 3, 2 or only 1 amino acid difference(s) with the corresponding CDR sequences listed in Table I.

0031Even more preferably, in the Nanobodies of the invention, all three CDR1, CDR2 and CDR3 sequences present are suitably chosen from the group consisting of the CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I.

0032Also, generally, the combinations of CDR's listed in Table I (i.e. those mentioned on the same line in Table I) are preferred. Thus, it is generally preferred that, when a CDR in a Nanobody of the invention is a CDR sequence mentioned in Table I or is suitably chosen from the group of CDR sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with a CDR sequence listed in Table I; and/or from the group consisting of CDR sequences that have 3, 2 or only 1 amino acid difference(s) with a CDR sequence listed in Table I, that at least one and preferably both of the other CDR's are suitably chosen from the CDR sequences that belong to the same combination in Table I (i.e. mentioned on the same line in Table I) or are suitably chosen from the group of CDR sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the CDR sequence(s) belonging to the same combination and/or from the group consisting of CDR sequences that have 3, 2 or only 1 amino acid difference(s) with the CDR sequence(s) belonging to the same combination.The other preferences indicated in the above paragraphs also apply to the combinations of CDR's mentioned in Table I.

0033Thus, by means of non-limiting examples, a Nanobody of the invention can for example comprise a CDR1 sequence that has more than 80 % sequence identity with one of the CDR1 sequences mentioned in Table I, a CDR2 sequence that has 3, 2 or 1 amino acid difference with one of the CDR2 sequences mentioned in Table I (but belonging to a different combination), and a CDR3 sequence.

0034Some preferred Nanobodies of the invention may for example comprise: (1) a CDR1 sequence that has more than 80 % sequence identity with one of the CDR1 sequences mentioned in Table I; a CDR2 sequence that has 3, 2 or 1 amino acid difference with one of the CDR2 sequences mentioned in Table I (but belonging to a different combination); and a CDR3 sequence that has more than 80 % sequence identity with one of the CDR3 sequences mentioned in Table I (but belonging to a different combination); or (2) a CDR1 sequence that has more than 80 % sequence identity with one of the CDR1 sequences mentioned in Table I; a CDR2 sequence, and one of the CDR3 sequences listed in Table I; or (3) a CDR1 sequence; a CDR2 sequence that has more than 80% sequence identity with one of the CDR2 sequence listed in Table I; and a CDR3 sequence that has 3, 2 or 1 amino acid differences with the CDR3 sequence mentioned in Table I that belongs to the same combination as the CDR2 sequence.

0035Some particularly preferred Nanobodies of the invention may for example comprise: (1) a CDR1 sequence that has more than 80 % sequence identity with one of the CDR1 sequences mentioned in Table I; a CDR2 sequence that has 3, 2 or I amino acid difference with the CDR2 sequence mentioned in Table I that belongs to the same combination; and a CDR3 sequence that has more than 80 % sequence identity with the CDR3 sequence mentioned in Table I that belongs to the same combination; (2) a CDR1 sequence; a CDR 2 listed in Table I and a CDR3 sequence listed in Table I (in which the CDR2 sequence and CDR3 sequence may belong to different combinations).

0036Some even more preferred Nanobodies of the invention may for example comprise: (1) a CDR1 sequence that has more than 80 % sequence identity with one of the CDR1 sequences mentioned in Table I; the CDR2 sequence listed in Table I that belongs to the same combination; and a CDR3 sequence mentioned in Table I that belongs to a different combination; or (2) a CDR1 sequence mentioned in Table I; a CDR2 sequence that has 3, 2 or 1 amino acid differences with the CDR2 sequence mentioned in Table I that belongs to the same combination; and more than 80% sequence identity with the CDR3 sequence listed in Table I that belongs to same different combination.

0037Particularly preferred Nanobodies of the invention may for example comprise a CDR1 sequence mentioned in Table I, a CDR2 sequence that has more than 80 % sequence identity with the CDR2 sequence mentioned in Table I that belongs to the same combination; and the CDR3 sequence mentioned in Table I that belongs to the same.

0038In the most preferred in the Nanobodies of the invention, the CDR1, CDR2 and CDR3 sequences present are suitably chosen from the one of the combinations of CDR1, CDR2 and CDR3 sequences, respectively, listed in Table I.

0039Preferably, when a CDR sequence is suitably chosen from the group of CDR sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the CDR sequences listed in Table I; and/or when a CDR sequence is suitably chosen from the group consisting of CDR sequences that have 3, 2 or only 1 amino acid difference(s) with one of the CDR sequences listed in Table I: <ol id="ol0015" compact="compact"><li>i) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>ii) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the CDR sequence listed in Table 1.</li></ol>

0040According to a non-limiting but preferred embodiment of the invention, the CDR sequences in the the Nanobodies of the invention are as defined above and are also such that the Nanobody of the invention binds to vWF with an dissociation constant (K_D) of 10^-5 to 10^-12 moles/liter (M) or less, and preferably 10^-7 to 10^-12 moles/liter (M) or less and more preferably 10^-8 to 10^-12 moles/liter (M), and/or with an association constant (K_A) of at least 10⁷ M^-1, preferably at least 10⁸ M^-1, more preferably at least 10⁹ M^-1, such as at least 10¹² M^-1; and in particular with a K_D less than 500 nM, preferably less than 200 nM, more preferably less than 10 nM, such as less than 500 pM. The K_D and K_A values of the Nanobody of the invention against vWF can be determined in a manner known per se, for example using the assay described herein. More generally, the Nanobodies described herein preferably have a dissociation constant with respect to vWF that is as described in this paragraph.

0041In another aspect, the invention relates to a Nanobody with an amino acid sequence that is chosen from the group consisting of SEQ ID NO's: 60 to 73 and SEQ ID NO's: 86 to 97 or from the group consisting of from amino acid sequences that have more than 80%, preferably more than 90%, more preferably more than 95%, such as 99% or more "sequence identity" (as defined herein) with one or more of the amino acid sequences of SEQ ID NO's: 60 to 73 and SEQ ID NO's: 86 to 97, which amino acid sequences most preferably have framework sequences that are as further defined below under the general description of the framework sequences of Nanobodies.

0042According to a specific, but non-limiting embodiment, the latter amino acid sequences have been "humanized", as further described below.

0043Most preferably, the Nanobodies of the invention are chosen from the group consisting of SEQ ID NO's: 60 to 73 and SEQ ID NO's: 86 to 97, of which the "humanized" Nanobodies of SEQ ID NO's: 86 to 97 may be particularly preferred.

0044Nanobodies that are particular preferred according to the invention is Nanobody 12B6 (SEQ ID NO: 62) and homologues and variants thereof, and in particular humanized variants thereof. Some particularly preferred, but non-limiting homologues and (humanized) variants are for example Nanobodies 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73) and humanized variants thereof, such as 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and 12A2H13 (SEQ ID NO: 94).

0045Particularly preferred in the invention is Nanobody 12A2 (SEQ ID NO: 71) and homologues and variants thereof, and in particular humanized variants thereof. Some particularly preferred, but non-limiting homologues and (humanized) variants are for example Nanobodies 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and 12A2H13 (SEQ ID NO: 94), of which Nanobody 12A2H1 (SEQ ID NO: 90) is in particular preferred.

0046Thus, one preferred but non-limiting aspect of the invention relates to aNanobody against Von Willebrand Factor (vWF), said Nanobody consisting of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: <ol id="ol0016" compact="compact"><li>a) CDR1 comprises or essentially consists of: <ul id="ul0003" list-style="dash" compact="compact"><li>the amino acid sequence YNPMG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence YNPMG;</li></ul> and</li><li>b) CDR2 comprises or essentially consists of: <ul id="ul0004" list-style="dash" compact="compact"><li>the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> and</li><li>c) CDR3 comprises or essentially consists of: <ul id="ul0005" list-style="dash" compact="compact"><li>the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequences that has only 1 amino acid difference with the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul></li></ol>

0047In particular, the invention relates to such a Nanobody, in which: <ul id="ul0006" list-style="dash" compact="compact"><li>CDR1 comprises or essentially consists of the amino acid sequence YNPMG;</li></ul> or in which: <ul id="ul0007" list-style="dash" compact="compact"><li>CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> or in which <ul id="ul0008" list-style="dash" compact="compact"><li>CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul>

0048For example, the invention relates to such Nanobodies, in which: <ul id="ul0009" list-style="dash" compact="compact"><li>CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF;</li></ul> or in which: <ul id="ul0010" list-style="dash" compact="compact"><li>CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> or in which: <ul id="ul0011" list-style="dash" compact="compact"><li>CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF</li></ul>

0049In one aspect, the invention relates to such a Nanobody, in which CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF.

0050The invention also relates to humanized variants of such a Nanobody. Some preferred, but non-limiting humanizing substitutions will be described herein, or will be clear to the skilled person by comparing the corresponding non-humanized and humanized Nanobodies disclosed herein. Some particularly useful humanizing substitutions are one or more of those present in the humanized variants of 12A2 (as will be clear to the skilled person from a comparison of the sequences of 12A2H1 (SEQ ID NO: 90) with the corresponding humanized sequences of 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and 12A2H13 (SEQ ID NO: 94).

0051Anotherone preferred but non-limiting aspect of the invention relates to aNanobody against Von Willebrand Factor (vWF), said Nanobody consisting of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: <ul id="ul0012" list-style="none" compact="compact"><li>d) CDR1 is: <ul id="ul0013" list-style="dash" compact="compact"><li>the amino acid sequence YNPMG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence YNPMG;</li></ul> and</li><li>e) CDR2 is: <ul id="ul0014" list-style="dash" compact="compact"><li>the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> and</li><li>f) CDR3 is: <ul id="ul0015" list-style="dash" compact="compact"><li>the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequences that has only 1 amino acid difference with the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul></li></ul>

0052In particular, the invention relates to such a Nanobody, in which: <ul id="ul0016" list-style="dash" compact="compact"><li>CDR1 is the amino acid sequence YNPMG;</li></ul> or in which: <ul id="ul0017" list-style="dash" compact="compact"><li>CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG; or in which</li><li>CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul>

0053For example, the invention relates to such Nanobodies, in which: <ul id="ul0018" list-style="dash" compact="compact"><li>CDR1 is the amino acid sequence YNPMG; and CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF;</li></ul> or in which: <ul id="ul0019" list-style="dash" compact="compact"><li>CDR1 is the amino acid sequence YNPMG; and CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> or in which: <ul id="ul0020" list-style="dash" compact="compact"><li>CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG; and CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF</li></ul>

0054In one aspect, the invention relates to such a Nanobody, in which CDR1 is the amino acid sequence YNPMG; and CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF.

0055The invention also relates to humanized variants of such a Nanobody. Some preferred, but non-limiting humanizing substitutions will be described herein, or will be clear to the skilled person by comparing the corresponding non-humanized and humanized Nanobodies disclosed herein. Some particularly useful humanizing substitutions are one or more of those present in the humanized variants of 12A2 (as will be clear to the skilled person from a comparison of the sequences of 12A2H1 (SEQ ID NO: 90) with the corresponding humanized sequences of 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and 12A2H13 (SEQ ID NO: 94).

0056The Nanobodies described herein may be GLEW-class Nanobodies, "103 P, R or S"-class Nanobodies or "KERE-class Nanobodies" (all as described herein). In particular, the Nanobodies described herein may be KERE-class Nanobodies, although the invention is not limited thereto.

0057In another aspect, the invention relates to a Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the Nanobodies from the group consisting of SEQ ID NO's 60-73 and SEQ ID NO's 86-97.

0058In particular, the invention relates to a Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the Nanobodies 12B6 (SEQ ID NO: 62); 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73); 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94).

0059More in particular, the invention relates to a Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the Nanobodies 12A2 (SEQ ID NO: 71); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94).

0060Even more in particular, the invention relates to a Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with the Nanobody 12A2H1 (SEQ ID NO: 90).

0061The invention also relates to humanized variants of such Nanobodies. Some preferred, but non-limiting humanizing substitutions will be described herein, or will be clear to the skilled person by comparing the corresponding non-humanized and humanized Nanobodies disclosed herein. Some particularly useful humanizing substitutions are one or more of those present in the humanized variants of 12A2 (as will be clear to the skilled person from a comparison of the sequences of 12A2H1 (SEQ ID NO: 90) with the corresponding humanized sequences of 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and 12A2H13 (SEQ ID NO: 94).

0062The invention also relates to a Nanobody that is chosen from the group consisting of the Nanobodies of SEQ ID NO's 60-73 and SEQ ID NO's 86-97.

0063In particular, the invention relates to a Nanobody that is chosen from the group consisting of the Nanobodies 12B6 (SEQ ID NO: 62); 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73); 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94).

0064More in particular, the invention relates to a Nanobody that is chosen from the group consisting of the Nanobodies 12A2 (SEQ ID NO: 71); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). A particularly useful Nanobody is Nanobody 12A2H1 (SEQ ID NO:90).

0065The Nanobodies described herein preferably have framework sequences that are as further described herein. Some particularly preferred framework sequences (FR1, FR2, FR3 and FR4, respectively) are those of Nanobody 12A2 and its humanized variants; and framework sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said framework sequences; and and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of said framework sequences (in which any amino acid substitution is preferably a conservative amino acid substitution; and/or in which said amino acid sequence preferably contains amino acid substitutions and no more than 3 amino acid deletions or no more than 3 amino acid insertions). Nanobodies against vWF with such framework sequences form a further aspect of the invention.

0066In particular, the invention relates to a Nanobody against vWF, in which FR1 is SEQ ID NO: 140; FR2 is SEQ ID NO: 192; FR3 is SEQ ID 244; and FR4 is SEQ ID NO: 296; or framework sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said framework sequences; and and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of said framework sequences (in which any amino acid substitution is preferably a conservative amino acid substitution; and/or in which said amino acid sequence preferably contains amino acid substitutions and no more than 3 amino acid deletions or no more than 3 amino acid insertions).

0067More in particular, the invention relates to a Nanobody against vWF, in which FR1 is SEQ ID NO: 140; FR2 is SEQ ID NO: 192; FR3 is SEQ ID 244; and FR4 is SEQ ID NO: 296.

0068In another aspect, the invention relates to a polypeptide that comprises or essentially consists of at least one Nanobody against vWF as defined herein. Such polypeptides are also referred to herein as "polypeptides of the invention" and may be as further described hereinbelow and/or as generally described in <patcit id="pcit0019" dnum="WO02062551A"><text>WO 02/062551</text></patcit> for the Nanobodies disclosed therein, and may for example be multivalent polypeptides or multispecific polypeptides, again as further described hereinbelow.

0069Preferably, a polypeptide of the invention is either bivalent or trivalent (i.e. comprising two or three Nanobodies of the invention, respectively, optionally linked via one or two linkers as defined herein, respectively) or a multispecific polypeptide, comprising one or two, and preferably two, Nanobodies of the invention and at least one Nanobody directed against a serum protein, and in particular against a human serum protein, such as against human serum albumin.

0070In one preferred, but non-limiting embodiments, the Nanobodies of the invention present in the polypeptides of the invention are chosen from the group consisting of SEQ ID NO's: 60 to 73 and SEQ ID NO's: 86 to 97, and in particular from the "humanized" Nanobodies of SEQ ID NO's 86 to 97. The Nanobodies against human serum albumin present in the polypeptides of the invention are preferably as defined herein, and are more preferably chosen from the group consisting of SEQ ID NO's: 107 to 121, and in particular from the "humanized" Nanobodies against human serum albumin of SEQ ID NO's 114-121.

0071Some preferred, but non-limiting examples of polypeptides of the invention are the polypeptides of SEQ ID NO's: 74 to 82 and the polypeptides of SEQ ID NO's 98-106. Other polypeptides of the invention may for example be chosen from the group consisting of amino acid sequences that have more than 80%, preferably more than 90%, more preferably more than 95%, such as 99% or more "sequence identity" (as defined herein) with one or more of the amino acid sequences of SEQ ID NO's: 74 to 82 and/or SEQ ID NO's 98 to 106, in which the Nanobodies comprised within said amino acid sequences are preferably as defined herein.

0072According to one aspect of the invention, the Nanobodies, proteins and polypeptides described herein have essentially no influence on the cleavage of ULvWF by ADAMTS-13. In particular, when the Nanobodies, proteins and polypeptides described herein are used at the doses described herein, the cleavage of ULvWF by ADAMTS-13 (either in vivo upon administration and/or as measured using a suitable assay, such as the assay described herein), essentially does not reduce or inhibit the cleavage of ULvWF by ADAMTS-13, i.e. by not more than 50%, preferably not more than 20%, even more preferably not more than 10%, such as less than 5% or essentially not at all). Thus, one further aspect of the invention relates to a Nanobody, protein or polypeptide, and in particular a Nanobody, protein or polypeptide as described herein, that essentially does not reduce or inhibit the cleavage of ULvWF by ADAMTS-13.

0073In another aspect, the invention relates to a nucleic acid that encodes a Nanobody of the invention and/or a polypeptide of the invention. Such a nucleic acid will also be referred to below as a "nucleic acid of the invention" and may for example be in the form of a genetic construct, as defined herein.

0074In another aspect, the invention relates to host or host cell that expresses or is capable of expressing a Nanobody of the invention and/or a polypeptide of the invention; and/or that contains a nucleic acid encoding a Nanobody of the invention and/or a polypeptide of the invention. Such a host or a host cell may also be analogous to the hosts and host cells described in <patcit id="pcit0020" dnum="WO02062551A"><text>WO 02/062551</text></patcit>, but expressing or capable of expressing a Nanobody of the invention and/or a polypeptide of the invention and/or containing a nucleic acid as described herein.

0075The invention further relates to a product or composition containing or comprising a Nanobody of the invention, a polypeptide of the invention; and/or a nucleic acid of the invention. Such a product or composition may for example be a pharmaceutical composition (as described below) or a product or composition for diagnostic use (as also described below). Such a product or composition may also be analogous to the products and compositions described in <patcit id="pcit0021" dnum="WO02062551A"><text>WO 02/062551</text></patcit>, but containing or comprising a Nanobody of the invention, a polypeptide of the invention or a nucleic acid of the invention.

0076The invention further relates to methods for preparing or generating the Nanobodies, polypeptides, nucleic acids, host cells, products and compositions as described herein, which methods are as further described below. Also, generally, the Nanobodies, polypeptides, nucleic acids, host cells, products and compositions described herein may also be prepared and used in a manner analogous to the manner described in <patcit id="pcit0022" dnum="WO02062551A"><text>WO 02/062551</text></patcit>.

0077The invention further relates to applications and uses of the above Nanobodies, polypeptides, nucleic acids, host cells, products and compositions described herein, which applications and uses include, but are not limited to, the applications and uses described hereinbelow and/or the further uses and applications for Nanobodies against vWF and/or for polypeptides containing the same in <patcit id="pcit0023" dnum="WO02062551A"><text>WO 02/062551</text></patcit>.

0078Other aspects, embodiments, advantages and applications of the invention will become clear from the further description hereinbelow.

Detailed description of the invention

0079The above and other aspects and embodiments of the invention will become clear from the further description hereinbelow, in which: a) Unless indicated or defined otherwise, all terms used have their usual meaning in the art, which will be clear to the skilled person. Reference is for example made to the standard handbooks, such as <nplcit id="ncit0001" npl-type="b"><text>Sambrook et al, "Molecular Cloning: A Laboratory Manual" (2nd.Ed.), Vols. 1-3, Cold Spring Harbor Laboratory Press (1989</text></nplcit>); <nplcit id="ncit0002" npl-type="b"><text>F. Ausubel et al, eds., "Current protocols in molecular biology", Green Publishing and Wiley Interscience, New York (1987</text></nplcit>); <nplcit id="ncit0003" npl-type="b"><text>Roitt et al., "Immunology" (6th. Ed.), Mosby/Elsevier, Edinburgh (2001</text></nplcit>); and <nplcit id="ncit0004" npl-type="b"><text>Janeway et al., "Immunobiology" (6th Ed.), Garland Science Publishing/Churchill Livingstone, New York (2005</text></nplcit>), as well as to the general background art cited above; b) Unless indicated otherwise, the term <i>"immunoglobulin sequence"</i> - whether it used herein to refer to a heavy chain antibody or to a conventional 4-chain antibody - is used as a general term to include both the full-size antibody, the individual chains thereof, as well as all parts, domains or fragments thereof (including but not limited to antigen-binding domains or fragments such as V_HH domains or V_H/V_L domains, respectively). In addition, the term <i>"sequence"</i> as used herein (for example in terms like "immunoglobulin sequence", "antibody sequence", "variable domain sequence", "V_HH sequence" or "protein sequence"), should generally be understood to include both the relevant amino acid sequence as well as nucleic acid sequences or nucleotide sequences encoding the same, unless the context requires a more limited interpretation: c) Unless indicated otherwise, all methods, steps, techniques and manipulations that are not specifically described in detail can be performed and have been performed in a manner known per se, as will be clear to the skilled person. Reference is for example again made to the standard handbooks, to the general background art referred to above and to the further references cited therein; d) Amino acid residues will be indicated according to the standard three-letter or one-letter amino acid code, as mentioned in Table 1; <tables id="tabl0008" num="0008"><table frame="all"><title><b>Table 1: one-letter and three-letter amino acid code</b></title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="56mm" /><colspec colnum="2" colname="col2" colwidth="52mm" /><colspec colnum="3" colname="col3" colwidth="31mm" /><colspec colnum="4" colname="col4" colwidth="28mm" /><tbody><row><entry morerows="7">Nonpolar, uncharged (at pH 6,0 - 7.0)⁽³⁾</entry><entry>Alanine</entry><entry>Ala</entry><entry>A</entry></row><row><entry>Valine</entry><entry>Val</entry><entry>V</entry></row><row><entry>Leucine</entry><entry>Leu</entry><entry>L</entry></row><row><entry>Isoleucine</entry><entry>Ile</entry><entry>I</entry></row><row><entry>Phenylalanine</entry><entry>Phe</entry><entry>F</entry></row><row><entry>Methionine⁽¹⁾</entry><entry>Met</entry><entry>M</entry></row><row><entry>Tryptophan</entry><entry>Trp</entry><entry>W</entry></row><row><entry>Proline</entry><entry>Pro</entry><entry>P</entry></row><row><entry morerows="6">Polar, uncharged (at pH 6,0-7,0)</entry><entry>Glycine⁽²⁾</entry><entry>Gly</entry><entry>G</entry></row><row><entry>Serine</entry><entry>Ser</entry><entry>S</entry></row><row><entry>Threonine</entry><entry>Thr</entry><entry>T</entry></row><row><entry>Cysteine</entry><entry>Cys</entry><entry>C</entry></row><row><entry>Asparagine</entry><entry>Asn</entry><entry>N</entry></row><row><entry>Glutamine</entry><entry>Gln</entry><entry>Q</entry></row><row><entry>Tyrosine</entry><entry>Tyr</entry><entry>Y</entry></row><row><entry morerows="4">Polar, charged (at pH 6,0-7.0)</entry><entry>Lysine</entry><entry>Lys</entry><entry>K</entry></row><row><entry>Arginine</entry><entry>Arg</entry><entry>R</entry></row><row><entry>Histidine⁽⁴⁾</entry><entry>His</entry><entry>H</entry></row><row><entry>Aspartate</entry><entry>Asp</entry><entry>D</entry></row><row><entry>Glutamate</entry><entry>Glu</entry><entry>E</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">Notes:</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">(1) Sometimes also considered to be a polar uncharged amino acid.</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">(2) Sometimes also considered to be a nonpolar uncharged amino acid.</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">(3) As will be clear to the skilled person, the fact that an amino acid residue is referred to in this Table as being either charged or uncharged at pH 6,0 to 7,0 does not reflect in any way on the charge said amino acid residue may have at a pH lower than 6,0 and/or at a pH higher than 7,0; the amino acid residues mentioned in the Table can be either charged and/or uncharged at such a higher or lower pH, as will be clear to the skilled person.</entry></row><row><entry namest="col1" nameend="col4" align="left">(4) As is known in the art, the charge of a His residue is greatly dependant upon even small shifts in pH, but a His residu can generally be considered essentially uncharged at a pH of about 6,5.</entry></row></tbody></tgroup></table></tables> e) For the purposes of comparing two or more nucleotide sequences, the percentage of <i>"sequence identity"</i> between a first nucleotide sequence and a second nucleotide sequence may be calculated by dividing [<i>the number of nucleotides in the first nucleotide sequence that are identical to the nucleotides at the corresponding positions in the second nucleotide sequence</i>] by [<i>the total number of nucleotides in the first nucleotide sequence</i>] and multiplying by [100%], in which each deletion, insertion, substitution or addition of a nucleotide in the second nucleotide sequence - compared to the first nucleotide sequence - is considered as a difference at a single nucleotide (position). Alternatively, the degree of sequence identity between two or more nucleotide sequences may be calculated using a known computer algorithm for sequence alignment such as NCBI Blast v2.0, using standard settings. Some other techniques, computer algorithms and settings for determining the degree of sequence identity are for example described in <patcit id="pcit0024" dnum="WO04037999A"><text>WO 04/037999</text></patcit>, <patcit id="pcit0025" dnum="EP0967284A"><text>EP 0 967 284</text></patcit>, <patcit id="pcit0026" dnum="EP1085089A"><text>EP 1085 089</text></patcit>, <patcit id="pcit0027" dnum="WO0055318A"><text>WO 00/55318</text></patcit>, <patcit id="pcit0028" dnum="WO0078972A"><text>WO 00/78972</text></patcit>, <patcit id="pcit0029" dnum="WO9849185A"><text>WO 98/49185</text></patcit> and <patcit id="pcit0030" dnum="GB2357768A"><text>GB 2 357 768-A</text></patcit>. Usually, for the purpose of determining the percentage of "sequence identity" between two nucleotide sequences in accordance with the calculation method outlined hereinabove, the nucleotide sequence with the greatest number of nucleotides will be taken as the "first" nucleotide sequence, and the other nucleotide sequence will be taken as the "second" nucleotide sequence; f) For the purposes of comparing two or more amino acid sequences, the percentage of <i>"sequence identity"</i> between a first amino acid sequence and a second amino acid sequence may be calculated by dividing <i>[the number of amino acid residues in the first amino acid sequence that are identical to the amino acid residues at the corresponding positions in the second amino acid sequence</i>] by [<i>the total number of nucleotides in the first amino acid sequence</i>] and multiplying by [<i>100%</i>], in which each deletion, insertion, substitution or addition of an amino acid residue in the second amino acid sequence - compared to the first amino acid sequence - is considered as a difference at a single amino acid residue (position), i.e. as an <i>"amino acid difference"</i> as defined herein.

0080Alternatively, the degree of sequence identity between two amino acid sequences may be calculated using a known computer algorithm, such as those mentioned above for determining the degree of sequence identity for nucleotide sequences, again using standard settings.

0081Usually, for the purpose of determining the percentage of "sequence identity" between two amino acid sequences in accordance with the calculation method outlined hereinabove, the amino acid sequence with the greatest number of amino acid residues will be taken as the "first" amino acid sequence, and the other amino acid sequence will be taken as the "second" amino acid sequence.

0082Also, in determining the degree of sequence identity between two amino acid sequences, the skilled person may take into account so-called "conservative" amino acid substitutions, which can generally be described as amino acid substitutions in which an amino acid residue is replaced with another amino acid residue of similar chemical structure and which has little or essentially no influence on the function, activity or other biological properties of the polypeptide. Such conservative amino acid substitutions are well known in the art, for example from <patcit id="pcit0031" dnum="WO04037999A"><text>WO 04/037999</text></patcit>, <patcit id="pcit0032" dnum="GB2357768A"><text>GB-A-2 357 768</text></patcit>, <patcit id="pcit0033" dnum="WO9849185A"><text>WO 98/49185</text></patcit>, <patcit id="pcit0034" dnum="WO0046383A"><text>WO 00/46383</text></patcit> and <patcit id="pcit0035" dnum="WO0109300A"><text>WO 01/09300</text></patcit>; and (preferred) types and/or combinations of such substitutions may be selected on the basis of the pertinent teachings from <patcit id="pcit0036" dnum="WO04037999A"><text>WO 04/037999</text></patcit> as well as <patcit id="pcit0037" dnum="WO9849185A"><text>WO 98/49185</text></patcit> and from the further references cited therein.

0083Such conservative substitutions preferably are substitutions in which one amino acid within the following groups (a) - (e) is substituted by another amino acid residue within the same group: (a) small aliphatic, nonpolar or slightly polar residues: Ala, Ser, Thr, Pro and Gly; (b) polar, negatively charged residues and their (uncharged) amides: Asp, Asn, Glu and Gin; (c) polar, positively charged residues: His, Arg and Lys; (d) large aliphatic, nonpolar residues: Met, Leu, Ile, Val and Cys; and (e) aromatic residues: Phe, Tyr and Trp.

0084Particularly preferred conservative substitutions are as follows: Ala into Gly or into Ser; Arg into Lys; Asn into Gln or into His; Asp into Glu; Cys into Ser; Gln into Asn; Glu into Asp; Gly into Ala or into Pro; His into Asn or into Gln; Ile into Leu or into Val; Leu into Ile or into Val; Lys into Arg, into Gln or into Glu; Met into Leu, into Tyr or into Ile; Phe into Met, into Leu or into Tyr; Ser into Thr, Thr into Ser; Trp into Tyr; Tyr into Trp; and/or Phe into Val, into Ile or into Leu.

0085Any amino acid substitutions applied to the polypeptides described herein may also be based on the analysis of the frequencies of amino acid variations between homologous proteins of different species developed by <nplcit id="ncit0005" npl-type="b"><text>Schulz et al., Principles of Protein Structure, Springer-Verlag, 1978</text></nplcit>, on the analyses of structure forming potentials developed by <nplcit id="ncit0006" npl-type="s"><text>Chou and Fasman, Biochemistry 13: 211, 1974</text></nplcit> and <nplcit id="ncit0007" npl-type="s"><text>Adv. Enzymol., 47: 45-149, 1978</text></nplcit>, and on the analysis of hydrophobicity patterns in proteins developed by <nplcit id="ncit0008" npl-type="s"><text>Eisenberg et al., Proc. Nad. Acad Sci. USA 81: 140-144, 1984</text></nplcit>; <nplcit id="ncit0009" npl-type="s"><text>Kyte &amp; Doolittle; J Molec. Biol. 157: 105-132, 198 I</text></nplcit>, and <nplcit id="ncit0010" npl-type="s"><text>Goldman et al., Ann. Rev. Biophys. Chem. 15: 321-353, 1986</text></nplcit>, all incorporated herein in their entirety by reference. Information on the primary, secondary and tertiary structure of Nanobodies given in the description below and in the general background art cited above. Also, for this purpose, the crystal structure of a V_HH domain from a llama is for example given by <nplcit id="ncit0011" npl-type="s"><text>Desmyter et al., Nature Structural Biology, Vol. 3, 9, 803 (1996</text></nplcit>); <nplcit id="ncit0012" npl-type="s"><text>Spinelli et al., Natural Structural Biology (1996); 3, 752-757</text></nplcit>; and <nplcit id="ncit0013" npl-type="s"><text>Decanniere et al., Structure, Vol. 7,4, 361 (1999</text></nplcit>); <ul id="ul0021" list-style="none" compact="compact"><li>g) amino acid sequences and nucleic acid sequences are said to be <i>"exactly the same"</i> if they have 100% sequence identity (as defined herein) over their entire length;</li><li>h) when comparing two amino acid sequences, the term <i>"amino acid difference"</i> refers to an insertion, deletion or substitution of a single amino acid residue on a position of the first sequence, compared to the second sequence; it being understood that two amino acid sequences can contain one, two or more such amino acid differences;</li><li>i) a nucleic acid sequence or amino acid sequence is considered to be <i>"(in) essentially isolated (form)"</i> - for example, compared to its native biological source and/or the reaction medium or cultivation medium from which it has been obtained - when it has been separated from at least one other component with which it is usually associated in said source or medium, such as another nucleic acid, another protein/polypeptide, another biological component or macromolecule or at least one contaminant, impurity or minor component. In particular, a nucleic acid sequence or amino acid sequence is considered <i>"essentially isolated"</i> when it has been purified at least 2-fold, in particular at least 10-fold, more in particular at least 100-fold, and up to 1000-fold or more. A nucleic acid sequence or amino acid sequence that is "in essentially isolated form" is preferably essentially homogeneous, as determined using a suitable technique, such as a suitable chromatographical technique, such as polyacrylamide-gelelectrophoresis;</li><li>j) The term "domain" as used herein generally refers to a globular region of an antibody chain, and in particular to a globular region of a heavy chain antibody, or to a polypeptide that essentially consists of such a globular region. Usually, such a domain will comprise peptide loops (for example 3 or 4 peptide loops) stabilized, for example, as a sheet or by disulfide bonds.</li><li>k) The term 'antigenic determinant' refers to the epitope on the antigen recognized by the antigen-binding molecule (such as a Nanobody or a polypeptide of the invention) and more in particular by the antigen-binding site of said molecule. The terms "antigenic determinant" and "epitope' may also be used interchangeably herein.</li><li>l) An amino acid sequence (such as a Nanobody, an antibody, a polypeptide of the invention, or generally an antigen binding protein or polypeptide or a fragment thereof) that can bind to, that has affinity for and/or that has specificity for a specific antigenic determinant, epitope, antigen or protein (or for at least one part, fragment or epitope thereof) is said to be "against" or "directed against" said antigenic determinant, epitope, antigen or protein.</li><li>m) The term "specificity" refers to the number of different types of antigens or antigenic determinants to which a particular antigen-binding molecule or antigen-binding protein (such as a Nanobody or a polypeptide of the invention) molecule can bind. The specificity of an antigen-binding protein can be determined based on affinity and/or avidity. The affinity, represented by the equilibrium constant for the dissociation of an antigen with an antigen-binding protein (KD), is a measure for the binding strength between an antigenic determinant and an antigen-binding site on the antigen-binding protein: the lesser the value of the KD, the stronger the binding strength between an antigenic determinant and the antigen-binding molecule (alternatively, the affinity can also be expressed as the affinity constant (KA), which is 1/KD). As will be clear to the skilled person (for example on the basis of the further disclosure herein), affinity can be determined in a manner known per se, depending on the specific antigen of interest. Avidity is the measure of the strength of binding between an antigen-binding molecule (such as a Nanobody or polypeptide of the invention) and the pertinent antigen. Avidity is related to both the affinity between an antigenic determinant and its antigen binding site on the antigen-binding molecule and the number of pertinent binding sites present on the antigen-binding molecule. Typically, antigen-binding proteins (such as the Nanobodies and/or polypeptides of the invention) will bind with a dissociation constant (KD) of 10^-5 to 10^-12 moles/liter (M) or less, and preferably 10^-7 to 10^-12 moles/liter (M) or less and more preferably 10^-8 to 10^-12 moles/liter, and/or with an association constant(K_A) of at least 10⁷ M^-1 preferably at least 10⁸ M^-1, more preferably at least 10⁹ M-1, such as at least 10¹² M^-1. Any K_D value greater than 10^-4 M is generally considered to indicate nonspecific binding. Preferably, a Nanobody or polypeptide of the invention will bind to the desired antigen with an K_D less than 500 nM, preferably less than 200 nM, more preferably less than 10 nM, such as less than 500 pM. Specific binding of an antigen-binding protein to an antigen or antigenic determinant can be determined in any suitable manner known per se, including, for example, Scatchard analysis and/or competitive binding assays, such as radioimmunoassays (RIA), enzyme immunoassays (EIA) and sandwich competition assays, and the different variants thereof known per se in the art.</li><li>n) as further described hereinbelow, the amino acid sequence and structure of a Nanobody can be considered - without however being limited thereto - to be comprised of four framework regions or "FR's", which are referred to in the art and hereinbelow as <i>"Framework region 1</i>" or <i>"FR1";</i> as <i>"Framework region 2"</i> or <i>"FR2";</i> as <i>"Framework region 3"</i> or <i>"FR3";</i> and as <i>"Framework region 4</i>" or <i>"FR4",</i> respectively; which framework regions are interrupted by three complementary determining regions or "CDR's", which are referred to in the art as <i>"Complementarity Determining Region 1</i> "or <i>"CDR1";</i> as <i>"Complementarity Determining Region 2"</i> or <i>"CDR2";</i> and as <i>"Complementarity Determining Region 3</i>" or <i>"CDR3",</i> respectively;</li><li>o) as also further describe hereinbelow, the total number of amino acid residues in a Nanobody can be in the region of 110-120, is preferably 112-115, and is most preferably 113. It should however be noted that parts, fragments or analogs (as further described hereinbelow) of a Nanobody are not particularly limited as to their length and/or size, as long as such parts, fragments or analogs meet the further requirements outlined hereinbelow and are also preferably suitable for the purposes described herein;</li><li>p) the amino acid residues of a Nanobody are numbered according to the general numbering for V_H domains given by <nplcit id="ncit0014" npl-type="b"><text>Kabat et al. ("Sequence of proteins of immunological interest", US Public Health Services, NIH Bethesda, MD, Publication No. 91</text></nplcit>), as applied to V_HH domains from Camelids in the article of Riechmann and Muyldermans, referred to above (see for example <figref idref="f0001">Figure 2</figref> of said reference). According to this numbering, FR1 of a Nanobody comprises the amino acid residues at positions 1-30, CDR1 of a Nanobody comprises the amino acid residues at positions 31-36, FR2 of a Nanobody comprises the amino acids at positions 36-49, CDR2 of a Nanobody comprises the amino acid residues at positions 50-65, FR3 of a Nanobody comprises the amino acid residues at positions 66-94, CDR3 of a Nanobody comprises the amino acid residues at positions 95-102, and FR4 of a Nanobody comprises the amino acid residues at positions 103-113. [In this respect, it should be noted that - as is well known in the art for V_H domains and for V_HH domains - the total number of amino acid residues in each of the CDR's may vary and may not correspond to the total number of amino acid residues indicated by the Kabat numbering (that is, one or more positions according to the Kabat numbering may not be occupied in the actual sequence, or the actual sequence may contain more amino acid residues than the number allowed for by the Kabat numbering). This means that, generally, the numbering according to Kabat may or may not correspond to the actual numbering of the amino acid residues in the actual sequence. Generally, however, it can be said that, according to the numbering of Kabat and irrespective of the number of amino acid residues in the CDR's, position 1 according to the Kabat numbering corresponds to the start of FR1 and visa versa, position 36 according to the Kabat numbering corresponds to the start of FR2 and visa versa, position 66 according to the Kabat numbering corresponds to the start of FR3 and visa versa, and position 103 according to the Kabat numbering corresponds to the start of FR4 and visa versa.]. Alternative methods for numbering the amino acid residues of V_H domains, which methods can also be applied in an analogous manner to V_HH domains from Camelids and to Nanobodies, are the method described by <nplcit id="ncit0015" npl-type="s"><text>Chothia et al. (Nature 342, 877-883 (1989</text></nplcit>)), the so-called <i>"AbM definition"</i> and the so-called <i>"contact definition".</i> However, in the present description, claims and figures, the numbering according to Kabat as applied to V_HH domains by Riechmann and Muyldermans will be followed, unless indicated otherwise; and</li><li>q) the Figures, Sequence Listing and the Experimental Part/Examples are only given to further illustrate the invention and should not be interpreted or construed as limiting the scope of the invention and/or of the appended claims in any way, unless explicitly indicated otherwise herein.</li></ul>

0086For a general description of heavy chain antibodies and the variable domains thereof, reference is inter alia made to the following references, which are mentioned as general background art: <patcit id="pcit0038" dnum="WO9404678A"><text>WO 94/04678</text></patcit>, <patcit id="pcit0039" dnum="WO9504079A"><text>WO 95/04079</text></patcit> and <patcit id="pcit0040" dnum="WO9634103A"><text>WO 96/34103</text></patcit> of the Vrije Universiteit Brussel; <patcit id="pcit0041" dnum="WO9425591A"><text>WO 94/25591</text></patcit>, <patcit id="pcit0042" dnum="WO9937681A"><text>WO 99/37681</text></patcit>, <patcit id="pcit0043" dnum="WO0040968A"><text>WO 00/40968</text></patcit>, <patcit id="pcit0044" dnum="WO0043507A"><text>WO 00/43507</text></patcit>, <patcit id="pcit0045" dnum="WO0065057A"><text>WO 00/65057</text></patcit>, <patcit id="pcit0046" dnum="WO0140310A"><text>WO 01/40310</text></patcit>, <patcit id="pcit0047" dnum="WO0144301A"><text>WO 01/44301</text></patcit>, <patcit id="pcit0048" dnum="EP1134231A"><text>EP 1134231</text></patcit> and <patcit id="pcit0049" dnum="WO0248193A"><text>WO 02/48193</text></patcit> of Unilever; <patcit id="pcit0050" dnum="WO9749805A"><text>WO 97/49805</text></patcit>, <patcit id="pcit0051" dnum="WO0121817A"><text>WO 01/21817</text></patcit>, <patcit id="pcit0052" dnum="WO03035694A"><text>WO 03/035694</text></patcit>, <patcit id="pcit0053" dnum="WO03054016A"><text>WO 03/054016</text></patcit> and <patcit id="pcit0054" dnum="WO03055527A"><text>WO 03/055527</text></patcit> of the Vlaams Instituut voor Biotechnologie (VIB); <patcit id="pcit0055" dnum="WO03050531A"><text>WO 03/050531</text></patcit> of Algonomics N.V. and applicant; <patcit id="pcit0056" dnum="WO0190190A"><text>WO 01/90190</text></patcit> by the National Research Council of Canada; <patcit id="pcit0057" dnum="WO03025020A"><text>WO 03/025020</text></patcit> (= <patcit id="pcit0058" dnum="EP1433793A"><text>EP 1 433 793</text></patcit>) by the Institute of Antibodies; as well as <patcit id="pcit0059" dnum="WO04041867A"><text>WO 04/041867</text></patcit>, <patcit id="pcit0060" dnum="WO04041862A"><text>WO 04/041862</text></patcit>, <patcit id="pcit0061" dnum="WO04041865A"><text>WO 04/041865</text></patcit>, <patcit id="pcit0062" dnum="WO04041863A"><text>WO 04/041863</text></patcit>, <patcit id="pcit0063" dnum="WO04062551A"><text>WO 04/062551</text></patcit> by applicant and the further published patent applications by applicant; <nplcit id="ncit0016" npl-type="s"><text>Hamers-Casterman et al., Nature 1993 June 3; 363 (6428): 446-8</text></nplcit>; <nplcit id="ncit0017" npl-type="s"><text>Davies and Riechmann, FEBS Lett. 1994 Feb 21; 339(3): 285-90</text></nplcit>; <nplcit id="ncit0018" npl-type="s"><text>Muyldermans et al., Protein Eng. 1994 Sep; 7(9): 1129-3</text></nplcit>; <nplcit id="ncit0019" npl-type="s"><text>Davies and Riechmann, Biotechnology (NY) 1995 May; 13(5): 475-9</text></nplcit>; <nplcit id="ncit0020" npl-type="s"><text>Gharoudi et al., 9th Forum of Applied Biotechnology, Med. 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0087As mentioned above, the invention generally relates to Nanobodies directed against vWF, as well as to polypeptides comprising or essentially consisting of one or more of such Nanobodies, that can be used for the prophylactic, therapeutic and/or diagnostic purposes described below and in <patcit id="pcit0064" dnum="WO04062551A"><text>WO 04/062551</text></patcit>.

0088As also mentioned above and further described below, the invention further relates to nucleic acids encoding such Nanobodies and polypeptides, to methods for preparing such Nanobodies and polypeptides, to host cells expressing or capable of expressing such Nanobodies or polypeptides, to uses of such Nanobodies, polypeptides, nucleic acids or host cells, and to compositions comprising such Nanobodies, polypeptides, nucleic acids or host cells.

0089Generally, it should be noted that the term Nanobody as used herein in its broadest sense is not limited to a specific biological source or to a specific method of preparation. For example, as will be discussed in more detail below, the Nanobodies of the invention can be obtained (1) by isolating the V_HH domain of a naturally occurring heavy chain antibody; (2) by expression of a nucleotide sequence encoding a naturally occurring V_HH domain; (3) by "humanization" (as described below) of a naturally occurring V_HH domain or by expression of a nucleic acid encoding a such humanized V_HH domain; (4) by "camelization" (as described below) of a naturally occurring V_H domain from any animal species, in particular a species of mammal, such as from a human being, or by expression of a nucleic acid encoding such a camelized V_H domain; (5) by "camelisation" of a "domain antibody" or "Dab" as described by Ward et al (supra), or by expression of a nucleic acid encoding such a camelized V_H domain; (6) using synthetic or semi-synthetic techniques for preparing proteins, polypeptides or other amino acid sequences; (7) by preparing a nucleic acid encoding a Nanobody using techniques for nucleic acid synthesis, followed by expression of the nucleic acid thus obtained; and/or (8) by any combination of the foregoing. Suitable methods and techniques for performing the foregoing will be clear to the skilled person based on the disclosure herein and for example include the methods and techniques described in more detail hereinbelow.

0090However, according to a specific embodiment, the Nanobodies of the invention do not have an amino acid sequence that is exactly the same as (i.e. as a degree of sequence identity of 100% with) the amino acid sequence of a naturally occurring V_H domain, such as the amino acid sequence of a naturally occurring V_H domain from a mammal, and in particular from a human being.

0091One particularly preferred class of Nanobodies of the invention comprises Nanobodies with an amino acid sequence that corresponds to the amino acid sequence of a naturally occurring V_HH domain, but that has been "humanized" , i.e. by replacing one or more amino acid residues in the amino acid sequence of said naturally occurring V_HH sequence by one or more of the amino acid residues that occur at the corresponding positions) in a V_H domain from a conventional 4-chain antibody from a human being (e.g. indicated above). This can be performed in a manner known per se, which will be clear to the skilled person, for example on the basis of the further description below and the prior art on humanization referred to herein. Again, it should be noted that such humanized Nanobodies of the invention can be obtained in any suitable manner known per se (i.e. as indicated under points (1) - (8) above) and thus are not strictly limited to polypeptides that have been obtained using a polypeptide that comprises a naturally occurring V_HH domain as a starting material.

0092Another particularly preferred class of Nanobodies of the invention comprises Nanobodies with an amino acid sequence that corresponds to the amino acid sequence of a naturally occurring V_H domain that has been "camelized", i.e. by replacing one or more amino acid residues in the amino acid sequence of a naturally occurring V_H domain from a conventional 4-chain antibody by one or more of the amino acid residues that occur at the corresponding positions) in a V_HH domain of a heavy chain antibody. This can be performed in a manner known per se, which will be clear to the skilled person, for example on the basis of the further description below. Reference is also made to <patcit id="pcit0065" dnum="WO9404678A"><text>WO 94/04678</text></patcit>. Such camelization may preferentially occur at amino acid positions which are present at the V_H-V_L interface and at the so-called Camelidae hallmark residues (see for example also <patcit id="pcit0066" dnum="WO9404678A"><text>WO 94/04678</text></patcit>), as also mentioned below. Preferably, the V_H domain or sequence that is used as a starting material or starting point for generating or designing the camelized Nanobody is preferably a V_H sequence from a mammal, more preferably the V_H sequence of a human being. However, it should be noted that such camelized Nanobodies of the invention can be obtained in any suitable manner known per se (i.e. as indicated under points (1) - (8) above) and thus are not strictly limited to polypeptides that have been obtained using a polypeptide that comprises a naturally occurring V_H domain as a starting material.

0093For example, again as further described below, both "humanization" and "camelization" can be performed by providing a nucleotide sequence that encodes such a naturally occurring V_HH domain or V_H domain, respectively, and then changing, in a manner known per se, one or more codons in said nucleotide sequence such that the new nucleotide sequence encodes a humanized or camelized Nanobody of the invention, respectively, and then expressing the nucleotide sequence thus obtained in a manner known per se so as to provide the desired Nanobody of the invention. Alternatively, based on the amino acid sequence of a naturally occurring V_HH domain or V_H domain, respectively, the amino acid sequence of the desired humanized or camelized Nanobody of the invention, respectively, can be designed and then synthesized <i>de novo</i> using techniques for peptide synthesis known per se. Also, based on the amino acid sequence or nucleotide sequence of a naturally occurring V_HH domain or V_H domain, respectively, a nucleotide sequence encoding the desired humanized or camelized Nanobody of the invention, respectively, can be designed and then synthesized <i>de novo</i> using techniques for nucleic acid synthesis known per se, after which the nucleotide sequence thus obtained can be expressed in a manner known per se so as to provide the desired Nanobody of the invention.

0094Other suitable ways and techniques for obtaining Nanobodies of the invention and/or nucleotide sequences and/or nucleic acids encoding the same, starting from (the amino acid sequence of) naturally occurring V_H domains or preferably V_HH domains and/or from nucleotide sequences and/or nucleic acid sequences encoding the same will be clear from the skilled person, and may for example comprising combining one or more amino acid sequences and/or nucleotide sequences from naturally occurring V_H domains (such as one or more FR's and/or CDR's) with one or more one or more amino acid sequences and/or nucleotide sequences from naturally occurring V_HH domains (such an one or more FR's or CDR's), in a suitable manner so as to provide (a nucleotide sequence or nucleic acid encoding) a Nanobody of the invention.

0095According to one preferred, but non-limiting aspect of the aspect of the invention, a Nanobody in its broadest sense can be generally defined as a polypeptide comprising: <ol id="ol0017" compact="compact"><li>a) an amino acid sequence that is comprised of four framework regions/sequences interrupted by three complementarity determining regions/sequences, in which the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ol> and/or: <ul id="ul0022" list-style="none" compact="compact"><li>b) an amino acid sequence that is comprised of four framework regions/sequences interrupted by three complementarity determining regions/sequences, in which the amino acid residue at position 44 according to the Kabat numbering is E and in which the amino acid residue at position 45 according to the Kabat numbering is an R;</li></ul> and/or: <ul id="ul0023" list-style="none" compact="compact"><li>c) an amino acid sequence that is comprised of four framework regions/sequences interrupted by three complementarity determining regions/sequences, in which the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of P, R and S, and is in particular chosen from the group consisting of R and S.</li></ul>

0096Thus, in a first preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which <ol id="ol0018" compact="compact"><li>i) the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ol> and/or in which: <ul id="ul0024" list-style="none" compact="compact"><li>ii) the amino acid residue at position 44 according to the Kabat numbering is E and in which the amino acid residue at position 45 according to the Kabat numbering is an R;</li></ul> and/or in which: <ul id="ul0025" list-style="none" compact="compact"><li>iii) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of P, R and S, and is in particular chosen from the group consisting of R and S;</li></ul> and in which: iv) CDR 1 is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0009" num="0009"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>NYGMG</entry><entry>[SEQ ID NO: 15]</entry></row><row><entry>SYTLG</entry><entry>[SEQ ID NO: 16]</entry></row><row><entry>NYNMG</entry><entry>[SEQ ID NO: 17]</entry></row><row><entry>SSAMA</entry><entry>[SEQ ID NO: 18]</entry></row><row><entry>YYNTG</entry><entry>[SEQ ID NO: 19]</entry></row><row><entry>IGAMG</entry><entry>[SEQ ID NO: 20]</entry></row><row><entry>IGTMG</entry><entry>[SEQ ID NO: 21]</entry></row><row><entry>YNPMG</entry><entry>[SEQ ID NO: 22]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0019" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0020" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: v) CDR 2 is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0010" num="0010"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="44mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SISWSGTYTAYSDNVKG</entry><entry>[SEQ ID NO: 23]</entry></row><row><entry>GISWSGVSTDYAEFAKG</entry><entry>[SEQ ID NO: 24]</entry></row><row><entry>TSISWSGSYTAYADNVKG</entry><entry>[SEQ ID NO: 25]</entry></row><row><entry>SISWSGMSTYYTDSVKG</entry><entry>[SEQ ID NO: 26]</entry></row><row><entry>TITSGGRTSYADSVKG</entry><entry>[SEQ ID NO: 27]</entry></row><row><entry>AISWSGGLTYYADSVKG</entry><entry>[SEQ ID NO: 28]</entry></row><row><entry>TITSGGSTNYADPVKG</entry><entry>[SEQ ID NO: 29]</entry></row><row><entry>TITSGGSTNYADSVKG</entry><entry>[SEQ ID NO: 30]</entry></row><row><entry>AISRTGGSTYYARSVEG</entry><entry>[SEQ ID NO: 31]</entry></row><row><entry>AISRTGGSTYYPDSVEG</entry><entry>[SEQ ID NO: 32]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0021"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0022"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: vi) CDR 3 is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0011" num="0011"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>QSRYRSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 33]</entry></row><row><entry>LGRYRSNWRNIGQYDY</entry><entry>[SEQ ID NO: 34]</entry></row><row><entry>QSRYSSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 35]</entry></row><row><entry>SNRYRTHTTQAMYNY</entry><entry>[SEQ ID NO: 36]</entry></row><row><entry>VVDGKRAP</entry><entry>[SEQ ID NO: 37]</entry></row><row><entry>NRRQKTVQMGERAYDY</entry><entry>[SEQ ID NO: 38]</entry></row><row><entry>NLKQGSYGYRFNDY</entry><entry>[SEQ ID NO: 39]</entry></row><row><entry>NLKQGDYGYRFNDY</entry><entry>[SEQ ID NO: 40]</entry></row><row><entry>AGVRAEDGRVRTLPSEYNF</entry><entry>[SEQ ID NO: 41]</entry></row><row><entry>AGVRAEDGRVRTLPSEYTF</entry><entry>[SEQ ID NO: 42]</entry></row><row><entry>AGVRAEDGRVRSLPSEYTF</entry><entry>[SEQ ID NO: 43]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0023" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0024" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol>

0097Preferably, in the Nanobodies of the invention: <ul id="ul0026" list-style="dash" compact="compact"><li>when CDR1 is chosen from the group consisting of (1) NYGMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) SISWSGTYTAYSDNVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) QSRYRSNYYDHDDKYAY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) SYTLG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) GISWSGVSTDYAEFAKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) LGRYRSNWRNIGQYDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) NYGMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TSISWSGSYTAYADNVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) QSRYSSNYYDHDDKYAY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) NYNMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) SISWSGMSTYYTDSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) SNRYRTHTTQAMYNY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) SSAMA; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TITSGGRTSYADSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) WDGKRAP; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) YYNTG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) AISWSGGLTYYADSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) NRRQKTVQMGERAYDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) IGAMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TITSGGSTNYADPVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) NLKQGSYGYRFNDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) IGAMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TITSGGSTNYADSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) NLKQGSYGYRFNDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) IGAMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TITSGGSTNYADSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) NLKQGDYGYRFNDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) IGTMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) TITSGGSTNYADSVKG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) NLKQGDYGYRFNDY; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) YNPMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) AISRTGGSTYYARSVEG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) AGVRAEDGRVRTLPSEYNF; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) YNPMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) AISRTGGSTYYPDSVEG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) AGVRAEDGRVRTLPSEYTF; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence;</li><li>when CDR1 is chosen from the group consisting of (1) YNPMG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; then CDR2 is chosen from the group consisting of (1) AISRTGGSTYYPDSVEG; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; and CDR3 is chosen from the group consisting of (1) AGVRAEDGRVRSLPSEYTF; (2) amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with said amino acid sequence; and (3) amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with said amino acid sequence; in which <ol id="ol0025" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol></li></ul>

0098In particular, a Nanobody against vWF according to the invention may have the structure: FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which <ol id="ol0026" compact="compact"><li>i) the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ol> and/or in which: <ul id="ul0027" list-style="none" compact="compact"><li>ii) the amino acid residue at position 44 according to the Kabat numbering is E and in which the amino acid residue at position 45 according to the Kabat numbering is an R;</li></ul> and/or in which: <ul id="ul0028" list-style="none" compact="compact"><li>iii) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of P, R and S, and is in particular chosen from the group consisting of R and S;</li></ul> and in which: iv) CDR I is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0012" num="0012"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>NYGMG</entry><entry>[SEQ ID NO: 15]</entry></row><row><entry>SYTLG</entry><entry>[SEQ ID NO: 16]</entry></row><row><entry>NYNMG</entry><entry>[SEQ ID NO: 17]</entry></row><row><entry>SSAMA</entry><entry>[SEQ ID NO: 18]</entry></row><row><entry>YYNTG</entry><entry>[SEQ ID NO: 19]</entry></row><row><entry>IGAMG</entry><entry>[SEQ ID NO: 20]</entry></row><row><entry>IGTMG</entry><entry>[SEQ ID NO: 21]</entry></row><row><entry>YNPMG</entry><entry>[SEQ ID NO: 22]</entry></row></tbody></tgroup></table></tables> and in which: v) CDR 2 is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0013" num="0013"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="44mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SISWSGTYTAYSDNVKG</entry><entry>[SEQ ID NO: 23]</entry></row><row><entry>GISWSGVSTDYAEFAKG</entry><entry>[SEQ ID NO: 24]</entry></row><row><entry>TSISWSGSYTAYADNVKG</entry><entry>[SEQ ID NO: 25]</entry></row><row><entry>SISWSGMSTYYTDSVKG</entry><entry>[SEQ ID NO: 26]</entry></row><row><entry>TITSGGRTSYADSVKG</entry><entry>[SEQ ID NO: 27]</entry></row><row><entry>AISWSGGLTYYADSVKG</entry><entry>[SEQ ID NO: 28]</entry></row><row><entry>TITSGGSTNYADPVKG</entry><entry>[SEQ ID NO: 29]</entry></row><row><entry>TITSGGSTNYADSVKG</entry><entry>[SEQ ID NO: 30]</entry></row><row><entry>AISRTGGSTYYARSVEG</entry><entry>[SEQ ID NO: 31]</entry></row><row><entry>AISRTGGSTYYPDSVEG</entry><entry>[SEQ ID NO: 32]</entry></row></tbody></tgroup></table></tables> and in which: vi) CDR 3 is an amino acid sequence that is chosen from the group consisting of the following amino acid sequences: <tables id="tabl0014" num="0014"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>QSRYRSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 33]</entry></row><row><entry>LGRYRSNWRNIGQYDY</entry><entry>[SEQ ID NO: 34]</entry></row><row><entry>QSRYSSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 35]</entry></row><row><entry>SNRYRTHTTQAMYNY</entry><entry>[SEQ ID NO: 36]</entry></row><row><entry>WDGKRAP</entry><entry>[SEQ ID NO: 37]</entry></row><row><entry>NRRQKTVQMGERAYDY</entry><entry>[SEQ ID NO: 38]</entry></row><row><entry>NLKQGSYGYRFNDY</entry><entry>[SEQ ID NO: 39]</entry></row><row><entry>NLKQGDYGYRFNDY</entry><entry>[SEQ ID NO: 40]</entry></row><row><entry>AGVRAEDGRVRTLPSEYNF</entry><entry>[SEQ ID NO: 41]</entry></row><row><entry>AGVRAEDGRVRTLPSEYTF</entry><entry>[SEQ ID NO: 42]</entry></row><row><entry>AGVRAEDGRVRSLPSEYTF</entry><entry>[SEQ ID NO: 43]</entry></row></tbody></tgroup></table></tables>

0099Preferably, in the Nanobodies of the invention according to the latter aspect: <ul id="ul0029" list-style="dash"><li>When CDR1 is:NYGMG; then CDR2 is:SISWSGTYTAYSDNVKG; and CDR3 is:QSRYRSNYYDHDDKYAY</li><li>When CDR1 is:SYTLG; then CDR2 is:GISWSGVSTDYAEFAKG; and CDR3 is:LGRYRSNWRNIGQYDY</li><li>When CDR1 is:NYGMG; then CDR2 is:TSISWSGSYTAYADNVKG; and CDR3 is:QSRYSSNYYDHDDKYAY</li><li>When CDR1 is:NYNMG; then CDR2 is:SISWSGMSTYYTDSVKG; and CDR3 is:SNRYRTHTTQAMYNY</li><li>When CDR1 is:SSAMA; then CDR2 is:TITSGGRTSYADSVKG; and CDR3 is:VVDGKRAP</li><li>When CDR1 is:YYNTG; then CDR2 is:AISWSGGLTYYADSVKG; and CDR3 is:NRRQKTVQMGERAYDY</li><li>When CDR1 is:IGAMG; then CDR2 is:TITSGGSTNYADPVKG; and CDR3 is:NLKQGSYGYRFNDY</li><li>When CDR1 is:IGAMG; then CDR2 is:TITSGGSTNYADSVKG; and CDR3 is:NLKQGSYGYRFNDY</li><li>When CDR1 is:IGAMG; then CDR2 is:TITSGGSTNYADSVKG; and CDR3 is:NLKQGDYGYRFNDY</li><li>When CDR1 is:IGTMG; then CDR2 is: TITSGGSTNYADSVKG; and CDR3 is:NLKQGDYGYRFNDY</li><li>When CDR1 is:YNPMG; then CDR2 is:AISRTGGSTYYARSVEG; and CDR3 is:AGVRAEDGR VRTLPSEYNF</li><li>When CDR1 is:YNPMG;CDR2:AISRTGGSTYYPDSVEG; and CDR3 is:AGVRAEDGRVRTLPSEYTF</li><li>When CDR1 is:YNPMG; then CDR2 is:AISRTGGSTYYPDSVEG; and CDR3 is:AGVRAEDGRVRSLPSEYTF</li></ul>

0100In particular, according to one preferred, but non-limiting aspect of the aspect of the invention, a Nanobody can generally be defined as a polypeptide comprising an amino acid sequence that is comprised of four framework regions/sequences interrupted by three complementarity determining regions/sequences, in which; <ul id="ul0030" list-style="none" compact="compact"><li>a-1) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of G, E, D, G, Q, R, S, L; and is preferably chosen from the group consisting of G, E or Q; and</li><li>a-2) the amino acid residue at position 45 according to the Kabat numbering is chosen from the group consisting of L, R or C; and is preferably chosen from the group consisting of L or R; and</li><li>a-3) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of W, R or S; and is preferably W or R, and is most preferably W;</li><li>a-4) the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ul> or in which: <ul id="ul0031" list-style="none" compact="compact"><li>b-1) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of E and Q; and</li><li>b-2) the amino acid residue at position 45 according to the Kabat numbering is R; and</li><li>b-3) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of W, R and S; and is preferably W;</li><li>b-4) the amino acid residue at position 108 according to the Kabat numbering is chosen from the group consisting of Q and L; and is preferably Q;</li></ul> or in which: <ul id="ul0032" list-style="none" compact="compact"><li>c-1) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of G, E, D, Q, R, S and L; and is preferably chosen from the group consisting of G, E and Q; and</li><li>c-2) the amino acid residue at position 45 according to the Kabat numbering is chosen from the group consisting of L, R and C; and is preferably chosen from the group consisting of L and R; and</li><li>c-3) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of P, R and S; and is in particular chosen from the group consisting of R and S; and</li><li>c-4) the amino acid residue at position 108 according to the Kabat numbering is chosen from the group consisting of Q and L; is preferably Q.</li></ul>

0101Thus, in another preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0027" compact="compact"><li>i) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of G, E, D, G, Q, R, S, L; and is preferably chosen from the group consisting of G, E or Q;</li></ol> and in which: <ul id="ul0033" list-style="none" compact="compact"><li>ii) the amino acid residue at position 45 according to the Kabat numbering is chosen from the group consisting of L, R or C; and is preferably chosen from the group consisting of L or R;</li></ul> and in which: <ul id="ul0034" list-style="none" compact="compact"><li>iii) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of W, R or S; and is preferably W or R, and is most preferably W; and in which</li><li>iv) the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ul> and in which: <ul id="ul0035" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0102In another preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0028" compact="compact"><li>i) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of E and Q;</li></ol> and in which: <ul id="ul0036" list-style="none" compact="compact"><li>ii) the amino acid residue at position 45 according to the Kabat numbering is R;</li></ul> and in which: <ul id="ul0037" list-style="none" compact="compact"><li>iii) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of W, R and S; and is preferably W;</li></ul> and in which: <ul id="ul0038" list-style="none" compact="compact"><li>iv) the amino acid residue at position 108 according to the Kabat numbering is Q;</li></ul> and in which: <ul id="ul0039" list-style="none" compact="compact"><li>vi) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0103In another preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0029" compact="compact"><li>i) the amino acid residue at position 44 according to the Kabat numbering is chosen from the group consisting of G, E, D, Q, R, S and L; and is preferably chosen from the group consisting of G, E and Q;</li></ol> and in which: <ul id="ul0040" list-style="none" compact="compact"><li>ii) the amino acid residue at position 45 according to the Kabat numbering is chosen from the group consisting of L, R and C; and is preferably chosen from the group consisting of L and R;</li></ul> and in which: <ul id="ul0041" list-style="none" compact="compact"><li>iii) the amino acid residue at position 103 according to the Kabat numbering is chosen from the group consisting of P, R and S; and is in particular chosen from the group consisting of R and S;</li></ul> and in which: <ul id="ul0042" list-style="none" compact="compact"><li>iv) the amino acid residue at position 108 according to the Kabat numbering is chosen from the group consisting of Q and L; is preferably Q;</li></ul> and in which: <ul id="ul0043" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0104Two particularly preferred, but non-limiting groups of the Nanobodies of the invention are those according to a) above; according to a-1) to a-4) above; according to b) above; according to b-1) to b-4) above; according to c) above; and/or according to c-1) to c-4) above, in which; <ol id="ol0030" compact="compact"><li>a) the amino acid residues at positions 44-47 according to the Kabat numbering form the sequence GLEW (or a GLEW-like sequence as defined herein) and the amino acid residue at position 108 is Q;</li></ol> or in which: <ul id="ul0044" list-style="none" compact="compact"><li>b) the amino acid residues at positions 43-46 according to the Kabat numbering form the sequence KERE or KQRE (or a KERE-like sequence) and the amino acid residue at position 108 is Q or L, and is preferably Q.</li></ul>

0105Thus, in another preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0031" compact="compact"><li>i) the amino acid residues at positions 44-47 according to the Kabat numbering form the sequence GLEW (or a GLEW-like sequence as defined herein) and the amino acid residue at position 108 is Q;</li></ol> and in which: <ul id="ul0045" list-style="none" compact="compact"><li>ii) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0106In another preferred, but non-limiting aspect, a Nanobody of the invention may have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0032" compact="compact"><li>i) the amino acid residues at positions 43-46 according to the Kabat numbering form the sequence KERE or KQRE (or a KERE-like sequence) and the amino acid residue at position 108 is Q or L, and is preferably Q;</li></ol> and in which: <ul id="ul0046" list-style="none" compact="compact"><li>ii) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0107In the Nanobodies of the invention in which the amino acid residues at positions 43-46 according to the Kabat numbering form the sequence KERE or KQRE, the amino acid residue at position 37 is most preferably F. In the Nanobodies of the invention in which the amino acid residues at positions 44-47 according to the Kabat numbering form the sequence GLEW, the amino acid residue at position 37 is chosen from the group consisting of Y, H, I, V or F, and is most preferably F.

0108Thus, without being limited hereto in any way, on the basis of the amino acid residues present on the positions mentioned above, the Nanobodies of the invention can generally be classified is on the basis of the following three groups: <ol id="ol0033" compact="compact"><li>a) The <i>"GLEW-group":</i> Nanobodies with the amino acid sequence GLEW at positions 44-47 according to the Kabat numbering and Q at position 108 according to the Kabat numbering. As further described herein, Nanobodies within this group usually have a V at position 37, and can have a W, P, R or S at position 103, and preferably have a W at position 103. The GLEW group also comprises some GLEW-like sequences such as those mentioned in Table 2 below;</li><li>b) The <i>"KERB-group":</i> Nanobodies with the amino acid sequence KERE or KQRE or at positions 43-46 according to the Kabat numbering and Q or L at position 108 according to the Kabat numbering. As further described herein, Nanobodies within this group usually have a F at position 37, an L or F at position 47; and can have a W, P, R or S at position 103, and preferably have a W at position 103;</li><li>c) The <i>"103 P, R, S-group":</i> Nanobodies with a P R or S at position 103. These Nanobodies can have either the amino acid sequence GLEW at positions 44-47 of the Kabat numbering or the amino acid sequence KERE or KQRE at positions 43-46 according to the Kabat numbering, the latter most preferably in combination with an F at position 37 and an L or an F at position 47 (as defined for the KERE-group); and can have Q or L at position 108 according to the Kabat numbering, and preferably have Q.</li></ol>

0109Thus, in another preferred, but non-limiting aspect, a Nanobody of the invention may be a Nanobody belonging to the GLEW-group (as defined herein), and in which CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.

0110In another preferred, but non-limiting aspect, a Nanobody of the invention may be a Nanobody belonging to the KERE-group (as defined herein), and in which CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.

0111Thus, in another preferred, but non-limiting aspect, a Nanobody of the invention may be a Nanobody belonging to the 103 P, R, S-group (as defined herein), and in which CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.

0112Also, more generally and in addition to the 108Q, 43E/44R and 103P,R,S residues mentioned above, the Nanobodies of the invention can contain, at one or more positions that, in a conventional V_H domain, would form (part of) the V_H/V_L interface, contain one or more amino acid residues that are more highly charged than the amino acid residues that naturally occur at the same position(s) in the corresponding naturally occurring V_H or V_HH domain, and in particular one or more charged amino acid residues (as mentioned in Table 1).

0113Such substitutions include, but are not limited to the GLEW-like sequences mentioned in Table 2 below; as well as the substitutions that are described in the International Application <patcit id="pcit0067" dnum="WO0029004A"><text>WO 00/29004</text></patcit> for so-called <i>"microbodies",</i> e.g. a Q at position 108 and KLEW at positions 44-47.

0114In the Nanobodies of the invention, the amino acid residue at position 83 is chosen from the group consisting of L, M, S, V and W; and is preferably L.

0115Also, in the Nanobodies of the invention, the amino acid residue at position 83 is chosen from the group consisting of R, K, N, E, I and Q; and is most preferably either K or E (for Nanobodies corresponding to naturally occurring V_HH domains) or R (for "humanized" Nanobodies, as described below). The amino acid residue at position 84 is chosen from the group consisting of P, A, R, S, D and V, and is most preferably P (for Nanobodies corresponding to naturally occurring V_HH domains) or R (for "humanized" Nanobodies, as described below).

0116Furthermore, in the Nanobodies of the invention, the amino acid residue at position 104 is chosen from the group consisting of G and D; and is most preferably G.

0117Collectively, the amino acid residues at positions 11, 37, 44, 45, 47, 83, 84, 103, 104 and 108, which in the Nanobodies are as mentioned above, will also be referred to herein as the <i>"Hallmark Residues".</i> The Hallmark Residues and the amino acid residues at the corresponding positions of the most closely related human VH domain, VH3, are summarized in Table 2.

0118Some especially preferred combinations of these Hallmark Residues as occur in naturally occurring V_HH domains are mentioned in Table 3. For comparison, the corresponding amino acid residues of the human V_H3 called DP-47 have been indicated in italics. <tables id="tabl0015" num="0015"><table frame="all"><title><b>Table 2: Hallmark Residues in Nanobodies</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="18mm" /><colspec colnum="2" colname="col2" colwidth="42mm" /><colspec colnum="3" colname="col3" colwidth="107mm" /><thead><row><entry valign="top">Position</entry><entry valign="top">Human V_H3</entry><entry valign="top">Hallmark Residues</entry></row></thead><tbody><row><entry>11</entry><entry>L, V; predominantly L</entry><entry>L, M, S, V,W; preferably L</entry></row><row><entry>37</entry><entry>V, I, F; usually V</entry><entry>F⁽¹⁾, Y, H, I or V, preferably F⁽¹⁾ or Y</entry></row><row><entry>44⁽⁸⁾</entry><entry>G</entry><entry>G⁽²⁾, E⁽³⁾, D, Q, R, S, L; preferably G⁽²⁾, E⁽³⁾ or Q; most preferably G⁽²⁾ or E⁽³⁾.</entry></row><row><entry>45⁽⁸⁾</entry><entry>L</entry><entry>L⁽²⁾, R⁽³⁾, C, I, L, P, Q, V; preferably L⁽²⁾ or R⁽³⁾</entry></row><row><entry>47⁽⁸⁾</entry><entry>W, Y</entry><entry>W⁽²⁾, L⁽¹⁾ or F⁽¹⁾, A, G, I, M, R, S or Y; preferably W⁽²⁾, L⁽¹⁾, F⁽¹⁾ or R</entry></row><row><entry>83</entry><entry>R or K; usually R</entry><entry>R, K⁽⁵⁾, N, E⁽⁵⁾, I, M or Q; preferably K or R; most preferably K</entry></row><row><entry>84</entry><entry>A, T, D; predominantly A</entry><entry>P⁽⁵⁾, A, L, R, S, D, V; preferably P</entry></row><row><entry>103</entry><entry>W</entry><entry>W⁽⁴⁾, P⁽⁶⁾, R⁽⁶⁾, S; preferably W</entry></row><row><entry>104</entry><entry>G</entry><entry>G or D; preferably G</entry></row><row><entry>108</entry><entry>L, M or T; predominantly L</entry><entry>Q, L⁽⁷⁾ or R; preferably Q or L⁽⁷⁾</entry></row></tbody></tgroup><tgroup cols="3" rowsep="0"><colspec colnum="1" colname="col1" colwidth="18mm" /><colspec colnum="2" colname="col2" colwidth="42mm" /><colspec colnum="3" colname="col3" colwidth="107mm" /><tbody><row><entry namest="col1" nameend="col3" align="justify"><u>Notes:</u> (1): In particular, but not exclusively, in combination with KERE or KQRE at positions 43-46. (2): Usually as GLEW at positions 44-47. (3): Usually as KERE or KQRE at positions 43-46, e.g. as KEREL, KEREF, KQREL, KQREF or KEREG at positions 43-47. Alternatively, also sequences such as TERE (for example TEREL), KECE (for example KECEL or KECER), RERE (for example REREG), QERE (for example QEREG), KGRE (for example KGREG), KDRE (for example KDREV) are possible. Some other possible, but less preferred sequences include for example DECKL and NVCEL. (4): With both GLEW at positions 44-47 and KERE or KQRE at positions 43-46. (5): Often as KP or EP at positions 83-84 of naturally occurring V_HH domains. (6): In particular, but not exclusively, in combination with GLEW at positions 44-47. (7): With the proviso that when positions 44-47 are GLEW, position 108 is always Q. (8): The GLEW group also contains GLEW-like sequences at positions 44-47, such as for example GVEW, EPEW, GLER, DQEW, DLEW, GIEW, ELEW, GPEW, EWLP, GPER, GLER and ELEW.</entry></row></tbody></tgroup></table></tables><tables id="tabl0016" num="0016"><table frame="all"><title><b>Table 3: Some preferred combinations of Hallmark Residues in naturally occurring Nanobodies.</b> For humanization of these combinations, reference is made to the specification.</title><tgroup cols="11"><colspec colnum="1" colname="col1" colwidth="22mm" /><colspec colnum="2" colname="col2" colwidth="15mm" /><colspec colnum="3" colname="col3" colwidth="15mm" /><colspec colnum="4" colname="col4" colwidth="15mm" /><colspec colnum="5" colname="col5" colwidth="15mm" /><colspec colnum="6" colname="col6" colwidth="15mm" /><colspec colnum="7" colname="col7" colwidth="15mm" /><colspec colnum="8" colname="col8" colwidth="15mm" /><colspec colnum="9" colname="col9" colwidth="15mm" /><colspec colnum="10" colname="col10" colwidth="15mm" /><colspec colnum="11" colname="col11" colwidth="15mm" /><thead><row><entry valign="top" /><entry valign="top"><b>11</b></entry><entry valign="top"><b>37</b></entry><entry valign="top"><b>44</b></entry><entry valign="top"><b>45</b></entry><entry valign="top"><b>47</b></entry><entry valign="top"><b>83</b></entry><entry valign="top"><b>84</b></entry><entry valign="top"><b>103</b></entry><entry valign="top"><b>104</b></entry><entry valign="top"><b>108</b></entry></row></thead><tbody><row><entry><i>DP-47 (human)</i></entry><entry><i>M</i></entry><entry><i>V</i></entry><entry><i>G</i></entry><entry><i>L</i></entry><entry><i>W</i></entry><entry><i>R</i></entry><entry><i>A</i></entry><entry><i>W</i></entry><entry><i>G</i></entry><entry><i>L</i></entry></row><row><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /></row><row><entry>"KERE" group</entry><entry>L</entry><entry>F</entry><entry>E</entry><entry>R</entry><entry>L</entry><entry>K</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>F</entry><entry>E</entry><entry>R</entry><entry>F</entry><entry>E</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>F</entry><entry>E</entry><entry>R</entry><entry>F</entry><entry>K</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>Y</entry><entry>Q</entry><entry>R</entry><entry>L</entry><entry>K</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>F</entry><entry>L</entry><entry>R</entry><entry>V</entry><entry>K</entry><entry>P</entry><entry>Q</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>F</entry><entry>Q</entry><entry>R</entry><entry>L</entry><entry>K</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>L</entry><entry>F</entry><entry>E</entry><entry>R</entry><entry>F</entry><entry>K</entry><entry>P</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /><entry /></row><row><entry>"GLEW" group</entry><entry>L</entry><entry>V</entry><entry>G</entry><entry>L</entry><entry>W</entry><entry>K</entry><entry>S</entry><entry>W</entry><entry>G</entry><entry>Q</entry></row><row><entry /><entry>M</entry><entry>V</entry><entry>G</entry><entry>L</entry><entry>W</entry><entry>K</entry><entry>P</entry><entry>R</entry><entry>G</entry><entry>Q</entry></row></tbody></tgroup></table></tables>

0119In the Nanobodies, each amino acid residue at any other position than the Hallmark Residues can be any amino acid residue that naturally occurs at the corresponding position (according to the Kabat numbering) of a naturally occurring V_HH domain.

0120Such amino acid residues will be clear to the skilled person. Tables 4 - 7 mention some non-limiting residues that can be present at each position (according to the Kabat numbering) of the FR1, FR2, FR3 and FR4 of naturally occurring V_HH domains. For each position, the amino acid residue that most frequently occurs at each position of a naturally occurring V_HH domain (and which is the most preferred amino acid residue for said position in a Nanobody) is indicated in bold; and other preferred amino acid residues for each position have been underlined (note: the number of amino acid residues that are found at positions 26-30 of naturally occurring V_HH domains supports the hypothesis underlying the numbering Chothia (supra) that the residues at these positions already form part of CDR1.)

0121In Tables 4 - 7, some of the non-limiting residues that can be present at each position of a human V_H3 domain have also been mentioned. Again, for each position, the amino acid residue that most frequently occurs at each position of a naturally occurring human V_H3 domain is indicated in bold; and other preferred amino acid residues have been underlined. <tables id="tabl0017" num="0017"><table frame="all"><title><b>Table 4: Non-limiting examples of amino acid residues in FR1 (for the footnotes, see the footnotes to Table 2)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="51mm" /><colspec colnum="2" colname="col2" colwidth="54mm" /><colspec colnum="3" colname="col3" colwidth="61mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>1</entry><entry><b>E</b>, <u>Q</u></entry><entry><b>Q</b>, A, E, D, H, R</entry></row><row><entry>2</entry><entry><b>V</b></entry><entry><b>V</b>, A, E, G, L, M, Q</entry></row><row><entry>3</entry><entry><b>Q</b></entry><entry><b>Q</b>, K, E, H, P, R, Y</entry></row><row><entry>4</entry><entry><b>L</b></entry><entry><b>L</b>, F, P, R, V</entry></row><row><entry>5</entry><entry><b>V</b>, L</entry><entry><b>Q</b>, E, L, V, M, P, A, I</entry></row><row><entry>6</entry><entry><b>E</b></entry><entry><b>E</b>, D, Q, A, H</entry></row><row><entry>7</entry><entry><b>S</b>, T</entry><entry><b>S</b>, F, H</entry></row><row><entry>8</entry><entry><b>G</b>, R</entry><entry><b>G</b>, A, R</entry></row><row><entry>9</entry><entry><b>G</b></entry><entry><b>G</b>, E</entry></row><row><entry>10</entry><entry><b>G</b>, V</entry><entry><b>G</b>, D, R, A, E, N, T, V</entry></row><row><entry>11</entry><entry namest="col2" nameend="col3" align="left"><b>Hallmark residue:</b> L, M, S, V,W, F, N, P, T, Y; preferably L</entry></row><row><entry>12</entry><entry><b>V</b>, I</entry><entry><b>V</b>, A, G, M</entry></row><row><entry>13</entry><entry><b>Q</b>, K, R</entry><entry><b>Q</b>, E, K, D, G, A, H, L, N, P, R, T</entry></row><row><entry>14</entry><entry><b>P</b></entry><entry><b>A</b>, <u>Q</u>, A, G, P, T, V, E, F, I, N, S</entry></row><row><entry>15</entry><entry><b>G</b></entry><entry><b>G</b></entry></row><row><entry>16</entry><entry><b>G</b>, <u>R</u></entry><entry><b>G</b>, A, E, D, N, P, R, S, V, W</entry></row><row><entry>17</entry><entry><b>S</b></entry><entry><b>S</b>, <u>F,</u> T, N, P, A, C</entry></row><row><entry>18</entry><entry><b>L</b></entry><entry><b>L</b>, V, M, Q, R</entry></row><row><entry>19</entry><entry><b>R</b>, K</entry><entry><b>R</b>, K, L, N, S, T, A, F, G, I, M, Q</entry></row><row><entry>20</entry><entry><b>L</b></entry><entry><b>L</b>, <u>F,</u> I, V, M, S</entry></row><row><entry>21</entry><entry><b>S</b></entry><entry><b>S</b>, F, T, G, H, P, A</entry></row><row><entry>22</entry><entry><b>C</b></entry><entry><b>C</b></entry></row><row><entry>23</entry><entry><b>A</b>, T</entry><entry><b>A</b>, D, P, S, T, V, E, G, I, L, Q, R</entry></row><row><entry>24</entry><entry><b>A</b></entry><entry><b>A</b>, I, S, T, V, C, E, F, G, L, N, P, Q, Y</entry></row></tbody></tgroup></table></tables><tables id="tabl0018" num="0018"><table frame="all"><title><b>Table 4: Non-limiting examples of amino acid residues in FR1 (continued)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="35mm" /><colspec colnum="2" colname="col2" colwidth="38mm" /><colspec colnum="3" colname="col3" colwidth="65mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>25</entry><entry><b>S</b></entry><entry><b>S</b>, A, F, P, T, L, V</entry></row><row><entry>26</entry><entry><b>G</b></entry><entry><b>G</b>, D, E, R, S, V, A, 1, M, P, T</entry></row><row><entry>27</entry><entry><b>F</b></entry><entry>S, F, R, L, P, G, N, A, D, E, H, I, K, M, Q, T, V, Y</entry></row><row><entry>28</entry><entry><b>T</b></entry><entry>N, T, E, D, S, I, R, A, G, R, F, Y, L, M, P, V</entry></row><row><entry>29</entry><entry><b>F</b>, <u>V</u></entry><entry>F, L, D, S, I, G, V, A, E, P, T, Y</entry></row><row><entry>30</entry><entry><b>S</b>, <u>D</u>, G</entry><entry>N, S, E, G, A, D, M, T, H, I, P, R, V, W</entry></row></tbody></tgroup></table></tables><tables id="tabl0019" num="0019"><table frame="all"><title><b>Table 5: Non-limiting examples of amino acid residues in FR2 (for the footnotes, see the footnotes to Table 2)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="38mm" /><colspec colnum="2" colname="col2" colwidth="63mm" /><colspec colnum="3" colname="col3" colwidth="65mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>36</entry><entry><b>W</b></entry><entry><b>W</b></entry></row><row><entry>37</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue</u>:</b> F⁽¹⁾, Y, H, I, A, L, P, S or V preferably F⁽¹⁾ or Y</entry></row><row><entry>38</entry><entry><b>R</b></entry><entry><b>R</b></entry></row><row><entry>39</entry><entry><b>Q</b></entry><entry><b>Q</b>, H, P, R, A, D, G, L, E</entry></row><row><entry>40</entry><entry><b>A</b></entry><entry><b>A</b>, F, G, P, T, V, I, L, N, R, S, Y</entry></row><row><entry>41</entry><entry><b>P</b>, S, T</entry><entry><b>P</b>, A, L, S, I, Q, T</entry></row><row><entry>42</entry><entry><b>G</b></entry><entry><b>G</b>, E, D, R, T, V</entry></row><row><entry>43</entry><entry><b>K</b></entry><entry><b>K</b>, D, E, N, Q, R, T, V, A, L, M, S</entry></row><row><entry rowsep="0">44</entry><entry namest="col2" nameend="col3" rowsep="0" align="left"><b><u>Hallmark residue:</u></b> G⁽²⁾, E⁽³⁾, D, Q, R, S, L, A, F, K, M, N, P, V, W, Y;</entry></row><row><entry rowsep="0" /><entry namest="col2" nameend="col3" rowsep="0" align="left">preferably G⁽²⁾, E⁽³⁾ or Q;</entry></row><row><entry /><entry namest="col2" nameend="col3" align="left">most preferably G⁽²⁾ or E⁽³⁾.</entry></row><row><entry>45</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> L⁽²⁾, R⁽³⁾, C, I, L, P, Q, V, D, E, G, H, K, T; preferably L⁽²⁾ or R⁽³⁾</entry></row><row><entry>46</entry><entry><b>E</b>, V</entry><entry><b>E</b>, D, K, Q, V, A, G, N</entry></row><row><entry>47</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> W⁽²⁾, L⁽¹⁾ or F⁽¹⁾, A, G, I, M, R, S, D, E, H, K, Q, T, V or Y; preferably W⁽²⁾, L⁽¹⁾, F⁽¹⁾ or R</entry></row><row><entry>48</entry><entry><b>V</b></entry><entry><b>V</b>, I, L, A, C, E, F, G, H, M, P, Q, R, S, T, V, W, Y</entry></row><row><entry>49</entry><entry><b>S</b>, <u>A</u>, <u>G</u></entry><entry><b>A</b>, <u>S</u>, A, G, T, V, D, E, I, L, Q, R, Y</entry></row></tbody></tgroup></table></tables><tables id="tabl0020" num="0020"><table frame="all"><title><b>Table 6: Non-limiting examples of amino acid residues in FR3 (for the footnotes, see the footnotes to Table 2)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="51mm" /><colspec colnum="3" colname="col3" colwidth="67mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>66</entry><entry><b>R</b></entry><entry><b>R</b></entry></row><row><entry>67</entry><entry><b>F</b></entry><entry><b>F</b>, L, V, A, D, I, S, Y</entry></row><row><entry>68</entry><entry><b>T</b></entry><entry><b>T</b>, A, S, D, F, G, I, K, N</entry></row><row><entry>69</entry><entry><b>I</b></entry><entry><b>I</b>, M, V, A, F, L, R, S, T</entry></row><row><entry>70</entry><entry><b>S</b></entry><entry><b>S</b>, A, F, E, G, K, P, T, V</entry></row><row><entry>71</entry><entry><b>R</b></entry><entry><b>R</b>, G, I, K, Q, S, T, W, A, F, L, M, N</entry></row><row><entry>72</entry><entry><b>D</b>, E</entry><entry><b>D</b>, E, G, N, V, A, H, I, L, Q, S, T</entry></row><row><entry>73</entry><entry><b>N</b>, <u>D</u>, G</entry><entry><b>N</b>, D, F, I, K, S, T, Y, A, G, H, L, M, R, V</entry></row><row><entry>74</entry><entry><b>A</b>, S</entry><entry><b>A</b>, D, G, N, P, S, T, F, H, I, L, R, V, Y</entry></row><row><entry>75</entry><entry><b>K</b></entry><entry><b>K</b>, A, E, K, L, N, Q, R, D, G, I, M, S, T, V, W</entry></row><row><entry>76</entry><entry><b>N</b>, S</entry><entry><b>N</b>, D, K, R, S, T, Y, E, G, H, I, Q</entry></row><row><entry>77</entry><entry><u>S</u>, <u>T</u>, I</entry><entry><b>T</b>, A, E, I, M, S, K, L, N, R, V</entry></row><row><entry>78</entry><entry><b>L</b>, A</entry><entry><b>V</b>, <u>L</u>,A, F, G, I, M, E, N, Q, R, S, T, W</entry></row><row><entry>79</entry><entry><b>Y</b>, H</entry><entry><b>Y</b>, A, D, F, H, S, T, C, E, I, L, N, V, W</entry></row><row><entry>80</entry><entry><b>L</b></entry><entry><b>L</b>, F, V, M</entry></row><row><entry>81</entry><entry><b>Q</b></entry><entry><b>Q</b>, E, R, T, G, H, I, K, L, M, N</entry></row><row><entry>82</entry><entry><b>M</b></entry><entry><b>M</b>, I, L, V, G, P, T</entry></row><row><entry>82a</entry><entry><b>N</b>, G</entry><entry><b>N</b>, D, G, H, S, T, A, E, I, K, R, V</entry></row><row><entry>82b</entry><entry><b>S</b></entry><entry><b>S</b>, <u>N</u>, D, G, R, A, C, E, F, I, K, M, P, T, V</entry></row><row><entry>82c</entry><entry><b>L</b></entry><entry><b>L</b>, P, M, T, V</entry></row></tbody></tgroup></table></tables><tables id="tabl0021" num="0021"><table frame="all"><title><b>Table 6: Non-limiting examples of amino acid residues in FR3 (continued)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="29mm" /><colspec colnum="2" colname="col2" colwidth="63mm" /><colspec colnum="3" colname="col3" colwidth="75mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>83</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> R, K⁽⁵⁾, N, E⁽⁵⁾, I, M, A, D, G, L, Q, S, T or Q; preferably K or R; most preferably K</entry></row><row><entry>84</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> P⁽⁵⁾, A, L, R, S, D, V, F, G, H, N, T, Y; preferably P</entry></row><row><entry>85</entry><entry><b>E</b>, G</entry><entry><b>E</b>, D, G, Q, A, N, R, V, Y</entry></row><row><entry>86</entry><entry><b>D</b></entry><entry><b>D</b>, E, F, Y</entry></row><row><entry>87</entry><entry><b>T</b>, M</entry><entry><b>T</b>, S, A, C, M</entry></row><row><entry>88</entry><entry><b>A</b></entry><entry><b>A</b>, <u>G</u>, S, D, L, N, P</entry></row><row><entry>89</entry><entry><b>V</b>, L</entry><entry><b>V</b>, A, D, I, L, M, N, R, T, E, F, S</entry></row><row><entry>90</entry><entry><b>Y</b></entry><entry><b>Y</b>, F, E, H, N</entry></row><row><entry>91</entry><entry><b>Y</b>, H</entry><entry><b>Y</b>, D, F, H, L, S, T, V, C, I, N, R, W</entry></row><row><entry>92</entry><entry><b>C</b></entry><entry><b>C</b></entry></row><row><entry>93</entry><entry><b>A</b>, K, T</entry><entry><b>A</b>, <u>N</u>, G, H, K, R, S, T, V, Y, E, F, I, L, M, Q</entry></row><row><entry>94</entry><entry><b>K</b>, R, T</entry><entry><b>A</b>, <u>V</u>, C, F, G, I, L, R, S, D, E, K, M, N, P, Q, T, W, Y T or K;</entry></row></tbody></tgroup></table></tables><tables id="tabl0022" num="0022"><table frame="all"><title><b>Table 7: Non-limiting examples of amino acid residues in FR4 (for the footnotes, see the footnotes to Table 2)</b></title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="49mm" /><colspec colnum="2" colname="col2" colwidth="58mm" /><colspec colnum="3" colname="col3" colwidth="59mm" /><thead><row><entry valign="top"><b>Pos.</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Amino acid residue(s):</b></entry></row><row><entry valign="top" /><entry valign="top"><i>Human V_H3</i></entry><entry valign="top"><i>Camelid V_HH's</i></entry></row></thead><tbody><row><entry>103</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> W⁽⁴⁾, P⁽⁶⁾, R⁽⁶⁾, S, F, G, K, L, N, Q, V, Y; preferably W</entry></row><row><entry>104</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> G, A, R, S, T or D; preferably G</entry></row><row><entry>105</entry><entry><b>Q</b>, <u>R</u></entry><entry><b>Q</b>, E, K, P, R, G, H, L, S, V</entry></row><row><entry>106</entry><entry><b>G</b></entry><entry><b>G</b></entry></row><row><entry>107</entry><entry><b>T</b></entry><entry><b>T</b>, A, I, N, P</entry></row><row><entry>108</entry><entry namest="col2" nameend="col3" align="left"><b><u>Hallmark residue:</u></b> Q, L⁽⁷⁾, E, H, N, P, T or R; preferably Q or L⁽⁷⁾</entry></row><row><entry>109</entry><entry><b>V</b></entry><entry><b>V</b></entry></row><row><entry>110</entry><entry><b>T</b></entry><entry><b>T</b>, I, A</entry></row><row><entry>111</entry><entry><b>V</b></entry><entry><b>V</b>, A, I, G</entry></row><row><entry>112</entry><entry><b>S</b></entry><entry><b>S</b>, F, A, L, P, T, Y</entry></row><row><entry>113</entry><entry><b>S</b></entry><entry><b>S</b>, A, L, P, F, T</entry></row></tbody></tgroup></table></tables>

0122Thus, in another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: <ol id="ol0034" compact="compact"><li>i) the Hallmark residues are as defined herein;</li></ol> and in which: <ul id="ul0047" list-style="none" compact="compact"><li>ii) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0123In another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: and in which <ol id="ol0035" compact="compact"><li>i) FR1 is chosen from the group consisting of the amino acid sequence: [1] QVQLQESGGG<b><u>X</u></b>VQAGGSLRLSCAASG [26] [SEQ ID NO: 1] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0036" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0037" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol></li></ol> and in which: <ul id="ul0048" list-style="none" compact="compact"><li>ii) FR2 is chosen from the group consisting of the amino acid sequence: [36] W<b><u>X</u></b>RQAPGK<b><u>XX</u></b>E<b><u>X</u></b>VA [49] [SEQ ID NO: 2] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0038" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0039" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: <ul id="ul0049" list-style="none" compact="compact"><li>iii) FR3 is chosen from the group consisting of the amino acid sequence: [66] RFTISRDNAKNTWLQMNSL<b><u>XX</u></b>EDTAVYYCAA [94] [SEQ ID NO: 3] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0040" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0041" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol></li></ul></li></ul> and in which: <ul id="ul0050" list-style="none" compact="compact"><li>iv) FR4 is chosen from the group consisting of the amino acid sequence: [103] <b><u>XX</u></b>QGT<b><u>X</u></b>VTSS [113] [SEQ ID NO: 4] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0042" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0043" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol></li></ul> and in which: <ul id="ul0051" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above;</li></ul> in which the Hallmark Residues are indicated by "<b><u>X</u></b>" and are as defined hereinabove and in which the numbers between brackets refer to the amino acid positions according to the Kabat numbering.

0124In another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: and in which <ol id="ol0044" compact="compact"><li>i) FR1 is chosen from the group consisting of the amino acid sequence: [1] QVQLQESGGG<b><u>L</u></b>VQAGGSLRLSCAASG [26] [SEQ ID NO: 5] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0045"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residue at position is as indicated in the sequence above; and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0046"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residue at position is as indicated in the sequence above;</li></ol></li></ol></li></ol> and in which: ii) FR2 is chosen from the group consisting of the amino acid sequences: <tables id="tabl0023" num="0023"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>L</u></b>VA [49]</entry><entry>[SEQ ID NO: 6]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>F</u></b>VA [49]</entry><entry>[SEQ ID NO: 7]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>G</u></b>A [49]</entry><entry>[SEQ ID NO: 8]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>QR</u></b>E<b><u>L</u></b>VA [49]</entry><entry>[SEQ ID NO: 9]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>QR</u></b>E<b><u>F</u></b>VA [49]</entry><entry>[SEQ ID NO: 10]</entry></row><row><entry>[36] W<b><u>Y</u></b>RQAPGK<b><u>GL</u></b>E<b><u>W</u></b>A [49]</entry><entry>[SEQ ID NO: 11]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0047" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in each of the sequences above;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0048" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in each of the sequences above;</li></ol> and in which: <ul id="ul0052" list-style="none" compact="compact"><li>iii) FR3 is chosen from the group consisting of the amino acid sequence: [66] RFTISRDNAKNTVYLQMNSL<b><u>KP</u></b>EDTAVYYCAA [94] [SEQ ID NO: 12] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the above amino acid sequence; in which <ol id="ol0049" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in each of the sequences above;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0050" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in each of the sequences above;</li></ol></li></ul> and in which: iv) FR4 is chosen from the group consisting of the amino acid sequences: <tables id="tabl0024" num="0024"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="45mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>[103] <b><u>WG</u></b>QGT<b><u>Q</u></b>VTVSS [113]</entry><entry>[SEQ ID NO: 13]</entry></row><row><entry>[103] <b><u>WG</u></b>QGT<b><u>L</u></b>VTVSS [113]</entry><entry>[SEQ ID NO: 14]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequence; in which <ol id="ol0051" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in each of the sequences above; and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0052"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in each of the sequences above;</li></ol></li></ol> and in which: <ul id="ul0053" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0125In another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: and in which <ol id="ol0053" compact="compact"><li>i) FR1 is chosen from the group consisting of the amino acid sequence: [1] QVQLQESGGG<b><u>L</u></b>VQAGGSLRLSCAASG [26] [SEQ ID NO: 5] and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0054" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residue at position is as indicated in the sequence above;</li></ol></li></ol> and in which: ii) FR2 is chosen from the group consisting of the amino acid sequences: <tables id="tabl0025" num="0025"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>L</u></b>VA [49]</entry><entry>[SEQ ID NO: 6]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>F</u></b>VA [49]</entry><entry>[SEQ ID NO: 7]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>ER</u></b>E<b><u>G</u></b>A [49]</entry><entry>[SEQ ID NO: 8]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>QR</u></b>E<b><u>L</u></b>VA [49]</entry><entry>[SEQ ID NO: 9]</entry></row><row><entry>[36] W<b><u>F</u></b>RQAPGK<b><u>QR</u></b>E<b><u>F</u></b>VA [49]</entry><entry>[SEQ ID NO: 10]</entry></row></tbody></tgroup></table></tables> and/or from the group consisting of amino acid sequences that have 2 or only I "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0055" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in each of the sequences above;</li></ol> and in which: <ul id="ul0054" list-style="none" compact="compact"><li>iii) FR3 is chosen from the group consisting of the amino acid sequence: [66] RFTISRDNAKNTVYLQMNSL<b><u>KP</u></b>EDTAVYYCAA [94] [SEQ ID NO: 12] and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0056" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in each of the sequences above;</li></ol></li></ul> and in which: iv) FR4 is chosen from the group consisting of the amino acid sequences: <tables id="tabl0026" num="0026"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="45mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>[103] <b><u>WG</u></b>QGT<b><u>Q</u></b>VTVSS [113]</entry><entry>[SEQ ID NO: 13]</entry></row><row><entry>[103] <b><u>WG</u></b>QGT<b><u>L</u></b>VTVSS [113]</entry><entry>[SEQ ID NO: 14]</entry></row></tbody></tgroup></table></tables> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0057" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 7; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in each of the sequences above;</li></ol> and in which: <ul id="ul0055" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0126In another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: and in which <ol id="ol0058" compact="compact"><li>i) FR1 is chosen from the group consisting of the amino acid sequence: [1] QVQLQESGGG<b><u>L</u></b>VQAGGSLRLSCAASG [26] [SEQ ID NO: 5] and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0059" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residue at position is as indicated in the sequence above;</li></ol></li></ol> and in which: <ul id="ul0056" list-style="none" compact="compact"><li>ii) FR2 is chosen from the group consisting of the amino acid sequence: [36] W<b><u>Y</u></b>RQAPGK<b><u>GL</u></b>E<b><u>W</u></b>A [49] [SEQ ID NO: 11] and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0060" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in each of the sequences above;</li></ol></li></ul> and in which: <ul id="ul0057" list-style="none" compact="compact"><li>iii) FR3 is chosen from the group consisting of the amino acid sequence: [66] RFTISRDNAKNTVYLQMNSL<b><u>KP</u></b>EDTAVYYCAA [94] [SEQ ID NO: 12] and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0061" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in each of the sequences above;</li></ol></li></ul> and in which: <ul id="ul0058" list-style="none" compact="compact"><li>iv) FR4 is chosen from the group consisting of the amino acid sequence: [103] <b><u>WG</u></b>QGT<b><u>Q</u></b>VTVSS [113] [SEQ ID NO: 13] and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0062" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 7; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s); and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in each of the sequences above;</li></ol></li></ul> and in which: <ul id="ul0059" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0127In another preferred, but not limiting aspect, a Nanobody of the invention can have the structure FR1 - CDR1 - FR2 - CDR2 - FR3 - CDR3 - FR4 in which FR1 to FR4 refer to framework regions 1 to 4, respectively, and in which CDR1 to CDR3 refer to the complementarity determining regions 1 to 3, respectively, and in which: and in which <ol id="ol0063" compact="compact"><li>i) FR1 is chosen from the group consisting of the FR1 sequences present in the Nanobodies of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86 to 97, or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said FR1 sequences; in which <ol id="ol0064" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR1 sequence; and</li><li>(3) the Hallmark residue at position is as indicated in said FR1 sequence;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of said FR1 sequences, in which: <ol id="ol0065" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 4; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR1 sequence; and</li><li>(3) the Hallmark residue at position is as indicated in said FR1 sequence;</li></ol></li></ol> and in which: <ul id="ul0060" list-style="none" compact="compact"><li>ii) FR2 is chosen from the group consisting of the FR2 sequences present in the Nanobodies of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86 to 97, or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said FR2 sequences; in which <ol id="ol0066" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR2 sequence; and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in said FR2 sequence;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of said FR2 sequences, in which: <ol id="ol0067" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 5; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR2 sequence; and</li><li>(3) the Hallmark residues at positions 37, 44, 45 and 47 are as indicated in said FR2 sequence;</li></ol></li></ul> and in which: <ul id="ul0061" list-style="none" compact="compact"><li>iii) FR3 is chosen from the group consisting of the FR3 sequences present in the Nanobodies of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86-97, or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said FR3 sequences; in which <ol id="ol0068" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR3 sequence; and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in said FR3 sequence;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only I "amino acid difference(s)" (as defined herein) with one of said FR3 sequences, in which: <ol id="ol0069" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR3 sequence; and</li><li>(3) the Hallmark residues at positions 83 and 84 are as indicated in said FR3 sequence;</li></ol></li></ul> and in which: <ul id="ul0062" list-style="none" compact="compact"><li>iv) FR4 is chosen from the group consisting of the FR4 sequences present in the Nanobodies of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86 to 97, or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of said FR4 sequences; in which <ol id="ol0070" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR4 sequence; and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in said FR3 sequence;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of said FR4 sequences, in which: <ol id="ol0071" compact="compact"><li>(1) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Table 6; and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to said FR4 sequence; and</li><li>(3) the Hallmark residues at positions 103, 104 and 108 are as indicated in said FR4 sequence;</li></ol></li></ul> and in which: <ul id="ul0063" list-style="none" compact="compact"><li>v) CDR1, CDR2 and CDR3 are as defined herein, and are preferably as defined according to one of the preferred definitions above, and are more preferably as defined according to one of the more preferred definitions above.</li></ul>

0128Some particularly preferred Nanobodies of the invention can be chosen from the group consisting of the amino acid sequences of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86 to 97 or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the amino acid sequences of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97 (and preferably of SEQ ID NO's 86 to 97); in which <ol id="ol0072" compact="compact"><li>(1) the Hallmark residues can be as indicated in Table 2 above;</li><li>(2) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Tables 4-7; and/or</li><li>(3) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol>

0129Some even more particularly preferred Nanobodies of the invention can be chosen from the group consisting of the amino acid sequences of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97, and in particular in the humanized Nanobodies of SEQ ID NO's 86 to 97 or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the amino acid sequences of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97 (and preferably of SEQ ID NO's 86 to 97); in which <ol id="ol0073" compact="compact"><li>(1) the Hallmark residues are as indicated in the pertinent sequence chosen from SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97 (and preferably from SEQ ID NO's 86 to 97);</li><li>(2) any amino acid substitution at any position other than a Hallmark position is preferably either a conservative amino acid substitution (as defined herein) and/or an amino acid substitution as defined in Tables 4-7; and/or</li><li>(3) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the pertinent sequence chosen from SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97 (and preferably from SEQ ID NO's 86 to 97).</li></ol>

0130Some of the most preferred Nanobodies of the invention can be chosen from the group consisting of the amino acid sequences of SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97 , and in particular from the humanized Nanobodies of SEQ ID NO's 86 to 97.

0131As will be clear from the above, the term Nanobodies of the invention as used herein in its broadest sense also comprises natural or synthetic mutants, variants, alleles, analogs and orthologs (hereinbelow collectively referred to as <i>"analogs"</i>) of the Nanobodies mentioned in the SEQ ID NO's 60 to 73 and SEQ ID NO's 86 to 97.

0132Generally, such analogs can for example comprise homologous sequences, functional portions, or a functional portion of a homologous sequence (as further defined below) of a Nanobody. Generally, in such analogs, each amino acid residue (other than the Hallmark Residue) in each of the framework regions can be replaced by any other amino acid residue, provided that the total degree of sequence identity of the framework regions remains as defined herein. Preferably, however, in such analogs: <ul id="ul0064" list-style="dash" compact="compact"><li>one or amino acid residues in the above framework sequences are replaced by one or more amino acid residues that naturally occur at the same position in a naturally occurring V_HH domain. Some examples of such substitutions are mentioned in Tables 4-7 above;</li></ul> and/or: <ul id="ul0065" list-style="dash" compact="compact"><li>one or amino acid residues in the above framework sequences are replaced by one or more amino acid residues that can be considered a "conservative" amino acid substitution, as described hereinabove;</li></ul> and/or: <ul id="ul0066" list-style="dash" compact="compact"><li>one or amino acid residues in the above framework sequences are replaced by one or more amino acid residues that naturally occur at the same position in a naturally occurring V_H domain of a human being. This is generally referred to as "humanization" of the naturally occurring V_HH/Nanobody in general and of said position in particular, and will be discussed in more detail hereinbelow;</li></ul> and: <ul id="ul0067" list-style="dash" compact="compact"><li>positions for which only one amino acid residue is mentioned for both the V_H domain and the V_HH domain in Tables 4 - 7 above are preferably not replaced.</li></ul>

0133Also, although generally less preferred, in such analogs, one or more amino acid residues may be deleted from the framework regions and/or inserted into the framework regions (optionally in addition to one or more amino acid substitutions as mentioned above), provided that the total degree of sequence identity of the framework regions remains as defined herein. The Hallmark residues should not be deleted. Also, most preferably, amino acid residues for which only one amino acid residue is mentioned for both the V_H domain and the V_HH domain in Tables 4 - 7 above are preferably not deleted.

0134Preferably, such analogs should be such that they still can bind to, have affinity for and/or have specificity for vWF, i.e. with an affinity and/or a specificity which is at least 10%, preferably at least 50%, more preferably at least 70%, even more preferably at least 80%, such as at least 90%, at least 95%, at least 99% or more, of the affinity and/or specificity of at least one of the Nanobodies of SEQ ID No's 60 to 73 and SEQ ID NO's 86 to 97, as determined using a suitable assay, for example an assay to determine binding of the analog to vWF, and in particular one of the assays as used in the Examples below.

0135Generally, such analogs can for example be obtained by providing a nucleic acid that encodes a naturally occurring V_HH domain, changing the codons for the one or more amino acid residues that are to be humanized into the codons for the corresponding human amino acid residue(s), expressing the nucleic acid/nucleotide sequence thus obtained in a suitable host or expression system; and optionally isolating and/or purifying the analog thus obtained to provide said analog in essentially isolated form (as defined hereinabove). This can generally be performed using methods and techniques known per se, which will be clear to the skilled person, for example from the handbooks and references cited herein and/or from the further description hereinbelow. Alternatively, and for example, a nucleic acid encoding an analog can be synthesized in a manner known per se (for example using an automated apparatus for synthesizing nucleic acid sequences with a predefined amino acid sequence) and can be expressed in a suitable host or expression system, upon which the analog thus obtained can optionally be isolated and/or purified so as to provide said analog in essentially isolated form (as defined hereinabove). Another way to provide the analogs involves chemical synthesis of the pertinent amino acid sequence using techniques for peptide synthesis known per se, such as those mentioned hereinbelow.

0136It will be also generally be clear to the skilled person that Nanobodies (including analogs thereof) can also be prepared starting from human V_H sequences (i.e. amino acid sequences or the corresponding nucleotide sequences), such as for example human V_H3 sequences such as DP-47, DP-51 or DP-29, by changing one or more amino acid residues in the amino acid sequence of said human V_H domain, so as to provide an amino acid sequence that has (a) a Q at position 108; and/or (b) E at position 44 and/or R at position 45, and preferably E at position 44 and R at position 45; and/or (c) P, R or S at position 103, as described above. Again, this can generally be performed using the various methods and techniques referred to in the previous paragraph, using an amino acid sequence and/or nucleotide sequence for a human V_H domain as a starting point.

0137The term Nanobodies as used herein in its broadest sense also comprises parts or fragments of the Nanobodies (including analogs) of the invention as defined herein, which can again be as further described below.

0138Generally, parts or fragments of the Nanobodies and/or analogs have amino acid sequences in which, compared to the amino acid sequence of the corresponding full length Nanobody or analog, one or more of the amino acid residues at the N-terminal end, one or more amino acid residues at the C-terminal end, one or more contiguous internal amino acid residues, or any combination thereof, have been deleted and/or removed. It is also possible to combine one or more of such parts or fragments to provide a Nanobody of the invention.

0139Preferably, the amino acid sequence of a Nanobody that comprises one or more parts or fragments of a full length Nanobody and/or analog should have a degree of sequence identity of at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, at least 90% or at least 95%, with the amino acid sequence of the corresponding full length Nanobody.

0140Also, the amino acid sequence of a Nanobody that comprises one or more parts or fragments of a full length Nanobody and/or analog is preferably such that is comprises at least 10 contiguous amino acid residues, preferably at least 20 contiguous amino acid residues, more preferably at least 30 contiguous amino acid residues, such as at least 40 contiguous amino acid residues, of the amino acid sequence of the corresponding full length Nanobody.

0141Generally, such parts or fragments of the Nanobodies of the invention will have amino acid sequences in which, compared to the amino acid sequence of the corresponding full length Nanobody of the invention, one or more of the amino acid residues at the N-terminal end, one or more amino acid residues at the C-terminal end, one or more contiguous internal amino acid residues, or any combination thereof, have been deleted and/or removed. It is also possible to combine one or more of such parts or fragments to provide a Nanobody of the invention.

0142According to one preferred embodiment, a fragment as used herein comprises at least one of the CDR's present in a full-sized Nanobody of the invention, preferably at least two of the CDR's present in a full-sized Nanobody of the invention, more preferably at least CDR2 and CDR3 present in a full-sized Nanobody of the invention, such as for example all three CDR's present in a full-sized Nanobody of the invention.

0143According to another particularly preferred, but non-limiting embodiment, such a part or fragment comprises at least FR3, CDR3 and FR4 of the corresponding full length Nanobody of the invention, i.e. as for example described in the International application <patcit id="pcit0068" dnum="WO03050531A"><text>WO 03/050531 (Lasters et al.</text></patcit>).

0144Preferably, such parts or fragments should be such that they still can bind to, have affinity for and/or have specificity for vWF, i.e. with an affinity and/or a specificity which is at least 10%, preferably at least 50%, more preferably at least 70%, even more preferably at least 80%, such as at least 90%, at least 95%, at least 99% or more, of the affinity and/or specificity of the corresponding full-sized Nanobody of the invention, for example an assay to determine binding of the analog to vWF, and in particular one of the assays as used in the Examples below.

0145From the description hereinabove, it will be clear that the amino acid sequences of the Nanobodies used herein differ at at least one amino acid position in at least one of the framework regions from the amino acid sequences of naturally occurring V_H domains, such as the amino acid sequences of naturally occurring V_H domains of antibodies from human beings. In particular, it will be clear that the amino acid sequences of the Nanobodies used herein differ at at least one of the Hallmark Residues from amino acid sequences of naturally occurring V_H domains, such as the amino acid sequences of naturally occurring V_H domains from antibodies from Camelids and/or human beings.

0146Thus, according to one specific embodiment, a Nanobody of the invention has an amino acid sequence that differs at at least one amino acid position in one of the framework regions from the amino acid sequence of a naturally occurring V_H domain. According to a more specific, but non-limiting embodiment of the invention, a Nanobody of the invention has an amino acid sequence that differs at at least one of the Hallmark residues from the amino acid sequence of a naturally occurring V_H domain.

0147From the description hereinabove, it will also be clear that the amino acid sequences of the some of the Nanobodies of the invention, such as the humanized Nanobodies of the invention, will differ at at least one amino acid position in at least one of the framework regions (i.e. either at the position of a Hallmark residue or at another position) from the amino acid sequences of naturally occurring V_HH domains. Thus, according to one specific, but non-limiting embodiment, a Nanobody of the invention has an amino acid sequence that differs at at least one amino acid position in one of the framework regions from the amino acid sequence of a naturally occurring V_HH domain. According to a more specific, but non-limiting embodiment of the invention, a Nanobody of the invention has an amino acid sequence that differs at at least one of the Hallmark residues from the amino acid sequence of a naturally occurring V_HH domain.

0148As mentioned above, the invention also relates to proteins or polypeptides comprising at least one V_HH domain (i.e. as identified using the methods of the invention) or at least one Nanobody based thereon.

0149According to one non-limiting embodiment of the invention, such a polypeptide of the invention essentially consists of a Nanobody. By "essentially consist of" is meant that the amino acid sequence of the polypeptide of the invention either is exactly the same as the amino acid sequence of a Nanobody (as mentioned above) or corresponds to the amino acid sequence of a Nanobody in which a limited number of amino acid residues, such as 1-10 amino acid residues and preferably 1-6 amino acid residues, such as 1, 2, 3, 4, 5 or 6 amino acid residues, have been added to the amino terminal end, to the carboxy terminal end, or both to the amino terminal end and to the carboxy terminal end of the amino acid sequence of the Nanobody.

0150Said amino acid residues may or may not change, alter or otherwise influence the (biological) properties of the Nanobody and may or may not add further functionality to the Nanobody. For example, said amino acid residues may: <ol id="ol0074" compact="compact"><li>a) form a "tag", i.e. an amino acid sequence or residue that allows or facilitates the purification of the Nanobody, for example using affinity techniques directed against said sequence or residue. Thereafter, said sequence or residue may be removed (e.g. by chemical or enzymatical cleavage) to provide the nucleotide sequence of the invention (for this purpose, the sequence or residue may optionally be linked to the amino acid sequence of the invention via a cleavable linker sequence). Some preferred, but non-limiting examples of such residues are multiple histidine residues and glutatione residues,</li><li>b) can be a N-terminal Met residue, for example as result of expression in a heterologous host cell or host organism.</li><li>c) may be one or more amino acid residues that can be provided with functional groups and/or that have been functionalized, in a manner known per se. For example, as is known in the art, amino acid residues such as lysine and in particular cysteine allow for the attachment of PEG groups, which may mask surface site on a protein and thus for example decrease immunogenicity, improve half-life in plasma and stabilize against proteolytic cleavage;</li><li>d) increase the half-life in serum of a Nanobody or polypeptide of the invention. Amino acid sequences that can be attached to and/or fused with therapeutic proteins in order to increase their half-life in vivo are well know to the skilled person and include human serum proteins or fragments thereof (such as human serum albumin or a part or fragment thereof), or even Fc portions of antibodies (in particular of human antibodies). Also, as already described herein, such an amino acid sequence for increasing the half-life may be an amino acid sequence directed against a serum protein, such as a Nanobody directed against a serum protein, for example against human serum albumin.</li></ol>

0151With regard to pegylation, its should be noted that generally, the invention also encompasses any Nanobody of the invention and/or polypeptide of the invention that has been pegylated at one or more amino acid positions, preferably in such a way that said pegylation either (1) increases the half-life in vivo; (2) reduces immunogenicity; (3) provides one or more further beneficial properties known per se for pegylation; (4) does not essentially affect the affinity of the Nanobody and/or polypeptide for vWF (e.g. does not reduce said affinity by more than 90%, preferably not by more than 50 %, and more preferably not by more than 10%, as determined by a suitable assay, such as those described in the Examples below); and/or (4) does not affect any of the other desired properties of the Nanobodies and/or polypeptides of the invention. Suitable PEG-groups and methods for attaching them, either specifically or non-specifically, will be clear to the skilled person. Suitable kits and reagents for such pegylation can for example be obtained from Nektar (CA, USA).

0152According to one non-limiting embodiment, one or more amino acid residues can be added to, inserted in and/or substituted in the amino acid sequence of a Nanobody or polypeptide of the invention, so as to provide one or more specific amino acid residues for attachment of a PEG-group.

0153The invention also encompasses any Nanobody of the invention and/or polypeptide of the invention that has been glycosylated at one or more amino acid positions, usually depending upon the host used to express the Nanobody or polypeptide of the invention (as further described below).

0154According to one non-limiting embodiment, one or more amino acid residues can be added to, inserted in and/or substituted in the amino acid sequence of a Nanobody or polypeptide of the invention, so as to provide one or more specific amino acid residues and/or a site that can be glycosylated by the host organism used. By means of a preferred, but non-limiting example, the N-residue on position 50 within CDR2 of a Nanobody of the invention can for example be replaced by a Q, D or S residue so as to provide a glycosylation site, e.g. for glycosylation by <i>Pichia.</i>

0155According to another embodiment, a polypeptide of the invention can comprise a the amino acid sequence of a Nanobody, which is fused at its amino terminal end, at its carboxy terminal end, or both at its amino terminal end and at its carboxy terminal end with at least one further amino acid sequence.

0156Again, said further amino acid sequence(s) may or may not change, alter or otherwise influence the (biological) properties of the Nanobody and may or may not add further functionality to the Nanobody.

0157For example, according to one preferred, but non-limiting embodiment, said further amino acid sequence may comprise at least one further Nanobody, so as to provide a polypeptide of the invention that comprises at least two, such as three, four or five, Nanobodies, in which said Nanobodies may optionally be linked via one or more linker sequences (as defined herein).

0158Polypeptides of the invention comprising two or more Nanobodies will also referred to herein as "multivalent" polypeptides. For example a "bivalent" polypeptide of the Invention comprises two Nanobodies, optionally linked via a linker sequence, whereas a "trivalent" polypeptide of the invention comprises three Nanobodies, optionally linked via two linker sequences; etc.

0159In a multivalent polypeptide of the invention, the two or more Nanobodies may be the same or different. For example, the two or more Nanobodies in a multivalent polypeptide of the invention: <ul id="ul0068" list-style="dash" compact="compact"><li>may be directed against the same antigen, i.e. against the same parts or epitopes of said antigen or against two or more different parts or epitopes of said antigen; and/or:</li><li>may be directed against the different antigens;</li></ul> or a combination thereof.

0160Thus, a bivalent polypeptide of the invention for example: <ul id="ul0069" list-style="dash" compact="compact"><li>may comprise two identical Nanobodies;</li><li>may comprise a first Nanobody directed against a first part or epitope of an antigen and a second Nanobody directed against the same part or epitope of said antigen or against another part or epitope of said antigen;</li><li>or may comprise a first Nanobody directed against a first antigen and a second Nanobody directed against a second antigen different from said first antigen;</li></ul> whereas a trivalent Polypeptide of the Invention for example: <ul id="ul0070" list-style="dash" compact="compact"><li>may comprises three identical or different Nanobodies directed against the same or different parts or epitopes of the same antigen;</li><li>may comprise two identical or different Nanobodies directed against the same or different parts or epitopes on a first antigen and a third Nanobody directed against a second antigen different from said first antigen; or</li><li>may comprise a first Nanobody directed against a first antigen, a second Nanobody directed against a second antigen different from said first antigen, and a third Nanobody directed against a third antigen different from said first and second antigen,</li></ul>

0161Polypeptides of the invention that contain at least two Nanobodies, in which at least one Nanobody is directed against a first antigen and at least one Nanobody is directed against a second Nanobody different from the first antigen, will also be referred to as "multispecific" Nanobodies. Thus, a "bispecific" Nanobody is a Nanobody that comprises at least one Nanobody directed against a first antigen and at least one further Nanobody directed against a second antigen, whereas a "trispecific" Nanobody is a Nanobody that comprises at least one Nanobody directed against a first antigen, at least one further Nanobody directed against a second antigen, and at least one further Nanobody directed against a third antigen; etc.

0162Accordingly, in their simplest form, a bispecific polypeptide of the invention is a bivalent polypeptide of the invention (as defined herein), comprising a first Nanobody directed against a first antigen and a second Nanobody directed against a second antigen, in which said first and second Nanobody may optionally be linked via a linker sequence (as defined herein); whereas a trispecific polypeptide of the invention in its simplest form is a trivalent polypeptide of the invention (as defined herein), comprising a first Nanobody directed against a first antigen, a second Nanobody directed against a second antigen and a third Nanobody directed against a third antigen, in which said first, second and third Nanobody may optionally be linked via one or more, and in particular one and more in particular two, linker sequences.

0163However, as will be clear from the description hereinabove, the invention is not limited thereto, in the sense that a multispecific polypeptide of the invention may comprise any number of Nanobodies directed against two or more different antigens.

0164For multivalent and multispecific polypeptides containing one or more V_HH domains and their preparation, reference is also made to <nplcit id="ncit0104" npl-type="s"><text>Conrath et al., J. Biol. Chem., Vol. 276, 10. 7346-7350</text></nplcit>, as well as to <patcit id="pcit0069" dnum="EP0822985A"><text>EP 0 822 985</text></patcit>.

0165Linkers for use in multivalent and multispecific polypeptides will be clear to the skilled person, and for example include gly-ser linkers, for example of the type (gly_xser_y)_z, such as (for example (gly₄ser)₃ or (gly₃ser₂)₃, as described in <patcit id="pcit0070" dnum="WO9942077A"><text>WO 99/42077</text></patcit>, hinge like regions such as the hinge regions of naturally occurring heavy chain antibodies or similar sequences. For other suitable linkers, reference is also made to the general background art cited above. Some particularly preferred linkers are given in SEQ ID NO's 83 to 85, in which the linkers of SEQ ID NO's 84 and 85 are particularly preferred.

0166Linkers can also provide some functionality for the multivalent or multispecific polypeptide. For example, linkers containing one or more charged amino acid residues (see Table 1 above) can provide improved hydrophilic properties, whereas linkers that form or contain small epitopes or tags can be used for the purposes of detection, identification and/or purification.

0167As also further described herein, a multispecific polypeptide of the invention directed against a desired antigen and against at least one serum protein, such as the serum proteins mentioned hereinbelow, and in particular against human serum albumin, may show increased half-life in serum, compared to the corresponding monovalent Nanobody.

0168As mentioned hereinabove, the methods described herein are particularly suited for generating such multivalent of multispecific polypeptides of the invention.

0169In a polypeptide of the invention, the at least one Nanobody may also be linked to a conventional V_H domain or to a natural or synthetic analog of a V_H domain, optionally via a linker sequence.

0170In a polypeptide of the invention, the at least one Nanobody may also be linked to a V_L domain or to a natural or synthetic analog of a V_L domain, optionally via a linker sequence, so as to provide a polypeptide of the invention that is in the form analogous to a conventional scFv fragment but containing a Nanobody instead of a V_H domain.

0171In a polypeptide of the invention, the at least one Nanobody may also be linked to one or more of a CHI, CH2 and/or CH3 domain, optionally via a linker sequence. For instance, a Nanobody linked to a suitable CH1 domain could for example be used - together with suitable light chains - to generate antibody fragments/structures analogous to conventional Fab fragments or F(ab')₂ fragments, but in which one or (in case of an F(ab')₂ fragment) one or both of the conventional V_H domains have been replaced by a Nanobody. Such fragments may also be heterospecific or bispecific, i.e. directed against two or more antigens. A Nanobody linked to suitable CH2 and CH3 domains, for example derived from Camelids, could be used to form a monospecific or bispecific heavy chain antibody. Finally, a Nanobody linked to suitable CHI, CH2 and CH3 domains, for example derived from a human being, could be used - together with suitable light chains - to form an antibody that is analogous to a conventional 4-chain antibody, but in which one or both of the conventional V_H domains have been replaced by a Nanobody.

0172Also, in addition to the one or more Nanobodies, Polypeptides of the Invention can also contain functional groups, moieties or residues, for example therapeutically active substances, such as those mentioned below, and/or markers or labels, such as fluorescent markers, isotopes, etc., as further described hereinbelow.

0173The Nanobodies of the invention, the polypeptides of the invention, and nucleic acids encoding the same, can be prepared in a manner known per se, asd will be clear to the skilled person from the further description herein. Some preferred, but non-limiting methods for preparing the Nanobodies, polypeptides and nucleic acids include the methods and techniques mentioned above and/or further described hereinbelow .

0174As will be clear to the skilled person, one particularly useful method for preparing a Nanobody and/or a polypeptide of the invention generally comprises the steps of: <ul id="ul0071" list-style="dash" compact="compact"><li>the expression, in a suitable host cell or host organism (also referred to herein as a <i>"host of the invention</i>") or in another suitable expression system of a nucleic acid that encodes said Nanobody or polypeptide of the invention (also referred to herein as a <i>"nucleic acid of the invention"</i>), optionally followed by:</li><li>isolating and/or purifying the Nanobody or polypeptide of the invention thus obtained.</li></ul>

0175In particular, such a method may comprise the steps of: <ul id="ul0072" list-style="dash" compact="compact"><li>cultivating and/or maintaining a host of the invention under conditions that are such that said host of the invention expresses and/or produces at least one Nanobody and/or polypeptide of the invention; optionally followed by:</li><li>isolating and/or purifying the Nanobody or polypeptide of the invention thus obtained.</li></ul>

0176A nucleic acid of the invention can be in the form of single or double stranded DNA or RNA, and is preferably in the form of double stranded DNA. For example, the nucleotide sequences of the invention may be genomic DNA, cDNA or synthetic DNA (such as DNA with a codon usage that has been specifically adapted for expression in the intended host cell or host organism).

0177According to one embodiment of the invention, the nucleic acid of the invention is in essentially isolated from, as defined hereinabove.

0178The nucleic acid of the invention may also be in the form of, be present in and/or be part of a vector, such as for example a plasmid, cosmid or YAC, which again may be in essentially isolated form.

0179The nucleic acids of the invention can be prepared or obtained in a manner known per se, based on the information on the amino acid sequences for the polypeptides of the invention given herein, and/or can be isolated from a suitable natural source. To provide analogs, nucleotide sequences encoding naturally occurring V_HH domains can for example be subjected to site-directed mutagenesis, so at to provide a nucleic acid of the invention encoding said analog. Also, as will be clear to the skilled person, to prepare a nucleic acid of the invention, also several nucleotide sequences, such as at least one nucleotide sequence encoding a Nanobody and for example nucleic acids encoding one or more linkers can be linked together in a suitable manner.

0180Techniques for generating the nucleic acids of the invention will be clear to the skilled person and may for instance include, but are not limited to, automated DNA synthesis; site-directed mutagenesis; combining two or more naturally occurring and/or synthetic sequences (or two or more parts thereof), introduction of mutations that lead to the expression of a truncated expression product; introduction of one or more restriction sites (e.g. to create casettes and/or regions that may easily be digested and/or ligated using suitable restriction enzymes), and/or the introduction of mutations by means of a PCR reaction using one or more "mismatched" primers, using for example a sequence of a naturally occurring GPCR as a template. These and other techniques will be clear to the skilled person, and reference is again made to the standard handbooks, such as Sambrook et al. and Ausubel et al., mentioned above, as well as the Examples below.

0181The nucleic acid of the invention may also be in the form of, be present in and/or be part of a genetic construct, as will be clear to the person skilled in the art. Such genetic constructs generally comprise at least one nucleic acid of the invention that is optionally linked to one or more elements of genetic constructs known per se, such as for example one or more suitable regulatory elements (such as a suitable promoters), enhancer(s), terminator(s), etc.) and the further elements of genetic constructs referred to hereinbelow. Such genetic constructs comprising at least one nucleic acid of the invention will also be referred to herein as <i>"genetic constructs of the invention".</i>

0182The genetic constructs of the invention may be DNA or RNA, and are preferably double-stranded DNA. The genetic constructs of the invention may also be in a form suitable for transformation of the intended host cell or host organism, in a form suitable for integration into the genomic DNA of the intended host cell or in a form suitable independent replication, maintenance and/or inheritance in the intended host organism. For instance, the genetic constructs of the invention may be in the form of a vector, such as for example a plasmid, cosmid, YAC, a viral vector or transposon. In particular, the vector may be an expression vector, i.e. a vector that can provide for expression <i>in vitro</i> and/or <i>in vivo</i> (e.g. in a suitable host cell, host organism and/or expression system).

0183In a preferred but non-limiting embodiment, a genetic construct of the invention comprises <ol id="ol0075" compact="compact"><li>a) at least one nucleic acid of the invention; operably connected to</li><li>b) one or more regulatory elements, such as a promoter and optionally a suitable terminator;</li><li>c) and optionally also</li><li>d) one or more further elements of genetic constructs known per se;</li></ol> in which the terms "regulatory element", "promoter", "terminator" and "operably connected" have their usual meaning in the art (as further described below); and in which said "further elements" present in the genetic constructs may for example be 3'- or 5'-UTR sequences, leader sequences, selection markers, expression markers/reporter genes, and/or elements that may facilitate or increase (the efficiency of) transformation or integration. These and other suitable elements for such genetic constructs will be clear to the skilled person, and may for instance depend upon the type of construct used, the intended host cell or host organism; the manner in which the nucleotide sequences of the invention of interest are to be expressed (e.g. via constitutive, transient or inducible expression); and/or the transformation technique to be used.

0184Preferably, in the genetic constructs of the invention, said at least one nucleic acid of the invention and said regulatory elements, and optionally said one or more further elements, are "operably linked" to each other, by which is generally meant that they are in a functional relationship with each other. For instance, a promoter is considered "operably linked" to a coding sequence if said promoter is able to initiate or otherwise control/regulate the transcription and/or the expression of a coding sequence (in which said coding sequence should be understood as being "under the control of" said promoter). Generally, when two nucleotide sequences are operably linked, they will be in the same orientation and usually also in the same reading frame. They will usually also be essentially contiguous, although this may also not be required.

0185Preferably, the regulatory and further elements of the genetic constructs of the invention are such that they are capable of providing their intended biological function in the intended host cell or host organism.

0186For instance, a promoter, enhancer or terminator should be <i>"operable"</i> in the intended host cell or host organism, by which is meant that (for example) said promoter should be capable of initiating or otherwise controlling/regulating the transcription and/or the expression of a nucleotide sequence - e.g. a coding sequence - to which it is operably linked (as defined herein).

0187Some particularly preferred promoters include, but are not limited to, promoters known per se for the expression in bacterial cells, such as those mentioned hereinbelow and/or those used in the Examples.

0188A selection marker should be such that it allows - i.e. under appropriate selection conditions - host cells and/or host organisms that have been (succesfully) transformed with the nucleotide sequence of the invention to be distinguished from host cells/organisms that have not been (succesfully) transformed. Some preferred, but non-limiting examples of such markers are genes that provide resistance against antibiotics (such as kanamycine or ampicilline), genes that provide for temperature resistance, or genes that allow the host cell or host organism to be maintained in the absence of certain factors, compounds and/or (food) components in the medium that are essential for survival of the non-transformed cells or organisms.

0189A leader sequence should be such that - in the intended host cell or host organism - it allows for the desired post-translational modifications and/or such that it directs the transcribed mRNA to a desired part or organelle of a cell. A leader sequence may also allow for secretion of the expression product from said cell. As such, the leader sequence may be any pro-, pre-, or prepro-sequence operable in the host cell or host organism. Leader sequences may not be required for expression in a bacterial cell.

0190An expression marker or reporter gene should be such that - in the host cell or host organism - it allows for detection of the expression of (a gene or nucleotide sequence present on) the genetic construct. An expression marker may optionally also allow for the localisation of the expressed product, e.g. in a specific part or organelle of a cell and/or in (a) specific cell(s), tissue(s), organ(s) or part(s) of a multicellular organism. Such reporter genes may also be expressed as a protein fusion with the amino acid sequence of the invention. Some preferred, but non-limiting examples include fluorescent proteins such as GFP.

0191Some preferred, but non-limiting examples of suitable promoters, terminator and further elements include those used in the Examples below. For some (further) non-limiting examples of the promoters, selection markers, leader sequences, expression markers and further elements that may be present/used in the genetic constructs of the invention - such as terminators, transcriptional and/or translational enhancers and/or integration factors - reference is made to the general handbooks such as Sambrook et al. and Ausubel et al. mentioned above, as well as to the examples that are given in <patcit id="pcit0071" dnum="WO9507463A"><text>WO 95/07463</text></patcit>, <patcit id="pcit0072" dnum="WO9623810A"><text>WO 96/23810</text></patcit>, <patcit id="pcit0073" dnum="WO9507463A"><text>WO 95/07463</text></patcit>, <patcit id="pcit0074" dnum="WO9521191A"><text>WO 95/21191</text></patcit>, <patcit id="pcit0075" dnum="WO9711094A"><text>WO 97/11094</text></patcit>, <patcit id="pcit0076" dnum="WO9742320A"><text>WO 97/42320</text></patcit>, <patcit id="pcit0077" dnum="WO9806737A"><text>WO 98/06737</text></patcit>, <patcit id="pcit0078" dnum="WO9821355A"><text>WO 98/21355</text></patcit>, <patcit id="pcit0079" dnum="US6207410A"><text>US-A-6,207,410</text></patcit>, <patcit id="pcit0080" dnum="US5693492A"><text>US-A- 5,693,492</text></patcit> and <patcit id="pcit0081" dnum="EP1085089A"><text>EP 1 085 089</text></patcit>. Other examples will be clear to the skilled person. Reference is also made to the general background art cited above and the further references cited hereinbelow.

0192The genetic constructs of the invention may generally be provided by suitably linking the nucleotide sequence(s) of the invention to the one or more further elements described above, for example using the techniques described in the general handbooks such as Sambrook et al. and Ausubel et al., mentioned above.

0193Often, the genetic constructs of the invention will be obtained by inserting a nucleotide sequence of the invention in a suitable (expression) vector known per se. Some preferred, but non-limiting examples of suitable expression vectors are those used in the Examples below, as well as those mentioned below.

0194The nucleic acids of the invention and/or the genetic constructs of the invention may be used to transform a host cell or host organism, i.e. for expression and/or production of the Nanobody or polypeptide of the invention. Suitable hosts or host cells will be clear to the skilled person, and may for example be any suitable fungal, prokaryotic or eukaryotic cell or cell line or any suitable fungal, prokaryotic or eukaryotic organism, for example: <ul id="ul0073" list-style="dash" compact="compact"><li>a bacterial strain, including but not limited to gram-negative strains such as strains of <i>Escherichia coli</i>; of <i>Proteus,</i> for example of <i>Proteus mirabilis;</i> of <i>Pseudomonas,</i> for example of <i>Pseudomonas fluoresceins</i>; and gram-positive strains such as strains of <i>Bacillus,</i> for example of <i>Bacillus subtilis</i> or of <i>Bacillus brevis;</i> of <i>Streptomyces,</i> for example of <i>Streptomyces lividans</i>; of <i>Staphylococcus,</i> for example of <i>Staphylococcus carnosus</i>; and of <i>Lactococcus</i>, for example of <i>Lactococcus lactis;</i></li><li>a fungal cell, including but not limited to cells from species of <i>Trichoderma,</i> for example from <i>Trichoderma reesei;</i> of <i>Neurospora,</i> for example from <i>Neurospora crassa</i>; of <i>Sordaria</i>, for example from <i>Sordaria macrospora</i>; of <i>Aspergillus,</i> for example from <i>Aspergillus niger</i> or from <i>Aspergillus sojae;</i> or from other filamentous fungi;</li><li>a yeast cell, including but not limited to cells from species of <i>Saccharomyces,</i> for example of <i>Saccharomyces cerevisiae</i>; of <i>Schizosaccharomyces,</i> for example of <i>Schizosaccharomyces pombe</i>; of <i>Pichia,</i> for example of <i>Pichia pastoris</i> or of <i>Pichia methanolica;</i> of <i>Hansenula,</i> for example of <i>Hansenula polymorpha;</i> of <i>Kluyveromyces</i>, for example of <i>Kluyveromyces lactis;</i> of <i>Arxula,</i> for example of <i>Arxula adeninivorans</i>; of <i>Yarrowia</i>, for example of <i>Yarrowia lipolytica;</i></li><li>an amphibian cell or cell line, such as <i>Xenopus oocytes</i>;</li><li>an insect-derived cell or cell line, such as cells/cell lines derived from lepidoptera, including but not limited to <i>Spodoptera</i> SF9 and Sf21 cells or cells/cell lines derived from <i>Drosophila,</i> such as Schneider and Kc cells;</li><li>a plant or plant cell, for example in tobacco plants; and/or</li><li>a mammalian cell or cell line, for example derived a cell or cell line derived from a human, from the mammals including but not limited to CHO-cells, BHK-cells (for example BHK-21 cells) and human cells or cell lines such as HeLa, COS (for example COS-7) and PER.C6 cells;</li></ul> as well as all other hosts or host cells known per se for the expression and production of antibodies and antibody fragments (including but not limited to (single) domain antibodies and ScFv fragments), which will be clear to the skilled person. Reference is also made to the general background art cited hereinabove, as well as to for example <patcit id="pcit0082" dnum="WO9429457A"><text>WO 94/29457</text></patcit>; <patcit id="pcit0083" dnum="WO9634103A"><text>WO 96/34103</text></patcit>; <patcit id="pcit0084" dnum="WO9942077A"><text>WO 99/42077</text></patcit>; Frenken et al., (1998), supra; Riechmann and Muyldermans, (1999), supra; van der Linden, (2000), supra; Thomassen et al., (2002), supra; Joosten et al., (2003), supra; Joosten et al., (2005), supra; and the further references cited herein.

0195The Nanobodies and polypeptides of the invention can also be introduced and expressed in one or more cells, tissues or organs of a multicellular organism, for example for prophylactic and/or therapeutic purposes (e.g. as a gene therapy). For this purpose, the nucleotide sequences of the invention may be introduced into the cells or tissues in any suitable way, for example as such (e.g. using liposomes) or after they have been inserted into a suitable gene therapy vector (for example derived from retroviruses such as adenovirus, or parvoviruses such as adeno-associated virus). As will also be clear to the skilled person, such gene therapy may be performed <i>in vivo</i> and/or <i>in situ</i> in the body of a patent by administering a nucleic acid of the invention or a suitable gene therapy vector encoding the same to the patient or to specific cells or a specific tissue or organ of the patient; or suitable cells (often taken from the body of the patient to be treated, such as explanted lymphocytes, bone marrow aspirates or tissue biopsies) may be treated in vitro with a nucleotide sequence of the invention and then be suitably (re-)introduced into the body of the patient. All this can be performed using gene therapy vectors, techniques and delivery systems which are well known to the skilled person, for <nplcit id="ncit0105" npl-type="b"><text>Culver, K. W., "Gene Therapy", 1994, p. xii, Mary Ann Liebert, Inc., Publishers, New York, N.Y</text></nplcit>). <nplcit id="ncit0106" npl-type="s"><text>Giordano, Nature F Medicine 2 (1996), 534-539</text></nplcit>; <nplcit id="ncit0107" npl-type="s"><text>Schaper, Circ. Res. 79 (1996), 911-919</text></nplcit>; <nplcit id="ncit0108" npl-type="s"><text>Anderson, Science 256 (1992),808-813</text></nplcit>; <nplcit id="ncit0109" npl-type="s"><text>Verma, Nature 389 (1994),239</text></nplcit>; <nplcit id="ncit0110" npl-type="s"><text>Isner, Lancet 348 (1996),370-374</text></nplcit>; <nplcit id="ncit0111" npl-type="s"><text>Muhlhauser, Circ. Res. 77 (1995),1077-1086</text></nplcit>; <nplcit id="ncit0112" npl-type="s"><text>Onodera, Blood 91; (1998),30- 36</text></nplcit>; <nplcit id="ncit0113" npl-type="s"><text>Verma, Gene Ther. 5 (1998),692-699</text></nplcit>; <nplcit id="ncit0114" npl-type="s"><text>Nabel, Ann. N.Y. Acad. Sci. : 811 (1997), 289-292</text></nplcit>; <nplcit id="ncit0115" npl-type="s"><text>Verzeletti, Hum. Gene Ther. 9 (1998), 2243-51</text></nplcit>; <nplcit id="ncit0116" npl-type="s"><text>Wang, Nature Medicine 2 (1996),714-716</text></nplcit>; <patcit id="pcit0085" dnum="WO9429469A"><text>WO 94/29469</text></patcit>; <patcit id="pcit0086" dnum="WO9700957A"><text>WO 97/00957</text></patcit>, <patcit id="pcit0087" dnum="US5580859A"><text>US 5,580,859</text></patcit>; 1 <patcit id="pcit0088" dnum="US55895466B"><text>US 5,5895466</text></patcit>; or <nplcit id="ncit0117" npl-type="s"><text>Schaper, Current Opinion in Biotechnology 7 (1996), 635-640</text></nplcit>. For example, in situ expression of ScFv fragments (<nplcit id="ncit0118" npl-type="s"><text>Afanasieva et al., Gene Ther., 10, 1850-1859 (2003</text></nplcit>)) and of diabodies (<nplcit id="ncit0119" npl-type="s"><text>Blanco et al., J. Immunol, 171, 1070-1077 (2003</text></nplcit>)) has been described in the art.

0196For expression of the Nanobodies in a cell, they may also be expressed as so-called or as so-called "intrabodies", as for example described in <patcit id="pcit0089" dnum="WO9402610A"><text>WO 94/02610</text></patcit>, <patcit id="pcit0090" dnum="WO9522618A"><text>WO 95/22618</text></patcit> and <patcit id="pcit0091" dnum="US7004940A"><text>US-A-7004940</text></patcit>; <patcit id="pcit0092" dnum="WO03014960A"><text>WO 03/014960</text></patcit>; in <nplcit id="ncit0120" npl-type="b"><text>Cattaneo, A. &amp; Biocca, S. (1997) Intracellular Antibodies: Development and Applications. Landes and Springer-Verlag</text></nplcit>; and in <nplcit id="ncit0121" npl-type="s"><text>Kontermann, Methods 34, (2004), 163-170</text></nplcit>.

0197For production, the Nanobodies and polypeptides of the invention can for example also be produced in the milk of transgenic mammals, for example in the milk of rabbits, cows, goats or sheep (see for example <patcit id="pcit0093" dnum="US6741957A"><text>US-A-6,741,957</text></patcit>, <patcit id="pcit0094" dnum="US6304489A"><text>US-A-6,304,489</text></patcit> and <patcit id="pcit0095" dnum="US6849992A"><text>US-A-6,849,992</text></patcit> for general techniques for introducing transgenes into mammals), in plants or parts of plants including but not limited to their leaves, flowers, fruits, seed, roots or turbers (for example in tobacco, maize, soybean or alfalfa) or in for example pupae of the silkworm Bombix mori.

0198Furthermore, the Nanobodies and polypeptides of the invention can also be expressed and/or produced in cell-free expression systems, and suitable examples of such systems will be clear to the skilled person. Some preferred, but non-limiting examples include expression in the wheat germ system; in rabbit reticulocyte lysates; or in the <i>E. coli</i> Zubay system.

0199As mentioned above, one of the advantages of the use of Nanobodies is that the polypeptides based thereon can be prepared through expression in a suitable bacterial system, and suitable bacterial expression systems, vectors, host cells, regulatory elements, etc., will be clear to the skilled person, for example from the references cited above. It should however be noted that the invention in its broadest sense is not limited to expression in bacterial systems.

0200Preferably, in the invention, an (in vivo or in vitro) expression system, such as a bacterial expression system, is used that provides the polypeptides of the invention in a form that is suitable for pharmaceutical use, and such expression systems will again be clear to the skilled person. As also will be clear to the skilled person, Polypeptides of the invention suitable for pharmaceutical use can be prepared using techniques for peptide synthesis.

0201For production on industrial scale, preferred heterologous hosts for the (industrial) production of Nanobodies or Nanobody-containing protein therapeutics include strains of E. <i>coli, Pichia pastoris, S. cerevisiae</i> that are suitable for large scale expression/production/fermentation, and in particular for large scale pharmaceutical expression/production/fermentation. Suitable examples of such strains will be clear to the skilled person. Such strains and production/expression systems are also made available by companies such as Biovitrum (Uppsala, Sweden).

0202Alternatively, mammalian cell lines, in particular Chinese hamster ovary (CHO) cells, can be used for large scale expression/production/fermentation, and in particular for large scale pharmaceutical expression/production/fermentation. Again, such expression/production systems are also made available by some of the companies mentioned above.

0203The choice of the specific expression system would depend in part on the requirement for certain post-translational modifications, more specifically glycosylation. The production of a Nanobody-containing recombinant protein for which glycosylation is desired or required would necessitate the use of mammalian expression hosts that have the ability to glycosylate the expressed protein. In this respect, it will be clear to the skilled person that the glycosylation pattern obtained (i.e. the kind, number and position of residues attached) will depend on the cell or cell line that is used for the expression. Preferably, either a human cell or cell line is used (i.e. leading to a protein that essentially has a human glycosylation pattern) or another mammalian cell line is used that can provide a glycosylation pattern that is essentially and/or functionally the same as human glycosylation or at least mimics human glycosylation. Generally, prokaryotic hosts such as E. coli do not have the ability to glycosylate proteins, and the use of lower eukaryotes such as yeast are usually leads to a glycosylation pattern that differs from human glycosylation. Nevertheless, it should be understood that all the foregoing host cells and expression systems can be used in the invention, depending on the desired Nanobody or protein to be obtained.

0204Thus, according to one non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is glycosylated. According to another non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is non-glycosylated.

0205According to one preferred, but non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is produced in a bacterial cell, in particular a bacterial cell suitable for large scale pharmaceutical production, such as cells of the strains mentioned above.

0206According to another preferred, but non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is produced in a yeast cell, in particular a yeast cell suitable for large scale pharmaceutical production, such as cells of the species mentioned above.

0207According to yet another preferred, but non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is produced in a mammalian cell, in particular in a human cell or in a cell of a human cell line, and more in particular in a human cell or in a cell of a human cell line that is suitable for large scale pharmaceutical production, such as the cell lines mentioned hereinabove.

0208When expression in a host cell is used to produce the Nanobodies and the proteins of the invention, the Nanobodies and proteins of the invention can be produced either intracellullarly (e.g. in the cytosol, in the periplasma or in inclusion bodies) and then isolated from the host cells and optionally further purified; or can be produced extracellularly (e.g. in the medium in which the host cells are cultured) and then isolated from the culture medium and optionally further purified. When eukaryotic hosts cells are used, extracellular production is usually preferred since this considerably facilitates the further isolation and downstream processing of the Nanobodies and proteins obtained. Bacterial cells such as the strains of E. coli mentioned above normally do not secrete proteins extracellularly, except for a few classes of proteins such as toxins and hemolysin, and secretory production in E. coli refers to the translocation of proteins across the inner membrane to the periplasmic space. Periplasmic production provides several advantages over cytosolic production. For example, the N-terminal amino acid sequence of the secreted product can be identical to the natural gene product after cleavage of the secretion signal sequence by a specific signal peptidase. Also, there appears to be much less protease activity in the periplasm than in the cytoplasm. In addition, protein purification is simpler due to fewer contaminating proteins in the periplasm. Another advantage is that correct disulfide bonds may form because the periplasm provides a more oxidative environment than the cytoplasm. Proteins overexpressed in E. coli are often found in insoluble aggregates, so-called inclusion bodies. These inclusion bodies may be located in the cytosol or in the periplasm; the recovery of biologically active proteins from these inclusion bodies requires a denaturation/refolding process. Many recombinant proteins, including therapeutic proteins, are recovered from inclusion bodies. Alternatively, as will be clear to the skilled person, recombinant strains of bacteria that have been genetically modified so as to secrete a desired protein, and in particular a Nanobody or a polypeptide of the invention, can be used.

0209Thus, according to one non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is a Nanobody or polypeptide that has been produced intracellularly and that has been isolated from the host cell, and in particular from a bacterial cell or from an inclusion body in a bacterial cell. According to another non-limiting embodiment of the invention, the Nanobody or polypeptide of the invention is a Nanobody or polypeptide that has been produced extracellularly, and that has been isolated from the medium in which the host cell is cultivated.

0210Some preferred, but non-limiting promoters for use with these host cells include, <ul id="ul0074" list-style="dash" compact="compact"><li>for expression in E. coli: lac promoter (and derivatives thereof such as the lacUV5 promoter); arabinose promoter; left- (PL) and rightward (PR) promoter of phage lambda; promoter of the trp operon; hybrid lac/trp promoters (tac and trc); T7-promoter (more specifically that of T7-phage gene 10) and other T-phage promoters; promoter of the Tn10 tetracycline resistance gene; engineered variants of the above promoters that include one or more copies of an extraneous regulatory operator sequence;</li><li>for expression in S. cerevisiae: constitutive: ADH1 (alcohol dehydrogenase 1), ENO (enolase), CYC1 (cytochrome c iso-1), GAPDH (glyceraldehydes-3-phosphate dehydrogenase); PGK1 (phosphoglycerate kinase), PYK1 (pyruvate kinase); regulated: GAL1,10,7 (galactose metabolic enzymes), ADH2 (alcohol dehydrogenase 2), PHO5 (acid phosphatase), CUP1 (copper metallothionein); heterologous: CaMV (cauliflower mosaic virus 35S promoter);</li><li>for expression in Pichia pastoris: the AOX1 promoter (alcohol oxidase I)</li><li>for expression in mammalian cells: human cytomegalovirus (hCMV) immediate early enhancer/promoter; human cytomegalovirus (hCMV) immediate early promoter variant that contains two tetracycline operator sequences such that the promoter can be regulated by the Tet repressor; Herpes Simplex Virus thymidine kinase (TK) promoter; Rous Sarcoma Virus long terminal repeat (RSV LTR) enhancer/promoter, elongation factor 1α (hEF-1α) promoter from human, chimpanzee, mouse or rat; the SV40 early promoter; HIV-1 long terminal repeat promoter; β-actin promoter;</li></ul> Some preferred, but non-limiting vectors for use with these host cells include: <ul id="ul0075" list-style="dash" compact="compact"><li>vectors for expression in mammalian cells: pMAMneo (Clontech), pcDNA3 (Invitrogen), pMClneo (Stratagene), pSG5 (Stratagene), EBO-pSV2-neo (ATCC 37593), pBPV-1 (8-2) (ATCC 37110), pdBPV-MMTneo (342-12) (ATCC 37224), pRSVgpt (ATCC37199), pRSVneo (ATCC37198), pSV2-dhfr (ATCC 37146), pUCTag (ATCC 37460) and 1ZD35 (ATCC 37565), as well as viral-based expression systems, such as those based on adenovirus;</li><li>vectors for expression in bacterials cells: pET vectors (Novagen) and pQE vectors (Qiagen);</li><li>vectors for expression in yeast or other fungal cells: pYES2 (Invitrogen) and Pichia expression vectors (Invitrogen);</li><li>vectors for expression in insect cells: pBlueBacII (Invitrogen) and other baculovirus vectors</li><li>vectors for expression in plants or plant cells: for example vectors based on cauliflower mosaic virus or tobacco mosaic virus, suitable strains of Agrobacterium, or Ti-plasmid based vectors.</li></ul> Some preferred, but non-limiting secretory sequences for use with these host cells include: <ul id="ul0076" list-style="dash" compact="compact"><li>for use in bacterial cells such as E. coli: PelB, Bla, OmpA, OmpC, OmpF, OmpT, StII, PhoA, PhoE, MalE, Lpp, LamB, and the like; TAT signal peptide, hemolysin C-terminal secretion signal</li><li>for use in yeast: α-mating factor prepro-sequence, phosphatase (pho1), invertase (Suc), etc.;</li><li>for use in mammalian cells: indigenous signal in case the target protein is of eukaryotic origin; murine Ig κ-chain V-J2-C signal peptide; etc.</li></ul>

0211Suitable techniques for transforming a host or host cell of the invention will be clear to the skilled person and may depend on the intended host cell/host organism and the genetic construct to be used. Reference is again made to the handbooks and patent applications mentioned above.

0212After transformation, a step for detecting and selecting those host cells or host organisms that have been succesfully transformed with the nucleotide sequence/genetic construct of the invention may be performed. This may for instance be a selection step based on a selectable marker present in the genetic construct of the invention or a step involving the detection of the amino acid sequence of the invention, e.g. using specific antibodies.

0213The transformed host cell (which may be in the form or a stable cell line) or host organisms (which may be in the form of a stable mutant line or strain) form further aspects of the present invention.

0214Preferably, these host cells or host organisms are such that they express, or are (at least) capable of expressing (e.g. under suitable conditions), an amino acid sequence of the invention (and in case of a host organism: in at least one cell, part, tissue or organ thereof). The invention also includes further generations, progeny and/or offspring of the host cell or host organism of the invention, that may for instance be obtained by cell division or by sexual or asexual reproduction.

0215To produce/obtain expression of the amino acid sequences of the invention, the transformed host cell or transformed host organism may generally be kept, maintained and/or cultured under conditions such that the (desired) amino acid sequence of the invention is expressed/produced. Suitable conditions will be clear to the skilled person and will usually depend upon the host cell/host organism used, as well as on the regulatory elements that control the expression of the (relevant) nucleotide sequence of the invention. Again, reference is made to the handbooks and patent applications mentioned above in the paragraphs on the genetic constructs of the invention.

0216Generally, suitable conditions may include the use of a suitable medium, the presence of a suitable source of food and/or suitable nutrients, the use of a suitable temperature, and optionally the presence of a suitable inducing factor or compound (e.g. when the nucleotide sequences of the invention are under the control of an inducible promoter); all of which may be selected by the skilled person. Again, under such conditions, the amino acid sequences of the invention may be expressed in a constitutive manner, in a transient manner, or only when suitably induced.

0217It will also be clear to the skilled person that the amino acid sequence of the invention may (first) be generated in an immature form (as mentioned above), which may then be subjected to post-translational modification, depending on the host cell/host organism used. Also, the amino acid sequence of the invention may be glycosylated, again depending on the host cell/host organism used.

0218The amino acid sequence of the invention may then be isolated from the host cell/host organism and/or from the medium in which said host cell or host organism was cultivated, using protein isolation and/or purification techniques known per se, such as (preparative) chromatography and/or electrophoresis techniques, differential precipitation techniques, affinity techniques (e.g. using a specific, cleavable amino acid sequence fused with the amino acid sequence of the invention) and/or preparative immunological techniques (i.e. using antibodies against the amino acid sequence to be isolated).

0219Generally, for pharmaceutical use, the polypeptides of the invention may be formulated as a pharmaceutical preparation comprising at least one polypeptide of the invention and at least one pharmaceutically acceptable carrier, diluent or excipient and/or adjuvant, and optionally one or more further pharmaceutically active polypeptides and/or compounds. By means of non-limiting examples, such a formulation may be in a form suitable for oral administration, for parenteral administration (such as by intravenous, intramuscular or subcutaneous injection or intravenous infusion), for topical administration, for administration by inhalation, by a skin patch, by an implant, by a suppository, etc.. Such suitable administration forms - which may be solid, semi-solid or liquid, depending on the manner of administration - as well as methods and carriers for use in the preparation thereof, will be clear to the skilled person, and are further described hereinbelow.

0220Thus, in a further aspect, the invention relates to a pharmaceutical composition that contains at least one Nanobody of the invention or at least one polypeptide of the invention and at least one suitable carrier (i.e. a carrier suitable for veterinary use), and optionally one or more further active substances.

0221One embodiment of the present invention is a polypeptide construct comprising: at least one Nanobody of the invention, i.e. directed against any of vWF, vWF A1 domain, A1 domain of activated vWF, vWF A3 domain.

0222Another embodiment of the present invention is a polypeptide construct as described above, wherein the Nanobody of the invention directed against the A1 domain of activated vWF specifically recognizes the activated vWF conformation at the site of thrombus formation but does not bind to circulating unactivated forms of vWF.

0223The Nanobodies of the invention may also be directed against a fragment of vWF, vWF A1 domain, A1 domain of activated vWF, vWF A3 domain, such as a fragment capable of eliciting an immune response. A target is also a fragment of vWF, vWF A1 domain, A1 domain of activated vWF, vWF A3 domain, capable of binding to a Nanobody of the invention raised against the 'parent' full length target.

0224A fragment as used herein refers to less than 100% of the sequence (e.g., 99%, 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, 10% etc.), but comprising 5, 6, 7, 8, 9, 10, 12, 13,14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or more amino acids. A fragment is of sufficient length such that the interaction of interest is maintained with affinity of 1 x 10-6 M or better.

0225A fragment as used herein also refers to optional insertions, deletions and substitutions of one or more amino acids which do not substantially alter the ability of the target to bind to a Nanobody of the invention raised against the wild-type target. The number of amino acid insertions deletions or substitutions is preferably up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69 or 70 amino acids.

0226A Nanobody of the invention directed against a target generally means Nanobody of the invention that it is capable of binding to its target with an affinity of better than 10^-6 M.

0227Another embodiment of the present invention is a polypeptide construct as described above wherein at least one Nanobody of the invention is a humanised sequence.

0228Another embodiment of the present invention is a polypeptide construct as described above wherein at least one Nanobody of the invention is a Camelidae V_HH antibody.

0229Another embodiment of the present invention is a polypeptide construct as described above, wherein said Nanobody of the invention is an homologous sequence, a functional portion, or a functional portion of an homologous sequence of the full length Nanobody of the invention.

0230Another embodiment of the present invention is a polypeptide construct as described above, wherein said polypeptide construct is a homologous sequence of said polypeptide construct, a functional portion thereof, of an homologous sequence of a functional portion thereof.

0231Another embodiment of the present invention is a polypeptide construct as described above, further comprising at least one Nanobody of the invention directed against one or more serum proteins, in particular one or more human serum proteins.

0232Another embodiment of the present invention is a polypeptide construct as described above wherein said at least one (human) serum protein is any of (human) serum albumin, (human) serum immunoglobulins, (human) thyroxine-binding protein, (human) transferrine, or (human) fibrinogen or a fragment thereof.

0233According to a specific, but non-limiting aspect of the invention, the polypeptides of the invention contain, besides the one or more Nanobodies of the invention, at least one Nanobody against human serum albumin. Although these Nanobodies against human serum albumin may be as generally described in <patcit id="pcit0096" dnum="WO4062551A"><text>WO4/062551</text></patcit> or in the further references cited therein, according to a particularly preferred, but non-limiting embodiment, said Nanobody against human serum albumin consists of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: i) CDR1 is an amino acid sequence chosen from the group consisting of: <tables id="tabl0027" num="0027"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SFGMS</entry><entry>[SEQ ID NO: 44]</entry></row><row><entry>LNLMG</entry><entry>[SEQ ID NO: 45]</entry></row><row><entry>INLLG</entry><entry>[SEQ ID NO: 46]</entry></row><row><entry>NYWMY;</entry><entry>[SEQ ID NO: 47]</entry></row></tbody></tgroup></table></tables> and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0076" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> and in which: ii) CDR2 is an amino acid sequence chosen from the group consisting of: <tables id="tabl0028" num="0028"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="42mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>SISGSGSDTLYADSVKG</entry><entry>[SEQ ID NO: 48]</entry></row><row><entry>TITVGDSTNYADSVKG</entry><entry>[SEQ ID NO: 49]</entry></row><row><entry>TITVGDSTSYADSVKG</entry><entry>[SEQ ID NO: 50]</entry></row><row><entry>SINGRGDDTRYADSVKG</entry><entry>[SEQ ID NO: 51]</entry></row><row><entry>AISADSSTKNYADSVKG</entry><entry>[SEQ ID NO: 52]</entry></row><row><entry>AISADSSDKRYADSVKG</entry><entry>[SEQ ID NO: 53]</entry></row><row><entry>RISTGGGYSYYADSVKG</entry><entry>[SEQ ID NO: 54]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0077" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0078" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> and in which: iii) CDR3 is an amino acid sequence chosen from the group consisting of: DREAQVDTLDFDY [SEQ ID NO: 55] or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0079" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0080" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> or from the group consisting of: <tables id="tabl0029" num="0029"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="24mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>GGSLSR</entry><entry>[SEQ ID NO: 56]</entry></row><row><entry>RRTWHSEL</entry><entry>[SEQ ID NO: 57]</entry></row><row><entry>GRSVSRS</entry><entry>[SEQ ID NO: 58]</entry></row><row><entry>GRGSP</entry><entry>[SEQ ID NO: 59]</entry></row></tbody></tgroup></table></tables> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0081" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences.</li></ol>

0234In another aspect, the invention relates to a Nanobody against vWF, which consist of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), which is chosen from the group consisting of Nanobodies with the one of the following combinations of CDR1, CDR2 and CDR3, respectively: <ul id="ul0077" list-style="dash" compact="compact"><li><b>CDR1:</b> SFGMS; <b>CDR2:</b> SISGSGSDTLYADSVKG; <b>CDR3:</b> GGSLSR;</li><li><b>CDR1:</b> LNLMG; <b>CDR2:</b> TITVGDSTNYADSVKG; <b>CDR3:</b> RRTWHSEL;</li><li><b>CDR1:</b> INLLG; <b>CDR2</b>: TITVGDSTSYADSVKG; <b>CDR3:</b> RRTWHSEL;</li><li><b>CDR1:</b> SFGMS; <b>CDR2</b>: SINGRGDDTRYADSVKG; <b>CDR3:</b> GRSVSRS;</li><li><b>CDR1:</b> SFGMS; <b>CDR2</b>: AISADSSDKRYADSVKG; <b>CDR3:</b> GRGSP;</li><li><b>CDR1:</b> SFGMS; <b>CDR2:</b> AISADSSDKRYADSVKG; <b>CDR3:</b> GRGSP;</li><li><b>CDR1:</b> NYWMY; <b>CDR2</b>: RISTGGGYSYYADSVKG; <b>CDR3:</b> DREAQVDTLDFDY.</li></ul>

0235In the Nanobodies of the invention that comprise the combinations of CDR's mentioned above, each CDR can be replaced by a CDR chosen from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with the mentioned CDR's; in which <ol id="ol0082" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences;</li></ol> and/or chosen from the group consisting of amino acid sequences that have 3, 2 or only 1 (as indicated in the preceding paragraph) "amino acid difference(s)" (as defined herein) with the mentioned CDR(s) one of the above amino acid sequences, in which: <ol id="ol0083" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequences.</li></ol>

0236However, of the Nanobodies of the invention that comprise the combinations of CDR's mentioned above, Nanobodies comprising one or more of the CDR's listed above are particularly preferred; Nanobodies comprising two or more of the CDR's listed above are more particularly preferred; and Nanobodies comprising three of the CDR's listed above are most particularly preferred.

0237In these Nanobodies against human serum albumin, the Framework regions FR1 to FR4 are preferably as defined hereinabove for the Nanobodies of the invention.

0238Particularly preferred Nanobodies against human serum albumin are chosen from the group consisting of SEQ ID NO's: 107-121. These correspond to the Nanobodies against human serum albumin of SEQ ID NO's: 61 to 67, SEQ ID NO's 87 to 89 and SEQ ID NO's 100-104 from applicant's co-pending US provisional application entitled <i>"Improved Nanobodies</i>™ <i>against Tumor Necrosis Factor-alpha"</i> with a filing date of May 18, 2005.

0239More generally, Nanobodies against serum albumin suitable for use in the invention are described in the International application by applicant entitled "serum albumin binding proteins" with an international filing date of May 17, 2006.

0240Another embodiment of the present invention is a nucleic acid encoding a polypeptide construct as described above.

0241Another embodiment of the present invention is a composition comprising a polypeptide construct as described above and at least one thrombolytic agent, for simultaneous, separate or sequential administration to a subject.

0242Another embodiment of the present invention is a composition as described above wherein said thrombolytic agent is any of staphylokinase, tissue plasminogen activator, streptokinase, single chain streptokinase, urokinase and acyl plasminogen streptokinase complex.

0243Another embodiment of the present invention is a polypeptide construct as described above, or a nucleic acid as described above, or a composition as described above for use in the treatment, prevention and/or alleviation of disorders relating to platelet-mediate aggregation or dysfunction thereof.

0244Another embodiment of the present invention is a use of a polypeptide construct as described above, or a nucleic acid as described above, or a composition as described above for the preparation of a medicament for the treatment, prevention and/or alleviation of disorders relating to platelet-mediate aggregation or dysfunction thereof.

0245Another embodiment of the present invention is a polypeptide construct, nucleic acid or composition as described above or a use of a polypeptide construct, nucleic acid or composition as described above wherein said disorders are any arising from transient cerebral ischemic attack, unstable or stable angina, angina pectoris, cerebral infarction, myocardial infarction, peripheral arterial occlusive disease, restenosis, coronary by-pass graft, or coronary artery valve replacement and coronary interventions such angioplasty, stenting, carotid endarterectomy or atherectomy.

0246Another embodiment of the present invention is a polypeptide construct, nucleic acid or composition as described above or a use of a polypeptide construct, nucleic acid or composition as described above wherein said disorders are any of the formation of a non-occlusive thrombus, the formation of an occlusive thrombus, arterial thrombus formation, acute coronary occlusion, restenosis, restenosis after PCTA or stenting, thrombus formation in stenosed arteries, hyperplasia after angioplasty, atherectomy or arterial stenting, occlusive syndrome in a vascular system or lack of patency of diseased arteries.

0247Another embodiment of the present invention is a polypeptide construct, nucleic acid or composition as described above or a use of a polypeptide construct, nucleic acid or composition as described above wherein said disorder is plaque or thrombus formation in high sheer environments.

0248Another embodiment of the present invention is a polypeptide construct, nucleic acid or composition as described above or a use of a polypeptide construct as described above wherein said polypeptide construct is administered intravenously, subcutaneously, orally, sublingually, topically, nasally, vaginally, rectally or by inhalation.

0249Another embodiment of the present invention is a composition comprising a polypeptide construct as described above or a nucleic acid encoding said polypeptide construct, or a composition as described above and a pharmaceutically acceptable vehicle.

0250Another embodiment of the present invention is a method of producing a polypeptide as described above, comprising <ol id="ol0084" compact="compact"><li>(a) culturing host cells comprising nucleic acid capable of encoding a polypeptide as described above under conditions allowing the expression of the polypeptide, and,</li><li>(b) recovering the produced polypeptide from the culture.</li></ol>

0251Another embodiment of the present invention is a method as described above, wherein said host cells are bacterial or yeast.

0252Another embodiment of the present invention is a method for treating invasive medical devices to prevent platelet-mediate aggregation around the site of invasion comprising the step of coating said device with a polypeptide construct as described above.

0253Another embodiment of the present invention is an invasive medical device for circumventing platelet-mediate aggregation around the site of invasion, wherein said device is coated with a polypeptide construct as described above.

0254Another embodiment of the present invention is a method of identifying an agent that modulates platelet-mediated aggregation comprising <ol id="ol0085" compact="compact"><li>(a) contacting a polypeptide construct as described above with a polypeptide corresponding to its target, or a fragment thereof, in the presence and absence of a candidate modulator under conditions permitting binding between said polypeptides, and</li><li>(b) measuring the binding between the polypeptides of step (a), wherein a decrease in binding in the presence of said candidate modulator, relative to the binding in the absence of said candidate modulator identified said candidate modulator as an agent that modulate platelet-mediated aggregation.</li></ol>

0255Another embodiment of the present invention is a kit for screening for agents that modulate platelet-mediated aggregation according to the method as described above.

0256Another embodiment of the present invention is an unknown agent that modulates platelet-mediated aggregation identified according to the method as described above.

0257Another embodiment of the present invention is a method of diagnosing a disease or disorder characterised by dysfunction of platelet-mediated aggregation comprising the steps of: <ol id="ol0086" compact="compact"><li>(a) contacting a sample with a polypeptide construct as described above, and</li><li>(b) detecting binding of said polypeptide construct to said sample, and</li><li>(c) comparing the binding detected in step (b) with a standard, wherein a difference in binding relative to said sample is diagnostic of a disease or disorder characterised by dysfunction of platelet-mediated aggregation.</li></ol>

0258Another embodiment of the present invention is a kit for screening for diagnosing a disease or disorder characterised by dysfunction of platelet-mediated aggregation according to the method as described above.

0259Another embodiment of the present invention is a kit as described above comprising a polypeptide construct as described above.

0260In the polypeptides of the invention, the one or more Nanobodies of the invention which are directed against a target may be of the same sequence. Alternatively they may not all have the same sequence. It is within the scope of the invention that a polypeptide of the invention comprises anti-target Nanobodies of the invention which do not all share the same sequence, but which are directed against the same target, or fragment thereof, one or more antigens thereof.

0261It is another aspect of the invention that the polypeptide of the invention comprises two or more Nanobodies of the invention, wherein any two Nanobodies of the invention are directed against different epitopes/targets, i.e. against any of vWF, vWF A1 domain, A1 domain of activated vWF, vWF A3 domain.

0262Another aspect of the invention is a bispecific polypeptide of the invention comprising a Nanobody of the invention directed against vWF A1 domain, A1 domain of activated vWF, and another Nanobody of the invention directed against vWF A3 domain. Said bispecific polypeptide of the invention inhibits the interaction between vWF and collagen, and the interaction between vWF and platelets.

0263According to an aspect of the present invention a polypeptide of the invention may comprise two or more Nanobodies of the invention which have been joined. The Nanobodies of the invention may be identical in sequence and directed against the same target or antigen. Depending on the number of V_HHs linked, a multivalent V_HH may be bivalent (2 V_HHs), trivalent (3 V_HHs), tetravalent (4 V_HHs) or have a higher valency molecules.

0264The present invention also relates to the finding that a polypeptide of the invention further comprising one or more Nanobodies of the invention each directed against a serum protein of a subject, surprisingly has significantly prolonged half-life in the circulation of said subject compared with the half-life of the anti-target Nanobody of the invention(ies) when not part of said construct. Furthermore, the said constructs were found to exhibit the same favourable properties of V_HHs such as high stability remaining intact in mice, extreme pH resistance, high temperature stability and high target affinity.

0265The serum protein may be any suitable protein found in the serum of subject, or fragment thereof. In one aspect of the invention, the serum protein is serum albumin, serum immunoglobulins, thyroxine-binding protein, transferrin, or fibrinogen. Depending on the intended use such as the required half-life for effective treatment and/or compartimentalisation of the target antigen, the V_HH-partner can be directed to one of the above serum proteins.

0266Such constructs are able to circulate in the subject's serum for several days, reducing the frequency of treatment, the inconvenience to the subject and resulting in a decreased cost of treatment. Furthermore, it is an aspect of the invention that the half-life of the polypeptide of the invention disclosed herein may be controlled by the number of anti-serum protein Nanobodies of the invention present in the construct. A controllable half-life is desirable in several circumstances, for example, in the application of a timed dose of a therapeutic polypeptide of the invention.

0267Another embodiment of the present invention is a polypeptide of the invention as mentioned herein, further comprising a thrombolytic agent.

0268Said thrombolytic agent may be non-covalently or covalently attached to a Nanobody of the invention via covalent or non-covalent means. Such covalent means are described below. Non-covalent means include via a protein interaction such as biotin/strepavidin, or via an immunoconjugate.

0269Alternatively, the thrombolytic agent may be administered simultaneous, separate or sequential in respect of a polypeptide of the invention.

0270Another aspect of the invention is a composition comprising at least one polypeptide of the invention and at least one thrombolytic agent, for simultaneous, separate or sequential administration to a subject.

0271One aspect of the invention is a method for treating autoimmune disease comprising administering to an individual an effective amount of at least one polypeptide of the invention and at least one thrombolytic agent, simultaneously, separately or sequentially.

0272Another aspect of the invention is a kit containing at least one polypeptide of the invention and at least one thrombolytic agent for simultaneous, separate or sequential administration to a subject. It is an aspect of the invention that the kit may be used according to the invention. It is an aspect of the invention that the kit may be used to treat the diseases as cited herein.

0273By simultaneous administration means the polypeptide and thrombolytic agent are administered to a subject at the same time. For example, as a mixture or a composition comprising said components. Examples include, but are not limited to a solution administered intraveneously, a tablet, liquid, topical cream, etc., wherein each preparation comprises the components of interest.

0274By separate administration means polypeptide and thrombolytic agent are administered to a subject at the same time or substantially the same time. The components are present in the kit as separate, unmixed preparations. For example, the polypeptide and thrombolytic agent may be present in the kit as individual tablets. The tablets may be administered to the subject by swallowing both tablets at the same time, or one tablet directly following the other.

0275By sequential administration means the polypeptide and thrombolytic agent are administered to a subject sequentially. The polypeptide and thrombolytic agent are present in the kit as separate, unmixed preparations. There is a time interval between doses. For example, one component might be administered up to 336, 312, 288, 264, 240, 216, 192, 168, 144, 120, 96, 72, 48, 24, 20, 16, 12, 8, 4, 2, 1, or 0.5 hours after the other component.

0276In sequential administration, one component may be administered once, or any number of times and in various doses before and/or after administration of another component. Sequential administration may be combined with simultaneous or sequential administration.

0277The medical uses of the polypeptide of the invention described below, also apply to the composition comprising a polypeptide of the invention and at least one polypeptide thrombolytic agent, for simultaneous, separate or sequential administration to a subject as disclosed here above.

0278Thrombolytic agents according to the invention may include, for example, staphylokinase, tissue plasminogen activator, streptokinase, single chain streptokinase, urokinase and acyl plasminogen streptokinase complex.

0279The Nanobodies of the invention may be joined to form any of the polypeptide of the invention disclosed herein comprising more than one Nanobody of the invention using methods known in the art or any future method. For example, they may be fused by chemical cross-linking by reacting amino acid residues with an organic derivatisation agent such as described by <nplcit id="ncit0122" npl-type="s"><text>Blattler et al, Biochemistry 24,1517-1524</text></nplcit>; <patcit id="pcit0097" dnum="EP294703A"><text>EP294703</text></patcit>. Alternatively, the Nanobody of the invention may be fused genetically at the DNA level i.e. a polynucleotide construct formed which encodes the complete polypeptide of the invention comprising one or more anti-target Nanobodies of the invention and one or more anti-serum protein Nanobodies of the invention. A method for producing bivalent or multivalent V_HH polypeptide of the invention is disclosed in <patcit id="pcit0098" dnum="WO9634103A"><text>PCT patent application WO 96/34103</text></patcit>. One way of joining multiple Nanobodies of the invention is via the genetic route by linking Nanobody of the invention coding sequences either directly or via a peptide linker. For example, the C-terminal end of the first Nanobody of the invention may be linked to the N-terminal end of the next Nanobody of the invention. This linking mode can be extended in order to link additional Nanobodies of the invention for the construction and production of tri-, tetra-, etc. functional constructs.

0280The polypeptide of the invention disclosed herein may be made by the skilled artisan according to methods known in the art or any future method. For example, V_HHs may be obtained using methods known in the art such as by immunising a camel and obtaining hybridoma's therefrom, or by cloning a library of Nanobodies of the invention using molecular biology techniques known in the art and subsequent selection by using phage display.

0281Nanobodies have a unique structure that consists of a single variable domain. V_HH molecules derived from Camelidae antibodies are among the smallest intact antigen-binding domains known (approximately 15 kDa, or 10 times smaller than a conventional IgG) and hence are well suited towards delivery to dense tissues and for accessing the limited space between macromolecules participating in or starting the process of platelet mediated aggregation.

0282Despite the small size of nanobodies, and thus advantages for penetration, it is still surprising that such a small molecule can inhibit interactions between large polymers such as vWF (up to 60 monomers) and collagen and with such a high efficiency. It has been described that only the large multimeric forms of vWF are hemostatically active (<nplcit id="ncit0123" npl-type="s"><text>Furlan, M,. 1996, Ann. Hematol. 72:341-348</text></nplcit>). Binding of multimeric vWF to collagen occurs with ∼100-fold higher affinity than binding of monomeric vWF fragments.

0283The results from the high shear experiments indicate that a lower dose may be administered to patients. Therefore, fewer side effects are expected (such as immunogenicity or bleeding problems).

0284In another embodiment of the present invention, a polypeptide of the invention comprises one or more Nanobodies of the invention directed to the same target, and further comprises one or more Nanobodies of the invention directed to the same target but to a different epitope in the same domain.

0285Another embodiment of the present invention is a polypeptide of the invention wherein the number of Nanobodies of the invention directed to the same target is two or more.

0286In another embodiment of the present invention, a polypeptide of the invention comprises one or more Nanobodies of the invention directed to one domain of the same target, and one or more Nanobodies of the invention directed to the same target but to another domain of the same target. Examples of different domains might be the A1 and A3 domains of vWF

0287It is one non-limiting aspect of the invention that at least one V_HH directed to the A1 domain in a heterospecific polypeptide of the invention recognizes the active conformation of vWF. Such polypeptide of the invention may have superior anti-thrombotic effects compared to the monomeric V_HH's. Perfusion experiment were performed in a flow chamber, to study platelet aggregation under high shear to study the effects of these polypeptide of the invention.

0288The discovery of naturally occurring Nanobodies of the invention in llama, dromedary and camel revealed a new class of therapeutic molecules which combine the advantages of monoclonal antibodies for example specificity, low toxicity with the advantages of small molecules for example tissue penetration and stability. Unfortunately, the development of appropriate therapeutic products based on these proteins has the drawback of being Camelidae derived, and thus not human. Non-human proteins contain amino acid residues that can be immunogenic when injected into a human patient. Although studies have shown that Camelidae-derived V_HH are not immunogenic when injected in mice, replacing Camelidae residues by human residues is preferable. These humanized polypeptides should be substantially non-immunogenic in humans, but retain the affinity and activity of the wild type polypeptide.

0289The result of humanisation is preferably that immunogenicity upon administration in human patients is minor or nonexistent. Humanising a polypeptide, according to the present invention, comprises a step of replacing one or more of the Camelidae amino acids by their human counterpart as found in the human consensus sequence, without that polypeptide losing its typical character, i.e. the humanisation does not significantly affect the antigen binding capacity of the resulting polypeptide.

0290<patcit id="pcit0099" dnum="WO04062551A"><text>WO 04/062551</text></patcit> and the further description herein describe some preferred, but non-limiting examples of amino acid residues of the antibody variable domain (V_HH) which may be modified without diminishing the native affinity of the domain for antigen and while reducing its immunogenicity with respect to a heterologous species; the use of V_HHs having modifications at the identified residues which are useful for administration to heterologous species; and to the V_HH so modified. More specifically, the invention also encompasses the preparation of modified V_HHs, which are modified for administration to humans, the resulting V_HH themselves, and the use of such "humanized" V_HHs in the treatment of diseases in humans.

0291As mentioned in <patcit id="pcit0100" dnum="WO04062551A"><text>WO 04/062551</text></patcit> and in the further description herein, humanization of V_HH polypeptides requires the introduction and mutagenesis of only a limited number of amino acids in a single polypeptide chain without dramatic loss of binding and/or inhibition activity. This is in contrast to humanization of scFv, Fab, (Fab)2 and IgG, which requires the introduction of amino acid changes in two chains, the light and the heavy chain and the preservation of the assembly of both chains.

0292A humanisation technique may be performed by a method comprising the replacement of any of the following residues either alone or in combination: FR1 positions 1, 5, 28 and 30, the hallmark amino acid at position 37, 44, 45 and 47 in FR2, FR3 residues 74, 75, 76, 83, 84, 93 and 94 and positions 103, 104, 108 and 111 in FR4 ; numbering according to the Kabat numbering.

0293The Nanobodies of the invention have a high degree of homology to human germline VH DP-47. Further humanization may also involve the introduction and mutagenesis of a limited amount of amino acids in a single polypeptide chain. This is in contrast to humanization of scFv, Fab, (Fab)2 and IgG, which requires the introduction of amino acid changes in two chains, the light and the heavy chain and the preservation of the assembly of both chains.

0294The polypeptides contain human-like residues in FR2. Humanization may also involve mutagenesis of residues in FR1 at position 1 and 5 which were introduced by the primer used for repertoire cloning and do not occur naturally in the llama sequence. Mutagenesis of those residues did not result in loss of binding and/or inhibition activity. Humanization of FR1 also required mutagenesis of position 28 and 30. Mutagenesis of those residues also did not result in loss of binding and/or inhibition activity.

0295Humanization may also involve mutagenesis of residues in FR3 at position 74, 75, 76, 83, 84, 93, 94. Mutagenesis of those residues did not result in loss of binding and/or inhibition activity.

0296Humanization may also involve mutagenesis of residues in FR4 at position 104, 108 and 111. Mutagenesis of Q108L resulted in lower production level in Escherichia coli. Position 108 is solvent exposed in camelid V_HH, while in human antibodies this position is buried at the VH-VL interface (Spinelli, 1996; Nieba, 1997). In isolated V_Hs position 108 is solvent exposed. The introduction of a non-polar hydrophobic Leu instead of polar uncharged Gin can have a drastic effect on the intrinsic foldability/stability of the molecule.

0297One embodiment of the present invention is a method for humanizing a V_HH comprising the steps of: <ol id="ol0087" compact="compact"><li>(a) replacing of any of the following residues either alone or in combination: <ul id="ul0078" list-style="none" compact="compact"><li>FR1 positions 1, 5, 28 and 30, the hallmark amino acid at position 37, 44, 45 and 47 in FR2,</li><li>FR3 residues 74, 75, 76, 83, 84, 93 and 94 , and positions 103, 104, 108 and 111 in FR4 ; numbering according to the Kabat numbering.</li></ul></li></ol>

0298Examples of such humanized sequences are given below and in the appended sequence listing.

0299The use of antibodies derived from sources such as mouse, sheep, goat, rabbit etc., and humanised derivatives thereof as a treatment for conditions which require a modulation of platelet-associated aggregation, is problematic for several reasons. Traditional antibodies are not stable at room temperature, and have to be refrigerated for preparation and storage, requiring necessary refrigerated laboratory equipment, storage and transport, which contribute towards time and expense. Refrigeration is sometimes not feasible in developing countries. The yields of expression of said Fab molecules are very low and the method of production is very labor intensive. Furthermore, the manufacture or small-scale production of said antibodies is expensive because the mammalian cellular systems necessary for the expression of intact and active antibodies require high levels of support in terms of time and equipment, and yields are very low. Furthermore, traditional antibodies have a binding activity which depends upon pH, and hence are unsuitable for use in environments outside the usual physiological pH range such as, for example, in treating gastric bleeding, gastric surgery. Furthermore, traditional antibodies are unstable at low or high pH and hence are not suitable for oral administration. However, it has been demonstrated that camelid antibodies resist harsh conditions, such as extreme pH, denaturing reagents and high temperatures (<nplcit id="ncit0124" npl-type="s"><text>Ewert S et al, Biochemistry 2002 Mar 19;41(11):3628-36</text></nplcit>), so making them suitable for delivery by oral administration. Furthermore, traditional antibodies have a binding activity which depends upon temperature, and hence are unsuitable for use in assays or kits performed at temperatures outside biologically active-temperature ranges (e.g. 37 ± 20°C).

0300The Nanobodies and polypeptides of the invention not only possess the advantageous characteristics of conventional antibodies, such as low toxicity and high selectivity, but they also exhibit additional properties. They are more soluble, meaning they may be stored and/or administered in higher concentrations compared with conventional antibodies. They are stable at room temperature meaning they may be prepared, stored and/or transported without the use of refrigeration equipment, conveying a cost, time and environmental savings. Other advantageous characteristics as compared to conventional antibodies include short half-life in the circulation which may be modulated according to the invention by, for example, albumin-coupling, a bispecific nanobody with one specificity against albumin and the other against the target, Fc coupling, V_HH coupling (bivalent V_HHs) or by pegylation. A short and controllable half-life is desirable for surgical procedures, for example, which require an inhibition of platelet-mediated aggregation for a limited time period. Also, when bleeding problems occur or other complications, dosage can be lowered immediately. The polypeptides of the present invention also retain binding activity at a pH and temperature outside those of usual physiological ranges, which means they may be useful in situations of extreme pH and temperature which require a modulation of platelet-mediated aggregation, such as in gastric surgery, control of gastric bleeding, assays performed at room temperature etc. The polypeptides of the present invention also exhibit a prolonged stability at extremes of pH, meaning they would be suitable for delivery by oral administration. The polypeptides of the present invention may be cost-effectively produced through fermentation in convenient recombinant host organisms such as Escherichia coli and yeast; unlike conventional antibodies which also require expensive mammalian cell culture facilities, achievable levels of expression are high. Examples of yields of the polypeptides of the present invention are 1 to 10 mg/ml (E. coli) and up to 1g/l (yeast). The polypeptides of the present invention also exhibit high binding affinity for a broad range of different antigen types, and ability to bind to epitopes not recognised by conventional antibodies; for example they display long CDR-based loop structures with the potential to penetrate into cavities and exhibit enzyme function inhibition. Furthermore, since binding often occurs through the CDR3 loop only, it is envisaged that peptides derived from CDR3 could be used therapeutically (<nplcit id="ncit0125" npl-type="s"><text>Desmyter et al., J Biol Chem, 2001, 276: 26285-90</text></nplcit>). The polypeptides of the invention are also able to retain full binding capacity as fusion protein with an enzyme or toxin. Furthermore, it might be expected that the undesirable thrombocytopenia caused by Fc:Fc receptor mediated activation of platelet aggregation and/or F(ab')(2)-mediated crosslinking of platelets which has been observed when using intact IgG or F(ab')(2) therapeutically in vivo (see <nplcit id="ncit0126" npl-type="s"><text>Cauwenberghs N. et al, Arteriosclerosis, Thrombosis and Vascular biology, 2000, 20: 1347</text></nplcit>), will be avoided in the use of V_HH, since V_HH contains no Fc and it is not bivalent. Thus the polypeptides of the invention, homologues or functional portions thereof provide a considerable cost and time saving in the treatment and diagnosis of conditions related to platelet-mediated aggregation, and the patient in need of said polypeptides would encounter fewer of the problems associated with conventional agents.

0301Platelet-mediated aggregation is the process wherein vWF-bound collagen adheres to platelets and/or platelet receptors, ultimately resulting in platelet activation. Platelet activation leads to fibrinogen binding, and finally to platelet aggregation. It is within the scope of the present invention to provide polypeptides which modulate the processes which comprise platelet-mediated aggregation such as vWF-collagen binding, vWF-platelet receptor adhesion, collagen-platelet receptor adhesion, platelet activation, fibrinogen binding and/or platelet aggregation.

0302According to an aspect of the invention a polypeptide of the invention may be a homologous sequence of a full-length polypeptide of the invention. According to another aspect of the invention, a polypeptide of the invention may be a functional portion of a full-length polypeptide of the invention. According to another aspect of the invention, a polypeptide of the invention may be a homologous sequence of a full length polypeptide of the invention. According to another aspect of the invention, a polypeptide of the invention may be a functional portion of a homologous sequence of a full length polypeptide of the invention. According to an aspect of the invention a polypeptide of the invention may comprise a sequence of a polypeptide of the invention.

0303According to an aspect of the invention a Nanobody of the invention used to form a polypeptide of the invention may be a complete Nanobody of the invention (e.g. a V_HH) or a homologous sequence thereof. According to another aspect of the invention, a Nanobody of the invention used to form the polypeptide of the invention may be a functional portion of a complete Nanobody of the invention. According to another aspect of the invention, a Nanobody of the invention used to form the polypeptide of the invention may be a homologous sequence of a complete Nanobody of the invention. According to another aspect of the invention, a Nanobody of the invention used to form the polypeptide of the invention may be a functional portion of a homologous sequence of a complete Nanobody of the invention.

0304According to another aspect of the invention a polypeptide of the invention may be an homologous sequence of the parent sequence. According to another aspect of the invention, a polypeptide of the invention may be a functional portion parent sequence. According to another aspect of the invention, a polypeptide of the invention may be a functional portion of a homologous sequence of the parent sequence.

0305As used herein, an homologous sequence may comprise additions, deletions or substitutions of one or more amino acids, which do not substantially alter the functional characteristics of the polypeptide. The number of amino acid deletions or substitutions is preferably up to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69 or 70 amino acids.

0306A homologous sequence according to the present invention includes polypeptides extended by the addition of amino acids to form human heavy chain antibody or human single domain heavy chain antibody, which do not substantially alter the functional characteristics of the unmodified polypeptide.

0307Where homologous sequence indicates sequence identity, it means a sequence which presents a high sequence identity (more than 70%, 75%, 80%, 85%, 90%, 95% or 98% sequence identity) with the parent sequence, and is preferably characterised by similar properties of the parent sequence, namely affinity, said identity calculated using known methods.

0308Alternatively, an homologous sequence may also be any amino acid sequence resulting from allowed substitutions at any number of positions of the parent sequence according to the formula below: <ul id="ul0079" list-style="none" compact="compact"><li>Ser substituted by Ser, Thr, Gly, and Asn;</li><li>Arg substituted by one of Arg, His, Gin, Lys, and Glu;</li><li>Leu substituted by one of Leu, Ile, Phe, Tyr, Met, and Val;</li><li>Pro substituted by one of Pro, Gly, Ala, and Thr;</li><li>Thr substituted by one of Thr, Pro, Ser, Ala, Gly, His, and Gln;</li><li>Ala substituted by one of Ala, Gly, Thr, and Pro;</li><li>Val substituted by one of Val, Met, Tyr, Phe, Ile, and Leu;</li><li>Gly substituted by one of Gly, Ala, Thr, Pro, and Ser;</li><li>Ile substituted by one of Ile, Met, Tyr, Phe, Val, and Leu;</li><li>Phe substituted by one of Phe, Tip, Met, Tyr, Ile, Val, and Leu;</li><li>Tyr substituted by one of Tyr, Trp, Met, Phe, Ile, Val, and Leu;</li><li>His substituted by one of His, Glu, Lys, Gln, Thr, and Arg;</li><li>Gln substituted by one of Gln, Glu, Lys, Asn, His, Thr, and Arg;</li><li>Asn substituted by one of Asn, Glu, Asp, Gln, and Ser;</li><li>Lys substituted by one of Lys, Glu, Gln, His, and Arg;</li><li>Asp substituted by one of Asp, Glu, and Asn;</li><li>Glu substituted by one of Glu, Asp, Lys, Asn, Gln, His, and Arg;</li><li>Met substituted by one of Met, Phe, Ile, Val, Leu, and Tyr.</li></ul>

0309A homologous according to the present invention may refer to nucleotide sequences of more than 50, 100, 200, 300, 400, 500, 600, 800 or 1000 nucleotides able to hybridize to the reverse-complement of the nucleotide sequence capable of encoding a polypeptide under stringent hybridisation conditions (such as the ones described by <nplcit id="ncit0127" npl-type="b"><text>SAMBROOK et al., Molecular Cloning, Laboratory Manuel, Cold Spring, Harbor Laboratory press, New York</text></nplcit>).

0310As used herein, a functional portion refers to a Nanobody of the invention of sufficient length such that the interaction of interest is maintained with affinity of 1 x 10-6 M or better.

0311Alternatively a functional portion of a Nanobody of the invention comprises a partial deletion of the complete amino acid sequence and still maintains the binding site(s) and protein domain(s) necessary for the binding of and interaction with the target.

0312Alternatively a functional portion of any of Nanobody of the invention is a polypeptide which comprises a partial deletion of the complete amino acid sequence and which still maintains the binding site(s) and protein domain(s) necessary for the inhibition of binding of vWF to collagen.

0313Alternatively a functional portion of any Nanobody of the invention is a polypeptide which comprises a partial deletion of the complete amino acid sequence and which still maintains the binding site(s) and protein domain(s) necessary for the binding of and interaction with the A1 domain of vWF.

0314Alternatively a functional portion of any Nanobody of the invention is a polypeptide which comprises a partial deletion of the complete amino acid sequence and which still maintains the binding site(s) and protein domain(s) necessary for the binding of and interaction with collagen.

0315Alternatively a functional portion comprises a partial deletion of the complete amino acid sequence of a polypeptide and which still maintains the binding site(s) and protein domain(s) necessary for the binding of and interaction with the antigen against which it was raised. It includes, but is not limited to V_HH domains.

0316As used herein, a functional portion as it refers to a polypeptide sequence refers to less than 100% of the sequence (e.g., 99%, 90%, 80%, 70%, 60% 50% etc.), but comprising 5 or more amino acids.

0317A portion as it refers to a nucleotide sequence encoding a polypeptide sequence refers to less than 100% of the sequence (e.g.; 99%, 90%, 80%, 70%, 60% 50% etc.), but comprising 15 or more nucleotides.

0318An aspect of the present invention is the administration of a polypeptide of the invention according to the invention can avoid the need for injection. Conventional antibody-based therapeutics have significant potential as drugs because they have exquisite specificity to their target and a low inherent toxicity, however, they have one important drawback: they are relatively unstable, and are sensitive to breakdown by proteases. This means that conventional antibody drugs cannot be administered orally, sublingually, topically, nasally, vaginally, rectally or by inhalation because they are not resistant to the low pH at these sites, the action of proteases at these sites and in the blood and/or because of their large size. They have to be administered by injection (intravenously, subcutaneously, etc.) to overcome some of these problems. Administration by injection requires specialist training in order to use a hypodermic syringe or needle correctly and safely. It further requires sterile equipment, a liquid formulation of the therapeutic polypeptide, vial packing of said polypeptide in a sterile and stable form and, of the subject, a suitable site for entry of the needle. Furthermore, subjects commonly experience physical and psychological stress prior to and upon receiving an injection.

0319An aspect of the present invention overcomes these problems of the prior art, by providing the polypeptides constructs of the present invention. Said constructs are sufficiently small, resistant and stable to be delivered orally, sublingually, topically, nasally, vaginally, rectally or by inhalation substantial without loss of activity. The polypeptides constructs of the present invention avoid the need for injections, are not only cost/time savings, but are also more convenient and more comfortable for the subject.

0320One embodiment of the present invention is a polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the gastric environment without the substance being inactivated.

0321As known by persons skilled in the art, once in possession of said polypeptide of the invention, formulation technology may be applied to release a maximum amount of polypeptide in the right location (in the stomach, in the colon, etc.). This method of delivery is important for treating, prevent and/or alleviate the symptoms of disorders whose targets are located in the gut system.

0322An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of a disorder susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the gastric environment without being inactivated, by orally administering to a subject a polypeptide of the invention.

0323Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the gastric environment without being inactivated.

0324An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the gut system without said substance being inactivated, by orally administering to a subject a Nanobody or polypeptide of the invention.

0325An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject without the substance being inactivated, by orally administering to a subject a Nanobody or polypeptide of the invention.

0326Another embodiment of the present invention is a Nanobody or polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms or disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the vaginal and/or rectal tract.

0327In a non-limiting example, a formulation according to the invention comprises a Nanobody or polypeptide of the invention, in the form of a gel, cream, suppository, film, or in the form of a sponge or as a vaginal ring that slowly releases the active ingredient over time (such formulations are described in <patcit id="pcit0101" dnum="EP707473A"><text>EP 707473</text></patcit>, <patcit id="pcit0102" dnum="EP684814A"><text>EP 684814</text></patcit>, <patcit id="pcit0103" dnum="US5629001A"><text>US 5629001</text></patcit>).

0328An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the vaginal and/or rectal tract, by vaginally and/or rectally administering to a subject a Nanobody or polypeptide of the invention.

0329Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the vaginal and/or rectal tract.

0330An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the vaginal and/or rectal tract without being said substance being inactivated, by administering to the vaginal and/or rectal tract of a subject a Nanobody or polypeptide of the invention.

0331An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject without said substance being inactivated, by administering to the vaginal and/or rectal tract of a subject a Nanobody or polypeptide of the invention.

0332Another embodiment of the present invention is a Nanobody or polypeptide of the invention, for use in treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the nose, upper respiratory tract and/or lung.

0333In a non-limiting example, a formulation according to the invention, comprises a Nanobody or polypeptide of the invention in the form of a nasal spray (e.g. an aerosol) or inhaler. Since the Nanobody or polypeptide of the invention is small, it can reach its target much more effectively than therapeutic IgG molecules.

0334An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the upper respiratory tract and lung, by administering to a subject a Nanobody or polypeptide of the invention, by inhalation through the mouth or nose.

0335Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the nose, upper respiratory tract and/or lung, without said polypeptide being inactivated,

0336An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the nose, upper respiratory tract and lung without inactivation, by administering to the nose, upper respiratory tract and/or lung of a subject a Nanobody or polypeptide of the invention.

0337An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject without inactivation by administering to the nose, upper respiratory tract and/or lung of a subject a Nanobody or polypeptide of the invention.

0338One embodiment of the present invention is a Nanobody or polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the intestinal mucosa, wherein said disorder increases the permeability of the intestinal mucosa. Because of their small size, a Nanobody or polypeptide of the invention can pass through the intestinal mucosa and reach the bloodstream more efficiently in subjects suffering from disorders which cause an increase in the permeability of the intestinal mucosa.

0339An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the intestinal mucosa, wherein said disorder increases the permeability of the intestinal mucosa, by orally administering to a subject a Nanobody or polypeptide of the invention.

0340This process can be even further enhanced by an additional aspect of the present invention - the use of active transport carriers. In this aspect of the invention, V_HH is fused to a carrier that enhances the transfer through the intestinal wall into the bloodstream. In a non-limiting example, this "carrier" is a second V_HH which is fused to the therapeutic V_HH. Such fusion constructs are made using methods known in the art. The "carrier" V_HH binds specifically to a receptor on the intestinal wall which induces an active transfer through the wall.

0341Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation delivered to the intestinal mucosa, wherein said disorder increases the permeability of the intestinal mucosa.

0342An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the intestinal mucosa without being inactivated, by administering orally to a subject a Nanobody or polypeptide of the invention.

0343An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject without being inactivated, by administering orally to a subject a Nanobody or polypeptide of the invention.

0344This process can be even further enhanced by an additional aspect of the present invention - the use of active transport carriers. In this aspect of the invention, a Nanobody or polypeptide of the invention as described herein is fused to a carrier that enhances the transfer through the intestinal wall into the bloodstream. In a non-limiting example, this "carrier" is a V_HH which is fused to said polypeptide. Such fusion constructs made using methods known in the art. The "carrier" V_HH binds specifically to a receptor on the intestinal wall which induces an active transfer through the wall.

0345One embodiment of the present invention is a Nanobody or polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the tissues beneath the tongue effectively. A formulation of said Nanobody or polypeptide of the invention, for example, a tablet, spray, drop is placed under the tongue and adsorbed through the mucus membranes into the capillary network under the tongue.

0346An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the tissues beneath the tongue effectively, by sublingually administering to a subject a Nanobody or polypeptide of the invention.

0347Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able to pass through the tissues beneath the tongue.

0348An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the tissues beneath the tongue without being inactivated, by administering sublingually to a subject a Nanobody or polypeptide of the invention.

0349An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject without being inactivated, by administering orally to a subject a Nanobody or polypeptide of the invention.

0350One embodiment of the present invention is a Nanobody or polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the skin effectively.

0351A formulation of said Nanobody or polypeptide of the invention, for example, a cream, film, spray, drop, patch, is placed on the skin and passes through.

0352An aspect of the invention is a method for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the skin effectively, by topically administering to a subject a Nanobody or polypeptide of the invention.

0353Another embodiment of the present invention is a use of a Nanobody or polypeptide of the invention for the preparation of a medicament for treating, preventing and/or alleviating the symptoms of disorders susceptible to modulation by a substance that controls platelet mediated aggregation which is able pass through the skin effectively.

0354An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the skin without being inactivated, by administering topically to a subject a Nanobody or polypeptide of the invention.

0355An aspect of the invention is a method for delivering a substance that controls platelet mediated aggregation to the bloodstream of a subject, by administering topically to a subject a Nanobody or polypeptide of the invention.

0356In another embodiment of the present invention, a Nanobody or polypeptide of the invention further comprises a carrier Nanobody of the invention (e.g. V_HH) which acts as an active transport carrier for transport of said Nanobody or polypeptide of the invention via the lung lumen to the blood.

0357A Nanobody or polypeptide of the invention further comprising a carrier that binds specifically to a receptor present on the mucosal surface (bronchial epithelial cells) resulting in the active transport of the polypeptide from the lung lumen to the blood. The carrier Nanobody of the invention may be fused to the Nanobody or polypeptide of the invention. Such fusion constructs made using methods known in the art and are describe herein. The "carrier" Nanobody of the invention binds specifically to a receptor on the mucosal surface which induces an active transfer through the surface.

0358Another aspect of the present invention is a method to determine which Nanobodies of the invention (e.g. V_HHs) are actively transported into the bloodstream upon nasal administration. Similarly, a naïve or immune V_HH phage library can be administered nasally, and after different time points after administration, blood or organs can be isolated to rescue phages that have been actively transported to the bloodstream. A non-limiting example of a receptor for active transport from the lung lumen to the bloodstream is the Fc receptor N (FcRn). One aspect of the invention includes the V_HH molecules identified by the method. Such V_HH can then be used as a carrier V_HH for the delivery of a therapeutic V_HH to the corresponding target in the bloodstream upon nasal administration.

0359One embodiment of the present invention is a Nanobody or polypeptide of the invention for use in treating, preventing and/or alleviating the symptoms of disorders relating to platelet-mediated aggregation or dysfunction thereof. Said disorders include ,thrombotic thrombocytopenic purpura (TTP), transient cerebral ischemic attack, unstable or stable angina pectoris, cerebral infarction, myocardial infarction, peripheral arterial occlusive disease, restenosis. Said disorders further include those arising from coronary by-pass graft, coronary artery valve replacement and coronary interventions such angioplasty, stenting, or atherectomy.

0360Other disorders are any of the formation of a non-occlusive thrombus, the formation of an occlusive thrombus, arterial thrombus formation, acute coronary occlusion, restenosis, restenosis after PCTA or stenting, thrombus formation in stenosed arteries, hyperplasia after angioplasty, atherectomy or arterial stenting, occlusive syndrome in a vascular system or lack of patency of diseased arteries.

0361One aspect of the invention is a Nanobody or polypeptide of the invention for use in the treatment, prevention and/or alleviation of disorders or conditions relating to platelet-mediated aggregation or dysfunction thereof, wherein said Nanobody or polypeptide of the invention is administered intravenously, subcutaneously, orally, sublingually, topically, nasally, vaginally, rectally or by inhalation.

0362Another aspect of the invention is the use of a Nanobody or polypeptide of the invention for the preparation of a medicament for the treatment, prevention and/or alleviation of disorders or conditions relating to platelet-mediated aggregation or dysfunction thereof, wherein said Nanobody or polypeptide of the invention is administered intravenously, subcutaneously, orally, sublingually, topically, nasally, vaginally, rectally or by inhalation.

0363Another aspect of the invention is a method of treating, preventing and/or alleviating disorders or conditions relating to relating to platelet-mediated aggregation or dysfunction thereof, comprising administering to a subject a Nanobody or polypeptide of the invention, wherein said heterospecific Nanobody or polypeptide of the invention is administered intravenously, subcutaneously, orally, sublingually, topically, nasally, vaginally, rectally or by inhalation.

0364Another aspect of the invention is a Nanobody or polypeptide of the invention for use in the treatment, prevention and/or alleviation of disorders or conditions relating to platelet-mediated aggregation or dysfunction thereof.

0365Another aspect of the invention is a use of a polypeptide of the invention for the preparation of a medicament for the treatment, prevention and/or alleviation of disorders or conditions relating to platelet-mediated aggregation or dysfunction thereof.

0366One can use a Nanobody or polypeptide of the invention of the present invention in order to screen for agents that modulate the binding of the polypeptide to a vWF. When identified in an assay that measures binding or said polypeptide displacement alone, agents will have to be subjected to functional testing to determine whether they act as modulators of platelet-mediated aggregation. Some examples of suitable screening methods are discussed in <patcit id="pcit0104" dnum="WO04062551A"><text>WO 04/062551</text></patcit>. Of course, these methods can easily be applied to screening for candidate modulators which alter the binding between the Nanobody or polypeptide of the invention disclosed herein and vWF.

0367A cell that is useful according to the invention is preferably selected from the group consisting of bacterial cells such as, for example, <i>E. coli,</i> yeast cells such as, for example, S. <i>cerevisiae, P. pastoris,</i> insect cells or mammalian cells, e.g. as mentioned above.

0368A cell that is useful according to the invention can be any cell into which a nucleic acid sequence encoding a Nanobody or polypeptide of the invention can be or has been introduced such that the polypeptide is expressed at natural levels or above natural levels, as defined herein. Preferably a polypeptide of the invention that is expressed in a cell exhibits normal or near normal pharmacology, as defined herein.

0369According to a preferred embodiment of the present invention, a cell is selected from the group consisting of COS7-cells, a CHO cell, a LM (TK-) cell, a NIH-3T3 cell, HEK-293 cell, K-562 cell or a 1321N1 astrocytoma cell but also other transferable cell lines.

0370In general, "therapeutically effective amount", "therapeutically effective dose" and "effective amount" means the amount needed to achieve the desired result or results (treating or preventing platelet aggregation). One of ordinary skill in the art will recognize that the potency and, therefore, an "effective amount" can vary for the various Nanobodies or polypeptides that inhibit platelet-mediated aggregation used in the invention. One skilled in the art can readily assess the potency of the Nanobody or polypeptide.

0371By "pharmaceutically acceptable" is meant a material that is not biologically or otherwise undesirable, i.e., the material may be administered to an individual along with the Nanobody or polypeptide without causing any undesirable biological effects or interacting in a deleterious manner with any of the other components of the pharmaceutical composition in which it is contained.

0372The invention disclosed herein is useful for treating or preventing a condition of platelet-mediated aggregation, in a subject and comprising administering a pharmaceutically effective amount of a Nanobody or polypeptide or composition that inhibits BTK and that inhibits platelet-mediated aggregation.

0373The invention disclosed herein is useful for treating or preventing the first steps of thrombus formation, in a subject and comprising administering a pharmaceutically effective amount of a Nanobody or polypeptide or composition according to the invention.

0374The invention disclosed herein is useful for treating or preventing restenosis, in a subject and comprising administering a pharmaceutically effective amount of a Nanobody or polypeptide or composition according to the invention.

0375One aspect of the present invention is the use of Nanobodies or polypeptides of the invention for treating or preventing a condition of platelet-mediated aggregation, in a subject and comprising administering a pharmaceutically effective amount of a Nanobody or polypeptide in combination with another, such as, for example, aspirin.

0376One aspect of the present invention is the use of Nanobodies or polypeptides of the invention for treating or preventing a condition of platelet-mediated aggregation, in a subject and comprising administering a pharmaceutically effective amount of a Nanobody or polypeptide in combination with another, such as, for example, a thrombolytic agent.

0377Another aspect of the present invention is a use of a Nanobody or polypeptide of the invention for treating or preventing plaque or thrombus in an individual. Said plaque or thrombus formation may be under conditions of high sheer. In both thrombosis and reocclusion, the reversible adhesion or tethering of the platelets at high shear rate is followed by a firm adhesion through the collagen receptor on platelets resulting in platelet activation; the tethering of platelets by vWF to collagen exposed in the damaged vessel wall is especially important under high shear conditions. The inventors have found that Nanobody or polypeptide of the invention of the present invention unexpected performed well under high sheer conditions.

0378The present invention is not limited to the administration of formulations comprising a single Nanobody or polypeptide of the invention. It is within the scope of the invention to provide combination treatments wherein a formulation is administered to a patient in need thereof that comprises more than one Nanobody or polypeptide of the invention.

0379Conditions of platelet-mediated aggregation include, but are not limited to, unstable angina, stable angina, angina pectoris, embolus formation, deep vain thrombosis, hemolytic uremic syndrome, hemolytic anemia, acute renal failure, thrombolytic complications, thrombotic thrombocytopenic purpura, disseminated intravascular comgelopathy, thrombosis, coronary heart disease, thromboembolic complications, myocardial infarction, restenosis, and atrial thrombosis formation in atrial fibrillation, chronic unstable angina, transient ischemic attacks and strokes, peripheral vascular disease, arterial thrombosis, pre-eclampsia, embolism, restenosis and/or thrombosis following angioplasty, carotid endarterectomy, anastomosis of vascular grafts, and chronic exposure to cardiovascular devices. Such conditions may also result from thromboembolism and reocculsion during and after thrombolytic therapy, after angioplasty, and after coronary artery bypass.

0380It is well known in the art how to determine the inhibition of platelet-mediated aggregation using the standard tests described herein, or using other similar tests. Preferably, the method would result in at least a 10% reduction in platelet-mediated aggregation, including, for example, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, or any amount in between, more preferably by 90%.

0381Similarly, the method would result in at least a 10% reduction in intracellular calcium mobilisation including, for example, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%. Similarly, the method would result in at least a 10% reduction in the level of phosphorylated PLCg 2 including, for example, 15%, 20%, 25%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%.

0382The reduction can be measured, for example, by comparing the optical impedence in a chronology platelet aggregometer. Any other known measurement method may also be used. For example, (1) upon collagen stimulation, the level of collagen-induced intracellular calcium mobilization increases over time and so the measurement may include measuring the level of collagen-induced intracellular calcium or (2) upon collagen stimulation, the level of phosphorylated PLCg 2 increases over time and so the measurement may include measuring the level of phosphorylated PLCg 2.

0383The cells can be contacted in vitro, for example, by adding a Nanobody or polypeptide of the invention to the culture medium (by continuous infusion, by bolus delivery, or by changing the medium to a medium that contains the Nanobody or polypeptide) or by adding the Nanobody or polypeptide to the extracellular fluid in vivo (by local delivery, systemic delivery, inhalation, intravenous injection, bolus delivery, or continuous infusion). The duration of "contact" with a cell or population of cells is determined by the time the Nanobody or polypeptide is present at physiologically effective levels or at presumed physiologically effective levels in the medium or extracellular fluid bathing the cell or cells. Preferably, the duration of contact is 1-96 hours, and more preferably, for 24 hours, but such time would vary based on the half life of the Nanobody or polypeptide and could be optimized by one skilled in the art using routine experimentation.

0384The Nanobody or polypeptide useful in the present invention can be formulated as pharmaceutical compositions and administered to a mammalian host, such as a human patient or a domestic animal in a variety of forms adapted to the chosen route of administration, i.e., orally or parenterally, by intra-nasally by inhalation, intravenous, intramuscular, topical or subcutaneous routes.

0385The Nanobody or polypeptide of the present invention can also be administered using gene therapy methods of delivery. See, e.g., <patcit id="pcit0105" dnum="US5399346A"><text>U.S. Patent No. 5,399,346</text></patcit>, which is incorporated by reference in its entirety. Using a gene therapy method of delivery, primary cells transfected with the gene for the Nanobody or polypeptide of the present invention can additionally be transfected with tissue specific promoters to target specific organs, tissue, grafts, tumors, or cells.

0386Thus, the present Nanobody or polypeptide may be systemically administered, e.g., orally, in combination with a pharmaceutically acceptable vehicle such as an inert diluent or an assimilable edible carrier. They may be enclosed in hard or soft shell gelatin capsules, may be compressed into tablets, or may be incorporated directly with the food of the patient's diet. For oral therapeutic administration, the Nanobody or polypeptide may be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations should contain at least 0.1% of the Nanobody or polypeptide. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 to about 60% of the weight of a given unit dosage form. The amount of the Nanobody or polypeptide in such therapeutically useful compositions is such that an effective dosage level will be obtained.

0387The tablets, troches, pills, capsules, and the like may also contain the following: binders such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, fructose, lactose or aspartame or a flavoring agent such as peppermint, oil of wintergreen, or cherry flavoring may be added. When the unit dosage form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier, such as a vegetable oil or a polyethylene glycol. Various other materials may be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or capsules may be coated with gelatin, wax, shellac or sugar and the like. A syrup or elixir may contain the Nanobody or polypeptide, sucrose or fructose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring such as cherry or orange flavor. Of course, any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed. In addition, the Nanobody or polypeptide may be incorporated into sustained-release preparations and devices.

0388The Nanobody or polypeptide may also be administered intravenously or intraperitoneally by infusion or injection. Solutions of the Nanobody or polypeptide can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

0389The pharmaceutical dosage forms suitable for injection or infusion can include sterile aqueous solutions or dispersions or sterile powders comprising the active ingredient which are adapted for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes. In all cases, the ultimate dosage form must be sterile, fluid and stable under the conditions of manufacture and storage. The liquid carrier or vehicle can be a solvent or liquid dispersion medium comprising, for example, water, ethanol, a polyol (for example, glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, nontoxic glyceryl esters, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions or by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, buffers or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

0390Sterile injectable solutions are prepared by incorporating the Nanobody or polypeptide in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filter sterilization. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and the freeze drying techniques, which yield a powder of the active ingredient plus any additional desired ingredient present in the previously sterile-filtered solutions.

0391For topical administration, the present Nanobody or polypeptide may be applied in pure form, i.e., when they are liquids. However, it will generally be desirable to administer them to the skin as compositions or formulations, in combination with a dermatologically acceptable carrier, which may be a solid or a liquid.

0392Useful solid carriers include finely divided solids such as talc, clay, microcrystalline cellulose, silica, alumina and the like. Useful liquid carriers include water, hydroxyalkyls or glycols or water-alcohol/glycol blends, in which the present Nanobody or polypeptide can be dissolved or dispersed at effective levels, optionally with the aid of non-toxic surfactants. Adjuvants such as fragrances and additional antimicrobial agents can be added to optimize the properties for a given use. The resultant liquid compositions can be applied from absorbent pads, used to impregnate bandages and other dressings, or sprayed onto the affected area using pump-type or aerosol sprayers.

0393Thickeners such as synthetic polymers, fatty acids, fatty acid salts and esters, fatty alcohols, modified celluloses or modified mineral materials can also be employed with liquid carriers to form spreadable pastes, gels, ointments, soaps, and the like, for application directly to the skin of the user.

0394Examples of useful dermatological compositions which can be used to deliver the Nanobody or polypeptide to the skin are known to the art; for example, see <patcit id="pcit0106" dnum="US4608392A"><text>Jacquet et al. (U.S. Pat. No. 4,608,392</text></patcit>), <patcit id="pcit0107" dnum="US4992478A"><text>Geria (U.S. Pat. No. 4,992,478</text></patcit>), <patcit id="pcit0108" dnum="US4559157A"><text>Smith et al. (U.S. Pat. No. 4,559,157</text></patcit>) and <patcit id="pcit0109" dnum="US4820508A"><text>Wortzman (U.S. Pat. No. 4,820,508</text></patcit>).

0395Useful dosages of the Nanobody or polypeptide can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see <patcit id="pcit0110" dnum="US4938949A"><text>U.S. Pat. No. 4,938,949</text></patcit>.

0396Generally, the concentration of the Nanobody or polypeptide in a liquid composition, such as a lotion, will be from about 0.1-25 wt-%, preferably from about 0.5-10 wt-%. The concentration in a semi-solid or solid composition such as a gel or a powder will be about 0.1 - 5 wt-%, preferably about 0.5-2.5 wt-%.

0397The amount of the Nanobody or polypeptide required for use in treatment will vary with the route of administration, the nature of the condition being treated and the age and condition of the patient and will be ultimately at the discretion of the attendant physician or clinician. Also the dosage of the Nanobody or polypeptide varies depending on the target cell, tumor, tissue, graft, or organ.

0398The desired dose may conveniently be presented in a single dose or as divided doses administered at appropriate intervals, for example, as two, three, four or more sub-doses per day. The sub-dose itself may be further divided, e.g., into a number of discrete loosely spaced administrations; such as multiple inhalations from an insufflator or by application of a plurality of drops into the eye.

0399An administration regimen could include long-term, daily treatment. By "long-term" is meant at least two weeks and preferably, several weeks, months, or years of duration. Necessary modifications in this dosage range may be determined by one of ordinary skill in the art using only routine experimentation given the teachings herein. See <nplcit id="ncit0128" npl-type="b"><text>Remington's Pharmaceutical Sciences (Martin, E.W., ed. 4), Mack Publishing Co., Easton, PA</text></nplcit>. The dosage can also be adjusted by the individual physician in the event of any complication.

0400The invention provides for an agent that is a modulator of platelet-mediated aggregation.

0401The candidate agent may be a synthetic agent, or a mixture of agents, or may be a natural product (e.g. a plant extract or culture supernatant). A candidate agent according to the invention includes a small molecule that can be synthesized, a natural extract, peptides, proteins, carbohydrates, lipids etc.

0402Candidate modulator agents from large libraries of synthetic or natural agents can be screened. Numerous means are currently used for random and directed synthesis of saccharide, peptide, and nucleic acid based agents. Synthetic agent libraries are commercially available from a number of companies including Maybridge Chemical Co. (Trevillet, Cornwall, UK), Comgenex (Princeton, NJ), Brandon Associates (Merrimack, NH), and Microsource (New Milford, CT). A rare chemical library is available from Aldrich (Milwaukee, WI). Combinatorial libraries are available and can be prepared. Alternatively, libraries of natural agents in the form of bacterial, fungal, plant and animal extracts are available from e.g., Pan Laboratories (Bothell, WA) or MycoSearch (NC), or are readily producible by methods well known in the art. Additionally, natural and synthetically produced libraries and agents are readily modified through conventional chemical, physical, and biochemical means.

0403Useful agents may be found within numerous chemical classes. Useful agents may be organic agents, or small organic agents. Small organic agents have a molecular weight of more than 50 yet less than about 2,500 daltons, preferably less than about 750, more preferably less than about 350 daltons. Exemplary classes include heterocycles, peptides, saccharides, steroids, and the like. The agents may be modified to enhance efficacy, stability, pharmaceutical compatibility, and the like. Structural identification of an agent may be used to identify, generate, or screen additional agents. For example, where peptide agents are identified, they may be modified in a variety of ways to enhance their stability, such as using an unnatural amino acid, such as a D-amino acid, particularly D-alanine, by functionalizing the amino or carboxylic terminus, e.g. for the amino group, acylation or alkylation, and for the carboxyl group, esterification or amidification, or the like.

0404For primary screening, a useful concentration of a candidate agent according to the invention is from about 10 mM to about 100 µM or more (i.e. 1 mM, 10 mM, 100 mM, 1 M etc.). The primary screening concentration will be used as an upper limit, along with nine additional concentrations, wherein the additional concentrations are determined by reducing the primary screening concentration at half-log intervals (e.g. for 9 more concentrations) for secondary screens or for generating concentration curves.

0405A high throughput screening kit according to the invention comprises all the necessary means and media for performing the detection of an agent that modulates platelet-mediated aggregation by interacting with a target of the invention, such as for example vWF, or fragment thereof in the presence of a polypeptide, preferably at a concentration in the range of 1µM to 1 mM. The kit comprises the following. Recombinant cells of the invention, comprising and expressing the nucleotide sequence encoding vWF, or fragment thereof, which are grown according to the kit on a solid support, such as a microtiter plate, more preferably a 96 well microtiter plate, according to methods well known to the person skilled in the art especially as described in <patcit id="pcit0111" dnum="WO0002045A"><text>WO 00/02045</text></patcit>. Alternatively vWF, or fragment thereof is supplied in a purified form to be immobilized on, for example, a 96 well microtiter plate by the person skilled in the art. Alternatively vWF, or fragment thereof is supplied in the kit pre-immobilized on, for example, a 96 well microtiter plate. Modulator agents according to the invention, at concentrations from about 1 µM to 1 mM or more, are added to defined wells in the presence of an appropriate concentration of Nanobody or polypeptide of the invention said concentration of said polypeptide preferably in the range of 1 µM to 1 mM. Kits may contain more than one polypeptide

0406Binding assays are performed as according to the methods already disclosed herein and the results are compared to the baseline level of, for example vWF, or fragment thereof binding to a polypeptide of the invention, but in the absence of added modulator agent. Wells showing at least 2 fold, preferably 5 fold, more preferably 10 fold and most preferably a 100 fold or more increase or decrease in vWF-polypeptide binding (for example) as compared to the level of activity in the absence of modulator, are selected for further analysis.

0407The invention provides for kits useful for screening for modulators of platelet-mediated aggregation, as well as kits useful for diagnosis of diseases or disorders characterised by dysregulation platelet-mediated aggregation. Kits useful according to the invention can include an isolated vWF, or fragment thereof. Alternatively, or in addition, a kit can comprise cells transformed to express vWF, or fragment thereof. In a further embodiment, a kit according to the invention can comprise a polynucleotide encoding vWF, or fragment thereof . In a still further embodiment, a kit according to the invention may comprise the specific primers useful for amplification of vWF, or fragment thereof. Kits useful according to the invention can comprise a Nanobody or polypeptide of the invention. A kit according to the invention can comprise cells transformed to express said polypeptide. Kits may contain more than one polypeptide. In a further embodiment, a kit according to the invention can comprise a polynucleotide encoding a macromolecule, for example, vWF, or fragment thereof. In a still further embodiment, a kit according to the invention may comprise the specific primers useful for amplification of a macromolecule such as, for example, vWF, or fragment thereof. All kits according to the invention will comprise the stated items or combinations of items and packaging materials therefore. Kits will also include instructions for use.

0408The invention also provides for invasive medical devices coated with a Nanobody or polypeptide of the invention or an agent resulting from a screening method of the invention for use in devices requiring the same. Non-limiting examples of devices include surgical tubing, occlusion devices, prosthetic devices. Application for said devices include surgical procedures which require a modulation of platelet-mediated aggregation around the site of invasion.

0409One embodiment of the present is a method for treating invasive medical devices to prevent platelet-mediate aggregation around the site of invasion comprising the step of coating said device with a Nanobody or polypeptide of the invention or agent according to the invention.

0410Another embodiment of the present is a invasive medical devices that circumvents platelet-mediate aggregation around the site of invasion, wherein said device is coated with a Nanobody or polypeptide of the invention or agent according to the invention.

0411In another aspect, the invention relates to a method for the prevention and/or treatment of at least one aggregation-mediated disorder (as described herein), said method comprising administering, to a subject in need thereof, a pharmaceutically active amount of a Nanobody of the invention, of a polypeptide of the invention, and/or of a pharmaceutical composition comprising the same.

0412In the context of the present invention, the term "prevention and/or treatment" not only comprises preventing and/or treating the disease, but also generally comprises preventing the onset of the disease, slowing or reversing the progress of disease, preventing or slowing the onset of one or more symptoms associated with the disease, reducing and/or alleviating one or more symptoms associated with the disease, reducing the severity and/or the duration of the disease and/or of any symptoms associated therewith and/or preventing a further increase in the severity of the disease and/or of any symptoms associated therewith, preventing, reducing or reversing any physiological damage caused by the disease, and generally any pharmacological action that is beneficial to the patient being treated.

0413The subject to be treated may be any warm-blooded animal, but is in particular a mammal, and more in particular a human being. As will be clear to the skilled person, the subject to be treated will in particular be a person suffering from, or at risk from, the diseases and disorders mentioned herein.

0414The invention also relates to a method for the prevention and/or treatment of at least one disease or disorder that can be prevented and/or treated by administering a Nanobody or polypeptide of the invention to a patient, said method comprising administering, to a subject in need thereof, a pharmaceutically active amount of a Nanobody of the invention, of a polypeptide of the invention, and/or of a pharmaceutical composition comprising the same.

0415More in particular, the invention relates to a method for the prevention and/or treatment of at least one disease or disorder chosen from the group consisting of the diseases and disorders listed herein, said method comprising administering, to a subject in need thereof, a pharmaceutically active amount of a Nanobody of the invention, of a polypeptide of the invention, and/or of a pharmaceutical composition comprising the same.

0416In another embodiment, the invention relates to a method for immunotherapy, and in particular for passive immunotherapy, which method comprises administering, to a subject suffering from or at risk of the diseases and disorders mentioned herein, a pharmaceutically active amount of a Nanobody of the invention, of a polypeptide of the invention, and/or of a pharmaceutical composition comprising the same.

0417In the above methods, the Nanobodies and/or polypeptides of the invention and/or the compositions comprising the same can be administered in any suitable manner, depending on the specific pharmaceutical formulation or composition to be used. Thus, the Nanobodies and/or polypeptides of the invention and/or the compositions comprising the same can for example be administered orally, intraperitoneally (e.g. intravenously, subcutaneously, intramuscularly, or via any other route of administration that circumvents the gastrointestinal tract), intranasally, transdermally, topically, by means of a suppository, by inhalation, again depending on the specific pharmaceutical formulation or composition to be used. The clinician will be able to select a suitable route of administration and a suitable pharmaceutical formulation or composition to be used in such administration, depending on the disease or disorder to be prevented or treated and other factorse well known to the clinician.

0418As mentioned herein and as will be clear to the skilled person, for acute conditions and complications (i.e. as may occur with some of the aggregation-mediated disorders mentioned herein), usually administration directly into the blood stream such by infusion or injection or any other suitable means will be preferred.

0419The Nanobodies and/or polypeptides of the invention and/or the compositions comprising the same are administered according to a regime of treatment that is suitable for preventing and/or treating the disease or disorder to be prevented or treated. The clinician will generally be able to determine a suitable treatment regimen, depending on factors such as the disease or disorder to be prevented or treated, the severity of the disease to be treated and/or the severity of the symptoms thereof, the specific Nanobody or polypeptide of the invention to be used, the specific route of administration and farmaceutical formulation or composition to be used, the age, gender, weight, diet, general condition of the patient, and similar factors well known to the clinician.

0420Generally, the treatment regimen will comprise the administration of one or more Nanobodies and/or polypeptides of the invention, or of one or more compositions comprising the same, in one or more pharmaceutically effective amounts or doses. The specific amount(s) or doses to administered can be determined by the clinician, again based on the factors cited above.

0421Generally, for the prevention and/or treatment of the diseases and disorders mentioned herein and depending on the specific disease or disorder to be treated, the potency of the specific Nanobody and polypeptide of the invention to be used, the specific route of administration and the specific pharmaceutical formulation or composition used, the Nanobodies and polypeptides of the invention will generally be administered in an amount between 1 gram and 0.01 microgram per kg body weight per day, preferably between 0.1 gram and 0.1 microgram per kg body weight per day, such as about 1, 10, 100 or 1000 microgram per kg body weight per day, either continuously (e.g. by infusion), as a single daily dose or as multiple divided doses during the day. The clinician will generally be able to determine a suitable daily dose, depending on the factors mentioned herein. It will also be clear that in specific cases, the clinician may choose to deviate from these amounts, for example on the basis of the factors cited above and his expert judgment. Generally, some guidance on the amounts to be administered can be obtained from the amounts usually administered for comparable conventional antibodies or antibody fragments against the same target administered via essentially the same route, taking into account however differences in affinity/avidity, efficacy, biodistribution, half-life and similar factors well known to the skilled person.

0422Usually, in the above method, a single Nanobody or polypeptide of the invention will be used. It is however within the scope of the invention to use two or more Nanobodies and/or polypeptides of the invention in combination.

0423The Nanobodies and polypeptides of the invention may also be used in combination with one or more further pharmaceutically active compounds or principles, i.e. as a combined treatment regimen, which may or may not lead to a synergistic effect. Again, the clinician will be able to select such further compounds or principles, as well as a suitable combined treatment regimen, based on the factors cited above and his expert judgement.

0424In particular, the Nanobodies and polypeptides of the invention may be used in combination with other pharmaceutically active compounds or principles that are or can be used for the prevention and/or treatment of the diseases and disorders cited herein, as a result of which a synergistic effect may or may not be obtained. Examples of such compounds and principles, as well as routes, methods and pharmaceutical formulations or compositions for administering them will be clear to the clinician, and for example include, but are not limited to heparin, aspirin (e.g. Aspegic®), Plavix and/or Reopro.

0425When two or more substances or principles are to be used as part of a combined treatment regimen, they can be administered via the same route of administration or via different routes of administration, at essentially the same time or at different times (e.g. essentially simultaneously, consecutively, or according to an alternating regime). When the substances or principles are administered to be simultaneously via the same route of administration, they may be administered as different pharmaceutical formulations or compositions or part of a combined pharmaceutical formulation or composition, as will be clear to the skilled person.

0426Also, when two or more active substances or principles are to be used as part of a combined treatment regimen, each of the substances or principles may be administered in the same amount and according to the same regimen as used when the compound or principle is used on its own, and such combined use may or may not lead to a synergistic effect. However, when the combined use of the two or more active substances or principles leads to a synergistic effect, it may also be possible to reduce the amount of one, more or all of the substances or principles to be administered, while still achieving the desired therapeutic action. This may for example be useful for avoiding, limiting or reducing any unwanted side-effects that are associated with the use of one or more of the substances or principles when they are used in their usual amounts, while still obtaining the desired pharmaceutical or therapeutic effect.

0427The effectiveness of the treatment regimen used according to the invention may be determined and/or followed in any manner known per se for the disease or disorder involved, as will be clear to the clinician. The clinician will also be able, where appropriate and or a case-by-case basis, to change or modify a particular treatment regimen, so as to achieve the desired therapeutic effect, to avoid, limit or reduce unwanted side-effects, and/or to achieve an appropriate balance between achieving the desired therapeutic effect on the one hand and avoiding, limiting or reducing undesired side effects on the other hand.

0428The subject to be treated may be any warm-blooded animal, but is in particular a mammal, and more in particular a human being. As will be clear to the skilled person, the subject to be treated will in particular be a person suffering from, or at risk from, the diseases and disorders mentioned herein.

0429The invention also relates to the use of a Nanobody or polypeptide of the invention in the preparation of a pharmaceutical composition for the prevention and/or treatment of at least one disease or disorder (e.g. an aggregation disorder as mentioned herein) that can be prevented and/or treated by administering a Nanobody or polypeptide of the invention to a patient.

0430Generally, the treatment regimen will be followed until the desired therapeutic effect is achieved and/or for as long as the desired therapeutic effect is to be maintained. Again, this can be determined by the clinician.

0431Finally, it will also be clear to the skilled person that it may be possible to "graft" one or more of the CDR's mentioned above for the Nanobodies of the invention onto other "scaffolds", including but not limited to human scaffolds or non-immunoglobulin scaffolds. Suitable scaffolds and techniques for such CDR grafting will be clear to the skilled person and are well known in the art, see for example <patcit id="pcit0112" dnum="US7180370A"><text>US-A-7,180,370</text></patcit>, <patcit id="pcit0113" dnum="WO0127160A"><text>WO 01/27160</text></patcit>, <patcit id="pcit0114" dnum="EP0605522A"><text>EP 0 605 522</text></patcit>, <patcit id="pcit0115" dnum="EP0460167A"><text>EP 0 460 167</text></patcit>, <patcit id="pcit0116" dnum="US7054297A"><text>US-A-7,054,297</text></patcit>, <nplcit id="ncit0129" npl-type="s"><text>Nicaise et al., Protein Science (2004), 13:1882-1891</text></nplcit>; <nplcit id="ncit0130" npl-type="s"><text>Ewert et al., Methods, 2004 Oct; 34(2):184-199</text></nplcit>; <nplcit id="ncit0131" npl-type="s"><text>Kettleborough et al., Protein Eng. 1991 Oct; 4(7): 773-783</text></nplcit>; <nplcit id="ncit0132" npl-type="s"><text>O'Brien and Jones, Methods Mol. Biol. 2003: 207: 81-100</text></nplcit>; and <nplcit id="ncit0133" npl-type="s"><text>Skerra, J. Mol. Recognit. 2000: 13: 167-187</text></nplcit>, and <nplcit id="ncit0134" npl-type="s"><text>Saerens et al., J. Mol. Biol. 2005 Sep 23;352(3):597-607</text></nplcit>, and the further references cited therein; and also include for example the framework regions of other (single) domain antibodies. For example, techniques known per se for grafting mouse or rat CDR's onto human frameworks and scaffolds can be used in an analogous manner to provide chimeric proteins comprising one or more of the CDR's of the Nanobodies of the invention and one or human framework regions or sequences.

0432Thus, in another embodiment, the invention comprises a chimeric polypeptide comprising at least one CDR sequence chosen from the group consisting of CDR1 sequences, CDR2 sequences and CDR3 sequences mentioned herein for the Nanobodies of the invention. Preferably, such a chimeric polypeptide comprises at least one CDR sequence chosen from the group consisting of the CDR3 sequences mentioned herein for the Nanobodies of the invention, and optionally also at least one CDR sequence chosen from the group consisting of the CDR1 sequences and CDR2 sequences mentioned herein for the Nanobodies of the invention. For example, such a chimeric polypeptide may comprise one CDR sequence chosen from the group consisting of the CDR3 sequences mentioned herein for the Nanobodies of the invention, one CDR sequence chosen from the group consisting of the CDR1 sequences mentioned herein for the Nanobodies of the invention and one CDR sequence chosen from the group consisting of the CDR1 sequences and CDR2 sequences mentioned herein for the Nanobodies of the invention. The combinations of CDR's that are mentioned herein as being preferred for the Nanobodies of the invention will usually also be preferred for these chimeric polypeptides.

0433In said chimeric polypeptides, the CDR's may be linked to further amino acid sequences sequences and/or may be linked to each other via amino acid sequences, in which said amino acid sequences are preferably framework sequences or are amino acid sequences that act as framework sequences, or together form a scaffold for presenting the CDR's. Reference is again made to the prior art mentioned in the last paragraph. According to one preferred embodiment, the amino acid sequences are human framework sequences, for example V_H3 framework sequences. However, non-human, synthetic, semi-synthetic or non-immunoglobulin framework sequences may also be used. Preferably, the framework sequences used are such that (1) the chimeric polypeptide is capable of binding xxxx, i.e. with an affinity that is at least 1%, preferably at least 5%, more preferably at least 10%, such as at least 25% and up to 50% or 90% or more of the affinity of the corresponding Nanobody of the invention; (2) the chimeric polypeptide is suitable for pharmaceutical use; and (3) the chimeric polypeptide is preferably essentially non-immunogenic under the intended conditions for pharmaceutical use (i.e. indication, mode of administration, dosis and treatment regimen) thereof (which may be essentially analogous to the conditions described herein for the use of the Nanobodies of the invention).

0434According to one non-limiting embodiment, the chimeric polypeptide comprises at least two CDR sequences (as mentioned above) linked via at least one framework sequence, in which preferably at least one of the two CDR sequences is a CDR3 sequence, with the other CDR sequence being a CDR1 or CDR2 sequence. According to a preferred, but non-limiting embodiment, the chimeric polypeptide comprises at least two CDR sequences (as mentioned above) linked at least two framework sequences, in which preferably at least one of the three CDR sequences is a CDR3 sequence, with the other two CDR sequences being CDR1 or CDR2 sequences, and preferably being one CDR1 sequence and one CDR2 sequence. According to one specifically preferred, but non-limiting embodiment, the chimeric polypeptides have the structure FR1' - CDR1 - FR2' - CDR2 - FR3' - CDR3 - FR4', in which CDR1, CDR2 and CDR3 are as defined herein for the CDR's of the Nanobodies of the invention, and FR1', FR2', FR3' and FR4' are framework sequences. FR1', FR2', FR3' and FR4' may in particular be Framework 1, Framework 2, Framework 3 and Framework 4 sequences, respectively, of a human antibody (such as V_H3 sequences) and/or parts or fragments of such Framework sequences. It is also possible to use parts or fragments of a chimeric polypeptide with the structure FR1' - CDR1 - FR2' - CDR2 - FR3' - CDR3 - FR4. Preferably, such parts or fragments are such that they meet the criteria set out in the preceding paragraph.

0435The invention will now be further described by means of the following non-limiting examples and figures, in which the Figures show: <ul id="ul0080" list-style="none" compact="compact"><li><figref idref="f0001">Figure 1</figref>: Binding of nanobodies to vWF in ELISA</li><li><figref idref="f0001">Figure 2</figref>: Alignment of 12A5 homologue nanobody sequences</li><li><figref idref="f0001">Figure 3</figref>: Alignment of 12B6 homologue nanobody sequences</li><li><figref idref="f0002">Figure 4</figref>: Binding of 12A5 homologue nanobodies to vWF in BIACORE</li><li><figref idref="f0002">Figure 5</figref>: Binding of 12B6 homologue nanobodies to vWF in BIACORE</li><li><figref idref="f0003">Figure 6</figref>: Platelet adhesion at different concentrations of 12B6, 12A2 and 12A5 nanobodies</li><li><figref idref="f0003">Figure 7a</figref>: Binding in ELISA to vWF for 12B6 nanobody after heating at increasing temperatures</li><li><figref idref="f0004">Figure 7b</figref>: Binding in ELISA to vWF for 12A2 nanobody after heating at increasing temperatures</li><li><figref idref="f0004">Figure 7c</figref>: Binding in ELISA to vWF for 12A5 nanobody after heating at increasing temperatures</li><li><figref idref="f0005">Figure 8a</figref>: Binding of vWF from different species to 12B6 nanobody in ELISA</li><li><figref idref="f0005">Figure 8b</figref>: Binding of vWF from different species to 12A2 nanobody in ELISA</li><li><figref idref="f0006">Figure 8c</figref>: Binding of vWF from different species to 12A5 nanobody in ELISA</li><li><figref idref="f0006">Figure 9</figref>: Binding of bivalent 12B6 nanobodies to vWF in BIACORE</li><li><figref idref="f0007">Figure 10</figref>: Binding of bivalent 12A2 nanobodies to vWF in BIACORE</li><li><figref idref="f0007">Figure 11</figref>: Binding of bivalent 12A5 nanobodies to vWF in BIACORE</li><li><figref idref="f0008 f0009">Figure 12</figref>: Binding in ELISA to vWF of bivalent 12B6 nanobodies after heating at increasing temperatures</li><li><figref idref="f0010 f0011">Figure 13</figref>: Binding in ELISA to vWF of bivalent 12A2 nanobodies after heating at increasing temperatures</li><li><figref idref="f0012 f0013">Figure 14</figref>: Binding in ELISA to vWF of bivalent 12A5 nanobodies after heating at increasing temperatures</li><li><figref idref="f0014">Figure 15</figref>: Alignment of humanised 12B6 nanobody sequences</li><li><figref idref="f0014">Figure 16</figref>: Binding in ELISA to vWF of wild type and humanised 12B6 nanobody</li><li><figref idref="f0015">Figure 17</figref>: Alignment of humanised 12A2 nanobody sequences</li><li><figref idref="f0016 f0017">Figure 18</figref>: Binding in ELISA to vWF of humanised 12A2 nanobodies, after heating at increasing temperatures</li><li><figref idref="f0018">Figure 19</figref>: Binding in ELISA to vWF of humanised 12A2 nanobodies</li><li><figref idref="f0018">Figure 20</figref>: Alignment of humanised 12A5 nanobody sequences</li><li><figref idref="f0019">Figure 21</figref>: Binding in ELISA to vWF of wild type and humanised 12A5 nanobody</li><li><figref idref="f0019">Figure 22</figref>: Alignment of nanobodies selected for bivalent form</li><li><figref idref="f0020">Figure 23</figref>: Platelet adhesion at different concentrations of bivalent (humanised) nanobodies</li><li><figref idref="f0020">Figure 24</figref>: Blood flow pattern for Folts model in baboons</li><li><figref idref="f0020">Figure 25</figref>: Experimental setup for Folts model in baboons</li><li><figref idref="f0021">Figure 26</figref>: Folts study of baboon control group. The blood flow in function of time is shown, indicating the CFRs (representative of 2 independent experiments)</li><li><figref idref="f0022">Figure 27</figref>: Folts study of baboon group treated with Aspegic. The blood flow in function of time is shown, indicating the CFRs (representative of 3 independent experiments)</li><li><figref idref="f0023">Figure 28</figref>: study of baboon group treated with Heparin. The blood flow in function of time is shown, indicating the CFRs (representative of 3 independent experiments)</li><li><figref idref="f0024">Figure 29</figref>: Folts study of baboon group treated with Plavix. The blood flow in function of time is shown, indicating the CFRs (representative of 4 independent experiments)</li><li><figref idref="f0025">Figure 30</figref>: Folts study of baboon group treated with Reopro. The blood flow in function of time is shown, indicating the CFRs (representative of 3 independent experiments)</li><li><figref idref="f0026">Figure 31</figref>: Folts study of baboon group treated with ALX-0081 (SEQ ID NO:98). The blood flow in function of time is shown, indicating the CFRs (representative of 8 independent experiments)</li><li><figref idref="f0027">Figure 32</figref>: Flow read out from baboon ID 6 treated with a combination of Aspegic, Heparin, Plavix and ALX-0081</li><li><figref idref="f0028">Figure 33</figref>: Averages of relative blood loss in function of different doses of Plavix, Reopro and ALX-0081</li><li><figref idref="f0029">Figure 34</figref>: Average length of CFRs and average relative amount of blood loss for animals treated with Plavix in function of increasing drug dose.</li><li><figref idref="f0030">Figure 35</figref>: Average length of CFRs and average relative amount of blood loss for animals treated with Reopro in function of increasing drug dose</li><li><figref idref="f0031">Figure 36</figref>: Average length of CFRs and average relative amount of blood loss for animals treated with ALX-0081 in function of increasing drug dose</li><li><figref idref="f0032 f0033 f0034 f0035 f0036">Figure 37</figref>: ristocetin-induced aggregation (%, ■) and length of CFRs (s, ◆) for each baboon treated with ALX-0081 in function of all doses</li><li><figref idref="f0037">Figure 38</figref>: Concentration of ALX-0081 in plasma versus the length of CFRs for all baboons treated with ALX-0081</li><li><figref idref="f0038">Figure 39</figref>: Concentration of ALX-0081 in plasma versus relative amount of blood loss from the gauzes</li><li><figref idref="f0039">Figure 40</figref>: Folts study of baboon 1 treated with ALX-0081 and vWF. The blood flow in function of time is shown, indicating the CFRs</li><li><figref idref="f0040">Figure 41</figref>: strings (arrows) of adhered platelets on ULvWF secreted from stimulated endothelial cells</li><li><figref idref="f0040">Figure 42</figref>: Absence of strings when platelets are perfused over ULvWF in the presence of ALX-0081</li><li><figref idref="f0040">Figure 43</figref>: Control perfusion experiment: ULvWF strings before (panel A, indicated with red arrows) and during (panel B) perfusion with normal plasma. In panel B,, ULvWF strings being cleaved by ADAMTS-13 are indicated with a blue and red arrow for a piece of an ULvWF string moving away or for largely cleaved ULvWF strings respectively</li><li><figref idref="f0041">Figure 44</figref>: Perfusion experiment in presence of ALX-0081. Microscopic image of a field before (panel A) and of the same field after (panel B) perfusion with normal plasma. An UlvWF string is indicated in panel A with a red arrow which is absent in panel B due to cleavage of the ULvWF by ADAMTS-13.</li><li>Figure 45: cleavage of A1-A2-A3 by ADAMTS-13 present in normal pool plasma (NPP) in the absence and presence of ALX-0081</li></ul><b>and in which the Tables, which form an integral part of the present description, are as follows:</b><ul id="ul0081" list-style="none" compact="compact"><li>Table 8: Sequence listing of anti-vWF nanobodies</li><li>Table 9: Expression yields of anti-vWF nanobodies</li><li>Table 10: Platelet adhesion in perfusion chamber of anti-vWF nanobodies</li><li>Table 11: Sequence listing of 12B6 and 12A5 homologue nanobodies</li><li>Table 12: Estimated K-on, K-off and KD values for 12A5 homologue nanobodies</li><li>Table 13: Estimated K-on, K-off and KD values for 12B6 homologue nanobodies</li><li>Table 14: Real KD value of 12B6, 12A2 and 12A5 nanobodies</li><li>Table 15: Platelet adhesion in perfusion chamber of 12B6, 12A2 and 12A5 nanobodies</li><li>Table 16: Concentration of 12B6, 12A2 and 12A5 nanobodies after heating at increasing temperatures</li><li>Table 17: Sequence listing of bivalent nanobodies</li><li>Table 18: Sequence listing of linker sequences</li><li>Table 19: Expression yields of bivalent 12B6, 12A2 and 12A5 nanobodies</li><li>Table 20: Concentration of 12B6 bivalent nanobodies after heating at increasing temperatures</li><li>Table 21: Concentration of 12A2 bivalent nanobodies after heating at increasing temperatures</li><li>Table 22: Concentration of 12A5 bivalent nanobodies after heating at increasing temperatures</li><li>Table 23: Platelet adhesion in perfusion chamber of 12A2 bivalent nanobodies</li><li>Table 24: Sequence listing of humanised 12B6 nanobodies</li><li>Table 25: Expression yields of wild type and humanised 12B6 nanobodies</li><li>Table 26: Concentration of wild type and humanised 12B6 nanobodies after heating at increasing temperatures</li><li>Table 27: KD values for wild type and humanised 12B6 nanobodies</li><li>Table 28: Sequence listing of humanised 12A2 nanobodies</li><li>Table 29: Expression yields of wild type and humanised 12A2 nanobodies</li><li>Table 30: Concentration of wild type and humanised 12A2 nanobodies after heating at increasing temperatures</li><li>Table 31: Platelet adhesion of wild type and humanised 12A2 nanobodies in perfusion chamber at 0.7 and 1.5 ug/ml</li><li>Table 32: Platelet adhesion of wild type and humanised 12A2 nanobodies in perfusion chamber at 0.5, 1 and 2 ug/ml</li><li>Table 33: KD values for wild type and humanised 12A2 nanobodies</li><li>Table 34: Sequence listing of humanised 12A5 nanobodies</li><li>Table 35: Expression yields of wild type and humanised 12A5 nanobodies</li><li>Table 36: Concentration of wild type and humanised 12A5 nanobodies after heating at increasing temperatures</li><li>Table 37: KD values for wild type and humanised 12A5 nanobodies</li><li>Table 38: Sequence listing of humanised bivalent nanobodies</li><li>Table 39: Expression yields of humanised bivalent nanobodies</li><li>Table 40: Concentration of humanised bivalent nanobody after heating at increasing temperatures</li><li>Table 41: Platelet adhesion of wild type and humanised bivalent nanobodies</li><li>Table 42: baboons used with the different test compounds in the Folts study</li><li>Table 43: Length of CFRs (s) for control animals (ND= not done)</li><li>Table 44: Length of CFRs (s) for animals treated with Aspegic™ (ND= not done)</li><li>Table 45: Length of CFRs (s) for animals treated with Heparin™ (ND= not done)</li><li>Table 46: Length of CFRs (s) for animals treated with Plavix™ (ND= not done)</li><li>Table 47: Length of CFRs (s) for animals treated with Reopro™ (ND= not done)</li><li>Table 48: Length of CFRs (s) for animals treated with ALX-0081 (ND= not done)</li><li>Table 49: baboons used with the different test compounds in the Folts study</li><li>Table 50: Inhibition of CFRs in the Folts model for the different drugs tested. The number of experiments in which an inhibition of CFRs was observed in the mentioned different conditions is shown as a function of the total number of independent repeats of that condition.</li><li>Table 51: Length of CFRs (seconds) for each baboon and each dose of Aspegic, Heparin, Plavix and ALX-0081. The effective dose is indicated in yellow</li><li>Table 52: Blood loss relative to the second control gauze for animals treated with Plavix™ in function of final dose (STD= standard deviation)</li><li>Table 53: Blood loss relative to the second control gauze for animals treated with Reopro™ in function of final dose (STD= standard deviation)</li><li>Table 54: Blood loss relative to the second control gauze for animals treated with ALX-0081in function of final dose (STD= standard deviation)</li><li>Table 55: The average of the total amount of blood loss (= sum of blood loss from the first five doses of test compound) as relative to the second control gauze</li><li>Table 56: Blood loss in gauzes relative to the second control gauze for each baboon treated with Aspegic, Heparin, Plavix and ALX-0081 in function of drug dose. The effective drug dose in which a complete inhibition of CFRs was observed, is indicated in yellow</li><li>Table 57: % ristocetin-induced platelet aggregation for each baboon treated with Aspegic, Heparin, Plavix and ALX-0081 in function of drug dose</li><li>Table 58: concentration of ALX-0081 [µg/ml] in blood samples obtained at 10 minutes after administration</li><li>Table 59: Length of CFRs [seconds] for baboons treated with ALX-0081 and with vWF Table 60: Volumes [µl] to prepare the different mixtures for study of cleavage of A1A2A3 by ADAMTS13.</li></ul>

EXAMPLES

<u>A. Selection and screening of nanobodies specific for vWF and inhibiting platelet adhesion</u>

Example 1: Antigen specific monovalent nanobodies

0436The nanobodies represented in Table 8 SEQ ID Nos: 60 to 66 are obtained from llamas immunized with human vWF or with recombinant A1 domain of vWF. The nanobodies bind to the A1 domain of vWF and inhibit the interaction between vWF and gpIb on the platelets.

Example 2: Expression and purification of nanobodies

0437Plasmid was prepared (QIAGEN, according to the manufacturers instructions) and was transformed into WK6 or TC1 electro-competent cells. A single colony was used to start an overnight culture in LB containing 2% glucose and 100 µg/ml ampicillin. This overnight culture was diluted 100-fold in 2x300 ml TB medium containing 100 µg/ml ampicillin, and incubated at 37°C until OD600nm= 0.5. 1 mM IPTG was added and the culture was incubated for 3 more hours at 37°C or overnight at 28°C.

0438Cultures were centrifuged for 20 minutes at 10000 rpm at 4°C. The pellet was frozen overnight or for 1 hour at -20°C. Next, the pellet was thawed at room temperature for 40 minutes, resuspended in 20 ml peri buffer (50 mM NaH₂PO₄ and 300 mM NaCl) and shaken at room temperature for 1 hour. Periplasmic fraction was isolated by centrifugation for 20 minutes at 4°C at 20000 rpm. The nanobodies were purified on a Nickel column (TALON, Clonetech) as described by the manufacturer and expression yields were calculated as represented in Table 9.

Example 3: Binding of nanobodies to vWF in ELISA

0439The nanobodies of Example 1 were tested for binding to vWF in ELISA. Therefore, a microtiterplate (Nunc, Maxisorb) was coated with vWF (Red Cross) at a 200-fold dilution and pre-warmed for 15 minutes at 37°C. The plate was coated overnight at 4°C. The plate was then washed with PBS-Tween and blocked for two hours at room temperature with PBS-1% casein. After washing, the samples were applied starting at a concentration of 10 µg/ml and 3-fold dilutions were made in PBS. After a two hours incubation period, the plates were washed and mouse monoclonal anti-myc antibody at a 1000-fold dilution was applied for 1 hour at room temperature. The plates were washed and polyclonal anti-mouse-HRP (DAKO) was applied at a 1000-fold dilution for one hour at room temperature. The plates were washed and ABTS/H₂O₂ substrate was applied. The OD 405 nm was measured. Results are shown in <figref idref="f0001">Figure 1</figref>.

Example 4: Inhibition of platelet adhesion by nanobodies in a flow chamber

0440The protein samples were analysed in a perfusion chamber. Thermanox coverslips (Nunc) were soaked overnight in 80 % ethanol, rinsed thoroughly with distilled water and air-dried. Human placental collagen type III (Sigma) was solubilized in 0.05 mol/l acetic acid and sprayed on the coverslips at a final density of 30µg/cm² with a retouching airbrush. After spraying the coverslips were blocked with 1% human albumin solution in PBS for at least 1 hour at RT. Perfusions were performed with a single-pass perfusion chamber under non-pulsatile flow conditions using a modified small perfusion chamber with a slit height of 0.1 mm and a slit width of 2 mm. Blood was obtained by venipuncture from healthy volunteers and anti-coagulated with Penta/PPACK. Triplicate coverslips were inserted into the chamber. Five milliliters of blood was pre-warmed at 37°C for 5 minutes with or without addition of 2 microgram/ml nanobody and then circulated through the chamber for 5 minutes at a wall shear rate of 1600 s^-1 using an infusion pump. After a perfusion run, the coverslip was taken from the chamber, rinsed in Hepes buffered saline (10 mM Hepes, 150 mM NaCL, ph 7.4), fixed in 0.5% glutaraldehyde in PBS, dehydrated in methanol and stained with May-Grünwald and Giemsa (Riedel de Haën). Platelet deposition was evaluated as platelet surface coverage using light microscopy and computer-assisted analysis. Results are shown in Table 10. Nanobodies 12B6 and 12A5 clearly inhibit platelet adhesion to collagen type III in the perfusion chamber at high shear rate.

Example 5: Analysis in BIACORE for binding to vWF for homologues nanobodies

0441Nanobodies 12B6 and 12A5 inhibit platelet adhesion in the perfusion chamber. Homologue sequences were obtained from the llama comprising the amino acid differences as shown in Table 11 SEQ ID Nos 67 to 73. <figref idref="f0001">Figure 2 and 3</figref> represent the alignment of the 12A5 and 12B6 homologue nanobody sequences.

0442vWF was covalently bound to the sensor chip surface via amine coupling. The CM5 surface of the chip was activated by the injection of EDC/NHS (1:1 mix of 0,4 M 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and 0,1 M N-hydroxysuccinimide in water) for 7 minutes. Upon activation vWF was injected until an increase of 6000 response units was detected. The excess of reactive groups was deactivated with 1 M Ethanolamine-HCl (pH 8,5) for 7 minutes. The flowrate was kept constant during the immobilization procedure at 5 ul/min. The eluent buffer was 0,01 M HEPES (pH 7,4) with 0,15 M NaCl, 3 mM EDTA and 0,005 % Surfactant P20.

0443The nanobodies 12B6 and 12A5 and their homologue proteins were analysed in BIACORE on vWF at a concentration of the nanobody of 5 µg/ml as shown in <figref idref="f0002">Figure 4 and 5</figref>. Estimated kon, K-off and KD values are represented in Table 12 and 13. Nanobodies 12A5 and 12B5 have the best K-on and K-off rates. Nanobodies 12A2 and 12B6 have the best K-on rate, the K-off rates are very comparable for all nanobodies tested.

0444Table 14 shows the real KD value for vWF on BIACORE using a range of concentrations of the nanobodies. From the set of curves that were generated for each nanobody, only those curves where equilibrium was reached, were used to derive the KD value via steady state affinity.

0445For the treatment of acute events, the fast inhibition of vWF is very important, and thus a fast K-on rate is preferred. The K-on rate determines how fast a nanobody binds its target (vWF) when injected into human or animals.

Example 6: Compare inhibiting nanobodies for potency in the perfusion chamber

0446To compare the potency for inhibition of platelet adhesion, the nanobodies 12A2, 12B6 and 12A5 were tested in the perfusion chamber at 0.2, 0.4 and 0.6 µg/ml. The experiment was performed using the same donor for all nanobodies. Results are shown in Table 15 and <figref idref="f0003">Figure 6</figref>. The nanobodies show a very comparable inhibiting capacity in the perfusion chamber, with full inhibition of platelet adhesion at a concentration of 0.6 µg/ml nanobody.

Example 7: Stability of nanobodies at elevated temperatures

0447A stock solution of nanobodies at a concentration of 200 µg/ml in PBS was prepared and divided into several tubes. Each tube containing nanobody was incubated at different temperatures for 1 hour, then cooled at room temperature for 2 hours and put at 4°C overnight. The next day, the samples were centrifuged for 30 minutes at 13000 rpm, and the supernatant was tested for OD280 nm. The concentration of supernatants were measured spectophotometrically and expressed as a percentage of the concentration at room temperature. The results are summarized in Table 16.

0448The supernatants were also tested in ELISA for binding to vWF as described above in Example 3. As shown in <figref idref="f0003">Figure 7a</figref> (12B6), 7b (12A2) and 7c (12A5), the nanobodies are very stable at elevated temperatures.

Example 8: Cross-reactivity of the nanobodies with vWF from other species

0449A microtiterplate was coated with mouse anti-myc at 1/1000 overnight at 4°C. The plate was washed with PBS-Tween and blocked for two hours at room temperature with PBS-1% casein. After washing, the nanobodies were applied at a concentration of 10 µg/ml in PBS. After a one hour incubation period, the plates were washed and plasma (dog, pig, human, baboon and cynomologues monkey) was applied starting at a five-fold dilution and making further two-fold dilutions in PBS. The plates were incubated for 1 hour at room temperature. The plates were washed and polyclonal anti-vWF-HRP (DAKO) was applied at a 2000-fold dilution for one hour at room temperature. The plates were washed and ABTS/H₂O₂ substrate was applied. The OD 405 nm was measured.

0450As shown in <figref idref="f0005">Figure 8a</figref> (12B6), 8b (12A2) and 8c (12A5), nanobodies 12A5, 12A2 and 12B6 are cross-reactive with human, baboon and cynomologues monkey vWF. The nanobodies 12A2 and 12B6 are also cross-reactive with pig vWF. These nanobodies can therefore be tested for efficacy and safety in pigs. None of the nanobodies is cross-reactive with dog vWF.

<u>B. Construction of bivalent nanobodies specific for vWF and inhibiting platelet adhesion</u> Example 9: Amino acid sequences of the bivalent nanobodies

0451Table 17 SEQ ID Nos 74 to 82 represents bivalent nanobodies constructed for 12B6, 12A2 and 12A5. The nanobodies were linked with the linkers represented in Table 18 SEQ ID Nos 83 to 85.

Example 10: Expression and purification of the bivalent nanobodies

0452Expressions were performed as described above in Example 2. Expression yields are summarized in Table 19.

Example 11: Analysis of the bivalent nanobodies in BIACORE

0453The bivalent nanobodies of Example 9 were analyzed in BIACORE at 1,3 nM as described above in Example 5 to compare the affinities for vWF versus the monovalent nanobody. The bivalent nanobodies 12B6 (<figref idref="f0006">Figure 9</figref>), 12A2 (<figref idref="f0007">Figure 10</figref>) and 12A5 (<figref idref="f0007">Figure 11</figref>) have an improved affinity for vWF when compared to the monovalent nanobody.

Example 12: Stability of the bivalent nanobodies at elevated temperatures

0454Stability of the bivalent nanobodies was measured as described above in Example 7. The concentration (µg/ml) of the supernatants was measured and expressed as a percentage of the concentration at room temperature. The results are summarized in Table 20 (bivalent 12B6), Table 21 (bivalent 12A2) and Table 22 (bivalent 12A5).

0455The supernatants were tested in ELISA for binding to vWF as described above in Example 3. The supematants were applied starting at a 1/100 dilution and 1/5 dilutions were made in PBS. Results are shown in <figref idref="f0008 f0009">Figure 12</figref> (12B6), <figref idref="f0010 f0011">Figure 13</figref> (12A2) and <figref idref="f0012 f0013">Figure 14</figref> (12A5).

Example 13: Analysis of monovalent and bivalent 12A2 in the flow chamber

0456Nanobody 12A2 (monovalent and bivalent forms) was tested in the perfusion chamber as described above in Example 4. The experiment was performed using the same donor for all nanobodies. Results are summarized in Table 23. The bivalent nanobodies inhibit platelet adhesion more efficiently then the monovalent form.

<u>C. Humanisation of nanobodies specific for vWF and inhibiting platelet adhesion</u>

Example 14: Humanisation of 12B6 nanobody

0457Table 24 SEQ ID Nos: 86 to 89 represents four humanised 12B6 nanobodies. Table II lists the amino acid changes that were performed to achieve these sequences. <figref idref="f0014">Figure 15</figref> represents the alignment of the humanised sequences for 12B6. <tables id="tabl0030" num="0030"><table frame="all"><title>Table II: non-limiting humanizing substitutions</title><tgroup cols="11"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="12mm" /><colspec colnum="3" colname="col3" colwidth="14mm" /><colspec colnum="4" colname="col4" colwidth="14mm" /><colspec colnum="5" colname="col5" colwidth="14mm" /><colspec colnum="6" colname="col6" colwidth="14mm" /><colspec colnum="7" colname="col7" colwidth="14mm" /><colspec colnum="8" colname="col8" colwidth="14mm" /><colspec colnum="9" colname="col9" colwidth="16mm" /><colspec colnum="10" colname="col10" colwidth="14mm" /><colspec colnum="11" colname="col11" colwidth="14mm" /><thead><row><entry valign="top" /><entry valign="top"><b>Q1E</b></entry><entry valign="top"><b>A14P</b></entry><entry valign="top"><b>A17S</b></entry><entry valign="top"><b>E44G</b></entry><entry valign="top"><b>D46E</b></entry><entry valign="top"><b>R76N</b></entry><entry valign="top"><b>M77S</b></entry><entry valign="top"><b>A82bS</b></entry><entry valign="top"><b>K83R</b></entry><entry valign="top"><b>P84A</b></entry></row></thead><tbody><row><entry><b>12B6H1</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry /><entry /><entry>X</entry><entry>X</entry><entry>X</entry></row><row><entry><b>12B6H2</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry /><entry>X</entry><entry>X</entry><entry>X</entry></row><row><entry><b>12B6H3</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry>X</entry><entry /><entry>X</entry><entry>X</entry><entry>X</entry></row><row><entry><b>12B6H4</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry /><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry></row></tbody></tgroup></table></tables>

0458Expressions were performed as described in Example 2. Expression yields are summarized in Table 25.

0459The stability of the humanised nanobodies was measured as described in Example 7. Table 26 summarizes the OD280 nm concentrations (µg/ml) of the supernatants expressed as a percentage of the concentration at room temperature.

0460<figref idref="f0014">Figure 16</figref> shows the binding of humanised 12B6 nanobodies to vWF in ELISA performed as described in Example 3.

0461The affinity of humanised 12B6 nanobodies for vWF was determined in BIACORE. KD values are summarized in Table 27.

Example 15: Humanisation of 12A2 nanobody

0462Table 28 SEQ ID Nos: 90 to 94 represents five humanised 12A2 nanobodies. Tables III and IV list the following amino acid changes that were performed to achieve these sequences. <figref idref="f0015">Figure 17</figref> represents the alignment of the humanised sequences for 12A2. <tables id="tabl0031" num="0031"><table frame="all"><title>Table III: non-limiting humanizing substitutions:</title><tgroup cols="9"><colspec colnum="1" colname="col1" colwidth="19mm" /><colspec colnum="2" colname="col2" colwidth="12mm" /><colspec colnum="3" colname="col3" colwidth="12mm" /><colspec colnum="4" colname="col4" colwidth="12mm" /><colspec colnum="5" colname="col5" colwidth="14mm" /><colspec colnum="6" colname="col6" colwidth="14mm" /><colspec colnum="7" colname="col7" colwidth="14mm" /><colspec colnum="8" colname="col8" colwidth="14mm" /><colspec colnum="9" colname="col9" colwidth="14mm" /><thead><row><entry valign="top" /><entry valign="top"><b>Q1E</b></entry><entry valign="top"><b>K3Q</b></entry><entry valign="top"><b>E5V</b></entry><entry valign="top"><b>A14P</b></entry><entry valign="top"><b>A17S</b></entry><entry valign="top"><b>R27F</b></entry><entry valign="top"><b>E44G</b></entry><entry valign="top"><b>D46E</b></entry></row></thead><tbody><row><entry><b>12A2H1</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry>X</entry><entry>X</entry></row><row><entry><b>12A2H3</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry>X</entry><entry>X</entry></row><row><entry><b>12A2H4</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry>X</entry><entry>X</entry></row><row><entry><b>12A2H11</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry></row><row><entry><b>12A2H13</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry></row></tbody></tgroup></table></tables><tables id="tabl0032" num="0032"><table frame="all"><title>Table IV:</title><tgroup cols="7"><colspec colnum="1" colname="col1" colwidth="19mm" /><colspec colnum="2" colname="col2" colwidth="14mm" /><colspec colnum="3" colname="col3" colwidth="14mm" /><colspec colnum="4" colname="col4" colwidth="16mm" /><colspec colnum="5" colname="col5" colwidth="14mm" /><colspec colnum="6" colname="col6" colwidth="14mm" /><colspec colnum="7" colname="col7" colwidth="15mm" /><thead><row><entry valign="top" /><entry valign="top"><b>R76N</b></entry><entry valign="top"><b>M77S</b></entry><entry valign="top"><b>N82bS</b></entry><entry valign="top"><b>K83R</b></entry><entry valign="top"><b>P84A</b></entry><entry valign="top"><b>Q108L</b></entry></row></thead><tbody><row><entry><b>12A2H1</b></entry><entry /><entry /><entry>X</entry><entry>X</entry><entry>X</entry><entry /></row><row><entry><b>12A2H3</b></entry><entry>X</entry><entry /><entry>X</entry><entry>X</entry><entry>X</entry><entry /></row><row><entry><b>12A2H4</b></entry><entry /><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /></row><row><entry><b>12A2H11</b></entry><entry /><entry /><entry>X</entry><entry>X</entry><entry>X</entry><entry /></row><row><entry><b>12A2H13</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry></row></tbody></tgroup></table></tables>

0463Expressions were performed as described in Example 2. Expression yields are summarized in Table 29.

0464Stability of the humanised nanobodies was measured as described in Example 7. Table 30 summarizes the OD280 nm concentrations (µg/ml) of the supernatants expressed as a percentage of the concentration at room temperature. All humanised 12A2 nanobodies are very stable upon heating at increasing temperatures.

0465The ELISA of <figref idref="f0016 f0017">Figure 18</figref> and <figref idref="f0018">19</figref> was performed as described in Example 3. 12A2H1 and 12A2H4 bind very well to vWF in ELISA.

0466The nanobodies were tested in the flow chamber at a concentration of 0.7 µg/ml and 1.5 µg/ml. The same donor was used for all the experiments. The experiment was performed as described in Example 4. Results are summarized in Table 31 and 32.

0467The affinity of humanised 12A2 nanobodies for vWF was determined in BIACORE. KD values are summarized in Table 33.

Example 16: Humanisation of 12A5 nanobody

0468Table 34 SEQ ID Nos: 95 to 97 represents three humanised 12A5 nanobodies. Table V lists the amino acid changes that were performed to achieve these sequences. <figref idref="f0018">Figure 20</figref> represents the alignment of the humanised sequences for 12A5. <tables id="tabl0033" num="0033"><table frame="all"><title>Table V: non-limiting humanizing substitutions:</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="12mm" /><colspec colnum="3" colname="col3" colwidth="14mm" /><colspec colnum="4" colname="col4" colwidth="14mm" /><colspec colnum="5" colname="col5" colwidth="14mm" /><colspec colnum="6" colname="col6" colwidth="14mm" /><colspec colnum="7" colname="col7" colwidth="14mm" /><colspec colnum="8" colname="col8" colwidth="14mm" /><thead><row><entry valign="top" /><entry valign="top"><b>A1E</b></entry><entry valign="top"><b>L23A</b></entry><entry valign="top"><b>Q44G</b></entry><entry valign="top"><b>G73N</b></entry><entry valign="top"><b>P74A</b></entry><entry valign="top"><b>K83R</b></entry><entry valign="top"><b>P84A</b></entry></row></thead><tbody><row><entry><b>12A5H1</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry /><entry>X</entry><entry>X</entry></row><row><entry><b>12A5H2</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry /><entry>X</entry><entry>X</entry><entry>X</entry></row><row><entry><b>12A5H3</b></entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry><entry>X</entry></row></tbody></tgroup></table></tables>

0469Expressions were performed as described above in Example 2. Expression yields after TALON purification are summarized in Table 35 for each humanised 12A5 nanobody.

0470Stability of the humanised 12A5 nanobodies was measured as described above in Example 7. The OD280 of the supernatants was measured and expressed as percentage of the OD280 at room temperature. The results are summarized in Table 36. All humanised 12A5 nanobodies are comparably stable upon heating at increasing temperatures to the wild type.

0471ELISA was performed as described in Example 3. <figref idref="f0019">Figure 21</figref> illustrates the binding activity for vWF in ELISA.

0472The affinity of humanised 12A5 nanobodies for vWF was determined in BIACORE. KD values are summarized in Table 37.

Example 17: Bivalent humanised nanobodies

0473Three humanised nanobodies 12A2H1, 12A2H4 and 12B6H2 were selected for bivalent form with the 3a linker. The sequences of these 3 nanobodies differ only by a few amino acids as shown in <figref idref="f0019">Figure 22</figref>. Table 38 SEQ ID Nos 98 to 100 lists the sequences of the bivalent nanobodies. Table 38 SEQ ID Nos 101 - to 106 lists the sequences of humanised bivalent nanobodies linked with the GS9 and GS30 linker, respectively.

0474Expressions were performed as described in Example 2. The nanobodies containing a (His)₆-tag were purified on a Nickel column (TALON, Clonetech) as described by the manufacturer. The tag-sequence is EQKLISEEDLNGAA_HHHHHH. Nanobodies without tags were purified on protein A. Expression yields were calculated and are summarized in Table 39.

0475Stability of the humanised bivalent nanobodies was measured as described in Example 7. OD280 of the supernatants was measured and expressed as percentage of the OD280 at room temperature. The results are summarized in Table 40.

0476The nanobodies (humanised but also wild type) were tested in the flow chamber at a concentration of 0.15 µg/ml, 0.3 µg/ml and 0.6 µg/ml. The same donor was used for all the experiments. The experiment was performed as described in Example 4. <figref idref="f0020">Figure 23</figref> shows the platelet adhesion at different concentrations of bivalent nanobodies. Table 41 lists platelet adhesion of wild type and humanised bivalent nanobodies.

<u>D. Effect of (bivalent) nanobody on arterial thrombosis in a baboon FOLTS model</u>

Example 18: Baboon FOLTS model with ALX-0081

0477In this study the efficacy and safety of ALX-0081 was evaluated in a Folts thrombosis model in baboons.

0478Also, the efficacy and safety of ALX-0081 in a Folts thrombosis model in baboons was compared to other drugs currently used in the clinic, such as Reopro, Plavix, Aspegic, Heparin and Epinephrin. All these were diluted in 0.9% sodium chloride and administered as intravenous bolus injections. This study was as well designed to determine the effective dose for each of these compounds.

0479Finally, the efficacy in a Folts thrombosis model in baboons of a combination of drugs that is currently used in the clinic in a percutaneous coronary intervention (PCI) setting was tested: Aspegic, Heparin, and Plavix. We furthermore evaluated if ALX-0081 can improve the efficacy of this combination when added on top.

0480We looked at safety parameters such as induction of bleeding, vWF and factor VIII levels, and platelet count, PT, and aPTT.

Study Protocol

0481The study protocol that was applied is the original Folts model and some modifications described below (<nplcit id="ncit0135" npl-type="s"><text>Folts JD, et al, Circulation. 1976;54:365-370</text></nplcit>).

0482Healthy male or female baboons (<i>Papio ursinus</i>) were used. The animals were 8-17 kg of weight and were disease-free for at least 2 weeks prior to use. The baboons were fed with dry standard food only. The baboons were used at different time points. The weight of the baboons are summarized in table 42 (efficacy study ALX-0081 and comparison with individual drugs) and table 50 (efficacy of a combination of drugs and ALX-0081 on top of this combination).

0483Animals were anaesthetized and body temperature is maintained at 37°C with a heating table. A segment of a femoral artery was dissected free from surrounding tissue. A shunt was placed between the femoral vein and femoral artery to obtain high shear rates. The mean and phasic blood flow was recorded continuously throughout the experiment. Baseline flow was recorded for 20 minutes. The proximal dissection site of the femoral artery was then injured by applying two overlapping occlusions of the artery for 1 second using a forceps. A clamp was placed over the injured site to create an external stenosis.

0484A gradual decline in blood flow due to platelet adhesion and aggregation was observed. When flow was reduced to zero, blood flow was restored by opening the clamp to dislodge the platelet-rich thrombus. This repetitive pattern of decreasing blood flow following mechanical restoration is referred to as cyclic flow reductions (CFRs). Additional endothelial injury was repeated if needed to finally obtain stable CFRs in these baboons. The number of times the thrombus needed to be dislodged determines the number of CFRs. <figref idref="f0020">Figure 24</figref> illustrates blood flow pattern during the Folts model in baboons.

0485After a 30-minute control period of reproducible CFRs, the vehicle was administered as an internal control and CFRs were followed up for 30 more minutes. After this period, test agents (saline (n=2), Reopro (n=3), Aspegic (n=3), Plavix (n=4), Heparin (n=3) or ALX-0081 Nanobody™ (n=9)) were provided via an intravenous bolus injection (followed by a continuous infusion for ALX-0081) and monitoring was continued up to 30 minutes after drug administration. This procedure was repeated for several times with escalating doses of the test substance. The anti-thrombotic effect was quantified by comparing the length of CFRs before and after drug administration. When full inhibition of CFRs was observed, a new injury was applied in order to confirm that the inhibition was an effect of the treatment but not of a natural healing phenomenon. At the end of the experiments, Epinephrin (2.2 µg/kg/mm) was injected in order to distinguish between a weak and a strong inhibition of the CFRs. Indeed, it has been demonstrated before that CFRs reappear in the presence of Epinephrin when aspirin (a weak anti-platelet drug) is used in the same model. The setup of the experiment is illustrated <figref idref="f0020">Figure 25</figref>.

0486The length of the CFRs, after each dose of test compound are summarized in tables 43-48. Doses at which full inhibition of CFRs is obtained are shaded.

0487A representative read out of the blood flow during the Folts model experiments is shown in <figref idref="f0021 f0026">figures 26-31</figref>.

0488The results demonstrate that CFRs can be obtained in the control animals for at least 3 hours, without the need for a new injury in between. The mean length of the CFRs is 2-5 minutes and there is no effect on the length of the CFRs by injection of saline (<figref idref="f0021">figure 26</figref>, table 43).

<u>Aspegic</u>

0489Three animals were injected with Aspegic (injectable Aspirin) and looked for inhibition of CFRs. In the clinic, a bolus injection of 250 mg (± 3-5 mg/kg) is administered to the patient, just before the start of a percutaneous coronary intervention (PCI) procedure. In two animals (baboon 3 and 5) no inhibition of CFRs could be obtained at doses as high as 80 and 40 mg/kg Aspegic respectively (<figref idref="f0022">figure 27</figref>, table 44). In baboon 4, it was very difficult to establish a stable repetitive pattern of CFRs in the control phase. After several new injuries were made (this is at the time we injected saline), stable CFRs were obtained. Full inhibition of CFRs was obtained at the dose of 5 mg/kg Aspegic, but at higher doses and upon new injury, the CFRs returned, although the mean length of the CFRs was 3-4 times longer than before administration of Aspegic. After infusion of Epinephrin, the CFRs returned immediately and completely (table 44).

<u>Heparin</u>

0490Three animals were injected with unfractionated Heparin and looked for inhibition of CFRs. In the clinic, a bolus injection of 60-70 IU/kg is administered to the patient, and the aPTT (activated partial thromboplastin time) is monitored every 30 minutes. Extra Heparin is administered if the aPTT is &lt;250 seconds. In baboons 7 and 8, no inhibition of the CFRs could be obtained even not at doses as high as 240 IU/kg (<figref idref="f0023">figure 28</figref>, table 45). In baboon 6, full inhibition of the CFRs was obtained at the first dose of 15 IU/kg and at higher doses, but when we made a new injury the CFRs returned each time. At the highest dose of 240 IU/kg, CFRs were inhibited even after a new injury, but the flow was decreasing and upon infusion of Epinephrine, the CFRs returned immediately.

<u>Plavix</u>

0491Four baboons were treated with Plavix and used for the Folts study. We used Plavix as injectable drug by re-suspending tablets in methanol. Therefore, we were able to perform a dose escalation experiment as for the other drugs. In patients, 300-600 mg Plavix is administered orally, inhibition of platelet aggregation can be seen 2 hours after single oral doses of Plavix. Already at the 2.5 mg/kg final dose in the baboons, an effect on the length of the CFRs could be demonstrated, but this inhibitory effect started only 10 minutes after injection (<figref idref="f0024">figure 29</figref>, table 46). In baboon 12, full inhibition of the CFRs was obtained at this dose of 2,5 mg/kg. In the other three baboons full inhibition of CFRs was obtained at the 5 mg/kg final dose. CFRs remained inhibited when a new injury was made, but returned after infusion of Epinephrin. When Epinephrin infusion was stopped, the CFRs remained for another 5 minutes, but then again full inhibition was obtained (<figref idref="f0024">figure 29</figref>).

<u>Reopro</u>

0492Reopro was tested for efficacy in the Folts model in three baboons. In the clinic, patients receive a dose of 250 µg/kg followed by a continuous infusion of 7,5 µg/kg/hour. This is also the dose which we needed in baboons 13, 14 and 15 to obtain full inhibition of the CFRs (final dose of 170420 µg/kg (<figref idref="f0025">figure 30</figref>, table 47). We administered to the baboons a bolus injection only. When a new injury was applied, complete inhibition of the CFRs was retained and infusion of Epinephrin could not reverse this inhibition (<figref idref="f0025">figure 30</figref>).

<u>ALY-0081</u>

0493Nine baboons received ALX-0081 and were used in the Folts model. In all baboons full inhibition of CFRs was obtained at the dose of 30 µg/kg + 45 µg/kg/hour (final dose of 43 µg/kg). In 2 baboons, full inhibition was already obtained at the 10 µg/kg + 15 µg/kg/hour (baboons 17 and 22). Inhibition was retained upon a new injury and after infusion of Epinephrin in all nine baboons (<figref idref="f0026">figure 31</figref>, table 48).

<i>Aspegic-Heparin-Plavix-ALX-0081 (Asp</i>/<i>Hep</i>/<i>Plav</i>/<i>ALX) combinations</i>

0494Seven baboons received a bolus injection of 5 mg/kg Aspirin, 60 IU/kg Heparin and increasing doses of Plavix. Extra Heparin was administered at different time points to sustain a certain level (aPTT should be at least doubled versus control). CFRs were monitored for 30 minutes after each dose of test compounds. We started at a dose of 1 mg/kg Plavix and added 1 mg/kg after 30 minutes. The anti-thrombotic effect was quantified by comparing the length of CFRs before and after drug administration. When full inhibition of CFRs was observed, a new injury was applied. Epinephrin was injected and continued till the end of the experiment. If CFRs did not return, a new injury was applied. After 2-3 CFRs increasing doses of ALX-0081 were added: (1), 3, 10 or 30 µg/kg. We waited after each dose of ALX-0081 for 2 CFRs and increased the dose until full inhibition of CFRs was obtained. At full inhibition of the CFRs, continuous infusion was started of 1,5 times dose ALX-0081/kg/hour for 30 minutes and epinephrine infusion was continued. A new injury was applied after 10-15 minutes. The specifications of the baboons that were used in this study are represented in table 49.

0495The results from these studies for each test compound individually are summarized in table 50. A clear superior anti-thrombotic effect in the Folts thrombosis baboon model is observed for ALX-0081 and Reopro when compared to Aspirin, Heparin or Plavix: upon new injury and after infusion of Epinephrin, the CFRs do not return in the Folts model in the ALX-0081 and Reopro treated baboons in contrast to the model in Aspegic, Heparin or Plavix treated animals. The dose of ALX-0081 required for full inhibition of CFRs is approximately 10-fold lower than the dose needed for Reopro. Therefore, it is concluded that ALX-0081 is more potent than Reopro.

0496After administration of a combination of 5 mg/kg Aspirin, 60 IU/kg Heparin and increasing doses of Plavix, in all seven baboon full inhibition of CFRs was obtained at this final dose. The dose of Plavix required for full inhibition is 2,5-fold lower than the dose needed when Plavix alone is administered. For all baboons tested, CFRs did not return when a new injury was made (<figref idref="f0027">figure 32</figref>). However, upon injection of Epinephrin, CFRs returned spontaneously in baboons 5, 8, 9 and 10 and upon a new injury in baboons 4, 6 and 7. Extra Heparin was injected at the same time as epinephrin. After 2 CFRs, increasing doses of ALX-0081 were administered while continuing the infusion of Epinephrin. The dose of ALX-0081 was increased from 1 over 3-10 to 30 µg/kg. When full inhibition of CFRs was obtained, a continuous infusion of ALX-0081 was started at 1,5 times the effective dose/kg/hour. In all seven baboons, full inhibition of the CFRs was obtained at the 30 µg/kg dose. This effective dose of ALX-0081 is the same as required for complete inhibition of CFRs in the Folts model when ALX-0081 is administered alone.

0497Therefore, we can conclude that the efficacy of ALX-0081 is not increased by simultaneous infusion of Plavix, Heparin and Aspegic. This observation is completely in line with our hypothesis: ALX-0081 inhibits the very first interaction between platelets and the exposed collagen in the damaged arterial wall. Plavix and Aspegic on the other hand inhibit further downstream in the cascade leading to the development of a thrombus. Therefore, Plavix and Aspirin do not contribute to better efficacy as ALX-0081 interferes already with the first step in thrombus formation. Moreover, when a new injury was applied at the effective dose of ALX-0081, the CFRs did not return, demonstrating a potent antithrombotic effect of this Nanobody™. The results are summarized in table 51.

<u>Measurements</u>

0498The following parameters were measured: a) bleeding analysis, b) vWF concentration, Factor VIII levels, and platelet count, PT and aPTT c) ristocetin-induced platelet aggregation d) ALX-0081 concentration, and e) analysis of arterial sections for restenosis, f) immunogenicity of ALX-0081

a) Bleeding analysis

0499To analyze bleeding, an incision was made with a scalpel in the groin. This was done at 15 minutes after recording baseline flow, when the injury was made in the artery. Gauzes were inserted in the wound and replaced every 30 minutes just before each new dose of test compound. The amount of blood loss after each dose of test compound was determined by weighing the gauzes. Blood loss is expressed relative to the amount of blood loss in the second control gauze (during the saline injection) (tables 52-54).

0500For all baboons treated with Plavix and Reopro, blood loss is high (up to 9-40 fold respectively at the highest dose), starting from the effective dose on. For animals treated with ALX-0081 bleeding is lower than in the Plavix treated animals, and much lower when compared to Reopro treated animals.

0501In order to determine the safety versus efficacy level of Plavix, Reopro and ALX-0081 as antithrombotic drugs, the averages of blood loss relative to the second control gauze are shown for these drugs in function of the drug dose as multiple of the effective dose (<figref idref="f0028">figure 33</figref>). The effective dose for Plavix is 5 mg/kg, for Reopro 250 µg/kg and for ALX-0081 30 µg/kg (table 46-48). These results nicely demonstrate the superior safety of ALX-0081 when compared to Reopro and Plavix: the window in which ALX-0081 could be administered without a major increase in bleeding is much wider compared to Plavix and Reopro.

0502The results from the averages of blood loss in the gauzes (if available) were combined with the averages of the lengths of the CFRs in the <figref idref="f0029 f0031">figures 34-36</figref>.

0503A broad therapeutic window was observed for ALX-0081 in the Folts model: a strong antithrombotic effect could be demonstrated without any major bleedings for cumulative doses ranging from 43 µg/kg up to 403 µg/kg (<figref idref="f0031">figure 36</figref>). In contrast however, the therapeutic window for Reopro and Plavix in the same model was much more narrow compared to ALX-0081, combining an effective antithrombotic effect with a high blood loss (<figref idref="f0029 f0030">figure 34-35</figref>).

0504The average of the total amount of blood loss (= sum of blood loss from the gauzes of the first five doses of test compound) as relative to the second control gauze are summarized in table 55. In this table we also indicate the final dose as multiple of the effective dose (= sum of the five doses divided by the effective dose). As mentioned before, the effective dose for Plavix is 5 mg/kg, for Reopro 250 µg/kg and for ALX-0081 30 µg/kg.

0505The results shown in table 55 clearly show that total blood loss is significantly increased in the animals treated with Plavix and to an even higher extent in the animals treated with Reopro. Blood loss in animals receiving ALX-0081 is 2-fold and 4 fold less than in Plavix or Reopro treated animals, respectively. This again clearly demonstrates that ALX-0081 is safer than Plavix and Reopro in terms of bleeding risk, although doses of more than 10-fold the effective dose were used.

0506The effective combination of Aspegic, Heparin and Plavix results in an increase in blood loss of up to 14 fold when compared to the control gauze (table 56). Addition of ALX-0081 on top of the combination of Aspegic, Heparin and Plavix does not result in increased bleeding except for baboons 4 and 7. In baboon 7, bleeding was much increased after administration of epinephrine, extra heparin and non effective doses of ALX-0081, but was lower again after administration of the effective dose of ALX-0081. These results demonstrated that ALX-0081 is safe when added on top of the combination of drugs that is currently used in a clinical setting.

b) vWF concentration. Factor VIII level, platelet count, PT and aPTT

<u>vWF</u>

0507The vWF levels in the platelet rich plasma (PRP) of blood samples taken after administration of the different doses of the drugs in the Folts model were determined using an immunosorbent assay and expressed as a percentage of the human standard (WHO 5^th International Standard for factor VIII and VWF)

0508The results clearly demonstrate that the different drugs used in the model have no major effect on the vWF level.

<u>Factor VIII</u>

0509The factor VIII levels in the PRP of blood samples taken after administration of the different doses of the drugs in the Folts model were determined using the aPTT test. We did not test the plasma samples of the baboons treated with Heparin, as we demonstrated that Heparin prolongs the aPTT time. The FVIII levels were expressed as percentage of the first control sample, taken 10 minutes after injury of the femoral artery. We do not see any effect of the treatments on the aPTT test.

<u>Platelet count, PT and aPTT</u>

0510The platelet count measurements during the Folts model experiments were performed. The data showed that baboon 15 has a very low platelet count when compared to the other animals. The platelet counts for all kind of treatments, except for the Plavix treatment, are very comparable to what we see in the control animals and are fairly constant over time.

0511The PT values demonstrate no effect of the test compounds on the PT time, except for baboons treated with the 240 IU/kg dose of Heparin where a minor increase in PT was observed.

0512The aPTT values observed during the Folts model studies are summarized. These results indicate that the test compounds have no effect on the aPTT values, except for the baboons treated with Heparin. In these animals, aPTT values are prolonged from the 30-60 IU/kg dose on, as is also observed in patients. Heparin acts as an anticoagulant by forming a complex with antithrombin and catalyzing the inhibition of activated blood coagulation factors such as XIa, IXa, Xa and thrombin (factor IIa). These factors are all involved in the intrinsic coagulation cascade of which its functionality is measured in the aPTT test.

c) Measurement of ristocetin-induced platelet aggregation in blood obtained from baboons treated with ALX-0081

0513Blood obtained from baboons treated with ALX-0081 was analyzed for inhibition of platelet aggregation. Platelet aggregations were performed on a Chronolog whole blood and optical Aggregometer (Model 560CA, Chronolog, USA). PRP was prepared (collected on 0.38 mol/L citrate), by centrifuging the whole blood at 1200 rpm for 5 minutes. The upper fraction containing the PRP was carefully removed. The lower fraction was further centrifuged at 3000 rpm for 10 minutes to prepare platelet poor plasma (PPP). Platelets were counted in PRP and diluted in PPP to a final concentration of 200.000 platelets per microliter. 3 mg/ml ristocetin (DAKO) was added and aggregation was measured.

0514The <i>ex vivo</i> platelet aggregation is measured in the blood samples taken during the Folts experiment in the baboons treated with ALX-0081. The GPIb-IX-V dependent platelet aggregation through vWF is measured using ristocetin as a modulator. The % aggregation is measured at each time point and at each dose. The control sample is taken at 10 minutes after arterial injury.

0515Results from the RIPA test are compared to the inhibition of the CFRs for each baboon treated with ALX-0081 (<figref idref="f0032 f0033 f0034 f0035 f0036">figure 37</figref>). As shown in <figref idref="f0032 f0033 f0034 f0035 f0036">figure 37</figref>, an inverse relation between the RIPA and the length of the CFRs is observed. Moreover, these results demonstrate that full inhibition in the RIPA test is obtained at lower doses than full inhibition of CFRs in baboons 16, 18, 19 and 23. For baboons 20, 21, 22 and 24 the results with RIPA compare very well with the results for efficacy in the Folts model.

d) Concentration of ALX-0081

0516Microtiterplates are coated with mouse polyclonal anti-myc overnight at 4°C at a 1000-fold dilution. The plates are washed with PBS-Tween and blocked for 2 hours at RT with PBS-1% casein. Samples are diluted in a non-coated microtiterplate in 25% reference baboon plasma. The standard curve is prepared by diluting the nanobody in the same reference baboon plasma sample. Samples are applied on the anti-myc coated plates and allowed to bind for 2 hours at RT. The plates are washed 5 times with PBS-Tween. Rabbit anti-vWF-HRP (DAKO) is applied at a 3000-fold dilution for one hour at RT. For measuring OD405 nm, samples are washed 5 times with PBS-Tween and ABTS/H₂O₂ substrate is added.

0517We determined the concentration of ALX-0081 in plasma samples taken at 10 minutes after each bolus injection. The bolus injection was immediately followed by a continuous infusion. The concentrations (µg/ml) are summarized in table 58.

0518For all baboons an increasing level of ALX-0081 in the plasma samples was measured by ELISA after dose-escalation of ALX-0081. For baboon 16, consistently higher amounts of ALX-0081 were determined in the plasma sample taken after the 10 µg/kg dose compared to the sample taken after 30 µg/kg. The ALX-0081 level in that sample is also substantially higher than what is noted for all other baboons given the same dosing schedule of ALX-0081. As the levels of ALX-0081 for baboon 16 after the higher doses are in line of the expectations, we assume that an unknown abnormality during blood sampling accounts for this outlier.

0519The concentration of ALX-0081 for each dose in the different baboons is variable. For the 3 µg/kg dose, the concentration ranges between 0,03 and 0,14 µg/ml for 10 µg/kg between 0,18 and 1,23 µg/ml, for 30 µg/kg between 0,51 and 1,14 µg/ml, for 90 µg/kg between 1,38 and 6,77 µg/ml and for 270 µg/kg between 4,03 and 35,14 µg/ml. In <figref idref="f0037">figure 38</figref>, we plot the concentration of ALX-0081 in plasma versus the length of the CFRs.

0520The concentration of ALX-0081 required for full inhibition of CFRs is between 0,3 and 0,5 µg/ml, which is in full agreement with the concentration required to inhibit platelet adhesion to collagen in the flow chamber at high shear rate, when ALX-0081 is spiked in human blood. In blue (<figref idref="f0037">figure 38</figref>, panel B) we indicated the concentration range of ALX-0081 where inhibition starts (leaving out the 10 µg/kg dose in baboon 16).

0521When we plot the concentration of ALX-0081 versus the relative amount of blood loss from the gauzes, we observe a more than 2-fold increase in bleeding at doses above 1 µg/ml (<figref idref="f0038">figure 39</figref>). A 10-fold increase in blood loss was observed when the ALX-0081 concentration is 19 µg/ml, which is 40-60-fold the effective concentration.

e) Analysis of arterial sections for restenosis

0522Four weeks after treatment of the second artery, the arteries are dissected free from surrounding tissue. The artery is tied at the upper and low site of the endothelial injury including the site where the shunt was placed. A section is removed of 2 centimetre, cut in a lower (shunt site) and upper part (stenosed and injured site) and stored in 10% formaldehyde. The baboons are then sacrificed by euthanase injection. The arteries are marked according to origin and cut into rings of 2 mm each. The rings are placed into marked cassettes suitable for histology processing. The cassettes are then placed overnight in an automated VIP Tissue Tek processor following the overnight processing schedule as described in Bancroft (<nplcit id="ncit0136" npl-type="b"><text>Bancroft, John D., Stevens Alan (1990). Theory and Practice of Histological Techniques. Third Editi</text></nplcit>on).

0523After processing, the arteries are embedded in marked paraffin wax blocks and cooled on a freeze plate. The wax blocks are cut in series sections of 4 micron each on a rotary microtome. Sections are picked up on glass slides and stained for histological evaluation. Haematoxylin and Eosin as well as Verhoeff's method for elastic fibers stains are performed on each of the arteries (<nplcit id="ncit0137" npl-type="b"><text>Bancroft, John D., Stevens Alan (1990). Theory and Practice of Histological Techniques. Third Editi</text></nplcit>on). After staining, the slides are dehydrated, cleared, mounted and labelled. Blind analysis of the sections is performed.

f) Immunogenicity analysis

0524The presence of ALX-0081 immunoglobulins in plasma of three baboons was evaluated by two methods, respectively an ELISA method and a SPR-based method on Biacore. The baboons were treated for 8 weeks with increasing doses of ALX-0081 (starting from 10 µg/kg). During said 8 weeks, no immunogenic response could be observed upon injection of ALX-0081. The half-life of ALX-0081 ranged between 7 and 9 hours.

Example 20: Use of vWF as an antidote for ALX-0081

0525Despite the proven safety of ALX-0081 in baboons, and the rapid clearance of the Nanobody™, we decided to evaluate the use of vWF as an antidote for ALX-0081. This was tested in a Folts model in baboons where we evaluated if the inhibitory effect of ALX-0081 on arterial thrombus formation can be reversed by injection of vWF.

0526The experimental procedure followed the original Folts model with the modifications as described in the previous example 18.

0527Healthy male baboons (<i>Papio ursinus</i>) were used in this study. The animals were 9-12 kg of weight and were disease-free for at least 2 weeks prior to use. The baboons were fed with dry standard food only.

0528Three baboons were used in this study, the length of the CFRs during the control phase, after administration saline, ALX-0081 and vWF is summarized in table 59.

0529The blood flow as a function of time for each baboon and experiment is shown in <figref idref="f0039">figure 40</figref>.

0530In all three baboons, full inhibition of CFRs was obtained at the 30 µg/kg + 45 µg/kg/hour dose of ALX-0081, even when a new injury was applied, the CFRs did not return. Upon injection of the first dose of vWF (250 IU), the flow gradually decreased, but CFRs did not return until an extra dose of 250 IU of vWF was administered. This result demonstrated nicely that the activity of ALX-0081 can be reversed by administration of vWF, and that therefore, vWF would be a good antidote for this Nanobody™.

0531Thus, another aspect of the invention relates to the use of vWF, of a suitable fragment thereof, of DDAVP (desmopressinor) or a suitable fragment thereof, or of a pharmaceutical composition comprising any of the foregoing, as an antidote for complications or undesired side effects associated with the use of a Nanobody, protein or polypeptide against vWF, in particular a Nanobody, protein or polypeptide as described herein.

Example 21: Effects of ALX-0081 on platelet adhesion to endothelial cell-derived UlvWF and on the activity of ADAMTS-13

0532This study serves as a proof of concept for the use of ALX-0081 as a drug in TTP patients. Perfusions of platelets reconstituted in TTP plasma (no ADAMTS13) are performed on endothelial cells secreting ULvWF, in the absence and presence of ALX-0081. In a separate experiment we test if ALX-0081, which binds to the A1 domain of vWF, interferes with the ADAMTS-13 activity. ADAMTS-13 binds to and cleaves the A2 domain of vWF.

0533Endothelial cells were obtained from human umbilical cord veins by the method of <nplcit id="ncit0138" npl-type="s"><text>Maruyama (Z.Zellforsch. Mikrosk. A4nat. 60:69; 1963</text></nplcit>). Endothelial cells were activated with 100 µM histamine (Sigma-Aldrich, St Louis, MO) for 15 minutes at room temperature before the perfusion experiments.

0534Blood was drawn from healthy volunteers who denied ingestion of aspirin or other nonsteroidal anti-inflammatory drugs (NSAIDs) for the preceding 10 days into one-tenth volume 3.4% sodium citrate. Platelet-rich plasma (PRP) was prepared from whole blood by centrifugation (10 minutes at 200g at room temperature). The PRP was acidified by addition of one-tenth volume of ACD (2.5% trisodium citrate, 1.5% citric acid, and 2% D-glucose), and the platelets were spun down (500g, 15 minutes). The platelet pellet was resuspended in HEPES (N-2-hydroxyethylpiperdzine-N'-2-ethanesulfonic acid)-Tyrode buffer (10 mM HEPES, 137 mM NaCl, 2.68 mM KCl, 0.42 mM NaH₂PO₄, 1.7 mM MgCl₂, 5 mM D-glucose, pH 6.5). Prostacyclin (PGI₂, 10 ng/mL) was added to prevent platelet activation during the subsequent washing step. Platelets were spun down and resuspended in a small volume of HEPES-Tyrode buffer. This platelet suspension was diluted in HEPES buffer at pH 7.4, or in TTP plasma.

0535Perfusions were performed in a single-pass perfusion chamber as described previously. The experiment was followed by real-time videomicroscopy.

0536In a second type of experiment, different reaction mixtures were prepared as summarized in table 60, however, without the addition of the A1A2A3 construct. The A1A2A3 construct is a recombinant fragment consisting out of the A1, A2 and A3 domain of vWF. Mixtures were pre-incubated for 5 minutes at 37°C after which the A1A2A3 fragment is added and the mixture is incubated in a waterbath overnight at 37°C. The next day a reducing SDS-PAGE is run on the samples (12%, and using as marker the Precision Plus Protein Standards from BioRad) and blotted on Immobilon-FL (Millipore). The blot was blocked for 2 hours at room temperature with blockbuffer (1:1 Odyssey blockbuffer in 1xTBS pH=7,4) and incubated with Rabbit polyclonal anti-vWF (DAKO). Alexa Fluor 680 goat anti-rabbit was used for detection. Scanning was done on the ODYSSEY to detect the degradation products.

<i>Control experiment: binding of platelets to ULvWF</i>

0537Endothelial cells were isolated from freshly obtained human umbilical cords by collagenase digestion of the interior of the umbilical vein. The cells were grown in tissue culture as a homogeneous population. Cultured human endothelial cells grow as monolayers of closely opposed, polygonal large cells and they contain cytoplasmic inclusions (Weibel-Palade bodies). Histamine-stimulated endothelial cells isolated from human umbilical cords express ultra-large von Willebrand factor (ULvWF) on their surface. Perfusion of these stimulated cells with isolated blood platelets, which are suspended into either buffer or plasma from a patient with aquired TTP, results in deposition of platelets onto the ULvWF (8). These ULvWF-adhered platelets appear as so-called 'strings', which are visible when the perfusion experiment is monitored by real-time video microscopy (<figref idref="f0040">figure 41</figref>).

<i>Inhibition by ALX-0081 for the generation of platelet strings</i>

0538Platelets were resuspended in buffer or in TTP plasma and the concentrations of ALX-0081 used in this experiment were 0,2, 2 and 10 µg/ml. Histamine-stimulated endothelial cells isolated from human umbilical cords are perfused with these platelet suspensions as described above.

0539Addition of ALX-0081 to platelets resuspended in buffer or in plasma from a TTP patient results in a complete inhibition of string formation under all conditions tested (<figref idref="f0040">figure 42</figref>). Perfusion experiments were performed at a shear stress of 2.5 dyn/cm2 for 4 minutes. During this 4 minute perfusion at least 20 microscopic fields were examined, and in the presence of the Nanobody™, no strings could be demonstrated at all conditions tested (<figref idref="f0040">figure 42</figref>).

<i>Cleavage of ULvWF by ADAMTS-13</i>

0540ADAMTS-13 reduces the size of large and ultralarge VWF multimers to smaller forms by specifically cleaving the Y842/M843 peptide bond in the VWF A2 domain. Two types of assays were used to evaluate the effect of ALX-0081 on the cleavage of ULvWF by ADAMTS-13: i.e. a perfusion assay and an assay observing the cleavage of a recombinant vWF fragment. In a first experiment, strings were generated by a 4 minute perfusion of washed platelets resuspended in buffer over histamine-stimulated endothelial cells. Subsequently, the non-adhered platelets were washed away by a 4 minute perfusion of buffer. After that, buffer was perfused for an other 4 minutes, followed by a 4 minute perfusion of pooled normal plasma containing ADAMTS-13. Detachment of the platelet strings was observed after perfusion of pooled normal plasma (<figref idref="f0040">figure 43</figref>). More than 95% of the strings were cleaved after the 4 minute perfusion.

0541In a next experiment, strings were generated by a 4 minute perfusion of washed platelets resuspended in buffer over histamine-stimulated endothelial cells and the non-adhered platelets were washed away by a 4 minute perfusion of buffer as above. After that, ALX-0081 (10 µg/ml in buffer) was perfused for 4 minutes, followed by a 4 minute perfusion of pooled normal plasma containing ALX-0081 (10 µg/ml= 10-fold molar excess over vWF) and ADAMTS-13. We could clearly demonstrate detachment of the platelet strings and 95% of the strings were cleaved after the 4 minute perfusion (<figref idref="f0041">figure 44</figref>)

0542These results clearly demonstrate that ALX-0081 does not have an effect on the cleavage of ULvWF strings by ADAMTS-13.

0543In a second assay, a recombinant fragment containing the A1-A2-A3 domain of vWF was mixed with normal pool plasma (NPP) containing ADAMTS-13, resulting in proteolytic cleavage of the fragment which was observed by a Western Blot analysis. ADAMTS-13 activity was tested in the absence and presence of 10 µg/ml ALX-0081. As indicated in figure 45 ALX-0081 has no effect on the cleavage of the vWF fragment (lanes 6-7-8).

0544In order to demonstrate that the observed cleavage is specific for ADAMTS-13, a control experiment in the presence of EDTA was performed as EDTA inhibits the activity of ADAMTS-13. As expected, the presence of EDTA in NPP resulted in inhibition of cleavage of the fragment (figure 451ane 4).

0545This experiment again proves that ALX-0081 has no effect on the ADAMTS-13 activity. <tables id="tabl0034" num="0034"><table frame="all"><title><u>Table 8:</u> Sequence listing of anti-vWF nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="15mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="123mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>60</entry><entry><img file="EP3415535A1_D0122.tif" /></entry></row><row><entry>12B1</entry><entry>61</entry><entry><img file="EP3415535A1_D0123.tif" /></entry></row><row><entry>12B6</entry><entry>62</entry><entry><img file="EP3415535A1_D0124.tif" /></entry></row><row><entry>12D11</entry><entry>63</entry><entry><img file="EP3415535A1_D0125.tif" /></entry></row><row><entry>12E3</entry><entry>64</entry><entry><img file="EP3415535A1_D0126.tif" /></entry></row><row><entry>12C9</entry><entry>65</entry><entry><img file="EP3415535A1_D0127.tif" /></entry></row><row><entry>14F8</entry><entry>66</entry><entry><img file="EP3415535A1_D0128.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0035" num="0035"><table frame="all"><title><u>Table 9:</u> Expression yields of anti-vWF nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="37mm" /><colspec colnum="2" colname="col2" colwidth="42mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Yield (mg/l) after TALON</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>13</entry></row><row><entry>12B1</entry><entry>6</entry></row><row><entry>12B6</entry><entry>16</entry></row><row><entry>12D11</entry><entry>8</entry></row><row><entry>12E3</entry><entry>4</entry></row><row><entry>12C9</entry><entry>25</entry></row><row><entry>14F8)</entry><entry>48</entry></row></tbody></tgroup></table></tables><tables id="tabl0036" num="0036"><table frame="all"><title><u>Table 10:</u> Platelet adhesion in perfusion chamber of anti-vWF nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="35mm" /><colspec colnum="2" colname="col2" colwidth="34mm" /><colspec colnum="3" colname="col3" colwidth="49mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Control</b></entry><entry valign="top"><b>% Platelet adhesion at 2 µg/ml</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>60 ± 7</entry><entry>10 ± 3</entry></row><row><entry>12B1</entry><entry>60 ± 7</entry><entry>56 ± 3</entry></row><row><entry>12B6</entry><entry>60 ± 7</entry><entry>19 ± 5</entry></row><row><entry>12D11</entry><entry>60 ± 7</entry><entry>61 ± 7</entry></row><row><entry>12E3</entry><entry>60 ± 7</entry><entry>54 ± 1</entry></row><row><entry>12C9</entry><entry>71 ± 3</entry><entry>68 ± 8</entry></row><row><entry>14F8</entry><entry>71 ± 3</entry><entry>51 ± 10</entry></row></tbody></tgroup></table></tables><tables id="tabl0037" num="0037"><table frame="all"><title><u>Table 11:</u> Sequence listing of 12B6 and 12A5 homologue nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="15mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="122mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row><row><entry namest="col1" nameend="col3" align="left" valign="top"><b>12A5 homologue sequences</b></entry></row></thead><tbody><row><entry>12B4</entry><entry>67</entry><entry><img file="EP3415535A1_D0129.tif" /></entry></row><row><entry>12E8</entry><entry>68</entry><entry><img file="EP3415535A1_D0130.tif" /></entry></row><row><entry>12A6</entry><entry>69</entry><entry><img file="EP3415535A1_D0131.tif" /></entry></row><row><entry>12D8</entry><entry>70</entry><entry><img file="EP3415535A1_D0132.tif" /></entry></row></tbody></tgroup><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="15mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="122mm" /><thead><row><entry namest="col1" nameend="col3" align="left" valign="top"><b>12B6 homologue sequences</b></entry></row></thead><tbody><row><entry>12A2</entry><entry>71</entry><entry><img file="EP3415535A1_D0133.tif" /></entry></row><row><entry>12F2</entry><entry>72</entry><entry><img file="EP3415535A1_D0134.tif" /></entry></row><row><entry>14H10</entry><entry>73</entry><entry><img file="EP3415535A1_D0135.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0038" num="0038"><table frame="all"><title><u>Table 12:</u> Estimated K-on, K-off and KD values for 12A5 homologue nanobodies</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="31mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><colspec colnum="4" colname="col4" colwidth="25mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Koff (x10^-3/s)</b></entry><entry valign="top"><b>Kon (x 10⁶ 1/Ms)</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>2.51</entry><entry>0.629</entry><entry>3.98</entry></row><row><entry>12B4</entry><entry>2.2</entry><entry>0.544</entry><entry>4.05</entry></row><row><entry>12E8</entry><entry>2.93</entry><entry>0.171</entry><entry>17.1</entry></row><row><entry>12A6</entry><entry>4.72</entry><entry>0.188</entry><entry>25.1</entry></row><row><entry>12D8</entry><entry>5.84</entry><entry>0.139</entry><entry>41.9</entry></row></tbody></tgroup></table></tables><tables id="tabl0039" num="0039"><table frame="all"><title><u>Table 13:</u> Estimated K-on, K-off and KD values for 12B6 homologue nanobodies</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="31mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><colspec colnum="4" colname="col4" colwidth="25mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Koff (x10^-3/s)</b></entry><entry valign="top"><b>Kon (x 10⁶ 1/Ms)</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>5.97</entry><entry>2.55</entry><entry>2.33</entry></row><row><entry>12A2</entry><entry>3.49</entry><entry>1.11</entry><entry>3.13</entry></row><row><entry>12F2</entry><entry>4.04</entry><entry>6.41</entry><entry>6.3</entry></row><row><entry>14H10</entry><entry>3.97</entry><entry>6.84</entry><entry>5.81</entry></row></tbody></tgroup></table></tables><tables id="tabl0040" num="0040"><table frame="all"><title><u>Table 14:</u> Real KD value of 12B6, 12A2 and 12A5 nanobodies</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="27mm" /><colspec colnum="2" colname="col2" colwidth="24mm" /><colspec colnum="3" colname="col3" colwidth="29mm" /><colspec colnum="4" colname="col4" colwidth="19mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Koff (x10^-3/s)</b></entry><entry valign="top"><b>Kon (x 10⁶ 1/Ms)</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>10.03</entry><entry>2.28</entry><entry>4.5</entry></row><row><entry>12A2</entry><entry>9.9</entry><entry>2.24</entry><entry>4.4</entry></row><row><entry>12A5</entry><entry>3.3</entry><entry>1.22</entry><entry>2.7</entry></row></tbody></tgroup></table></tables><tables id="tabl0041" num="0041"><table frame="all"><title><u>Table</u> 15: Platelet adhesion in perfusion chamber of 12B6, 12A2 and 12A5 nanobodies</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="30mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><colspec colnum="3" colname="col3" colwidth="23mm" /><colspec colnum="4" colname="col4" colwidth="23mm" /><colspec colnum="5" colname="col5" colwidth="23mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col5" align="left" valign="top"><b>% Platelet adhesion</b></entry></row><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>0 µg/ml</b></entry><entry valign="top"><b>0.2 µg/ml</b></entry><entry valign="top"><b>0.4 µg/ml</b></entry><entry valign="top"><b>0.6 µg/ml</b></entry></row></thead><tbody><row><entry>Control</entry><entry>71 ± 3</entry><entry>-</entry><entry>-</entry><entry>-</entry></row><row><entry>12B6</entry><entry>-</entry><entry>59 ± 6</entry><entry>43 ± 7</entry><entry>27 ± 6</entry></row><row><entry>12A2</entry><entry>-</entry><entry>56 ± 8</entry><entry>40 ± 10</entry><entry>11 ± 8</entry></row><row><entry>12A5</entry><entry>-</entry><entry>50 ± 7</entry><entry>27 ± 10</entry><entry>2 ± 2</entry></row></tbody></tgroup></table></tables><tables id="tabl0042" num="0042"><table frame="all"><title><u>Table 16:</u> Concentration of 12B6, 12A2 and 12A5 nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="26mm" /><colspec colnum="2" colname="col2" colwidth="16mm" /><colspec colnum="3" colname="col3" colwidth="18mm" /><colspec colnum="4" colname="col4" colwidth="18mm" /><colspec colnum="5" colname="col5" colwidth="18mm" /><colspec colnum="6" colname="col6" colwidth="18mm" /><colspec colnum="7" colname="col7" colwidth="18mm" /><colspec colnum="8" colname="col8" colwidth="18mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>100</entry><entry>97</entry><entry>100</entry><entry>104</entry><entry>94</entry><entry>91</entry><entry>68</entry></row><row><entry>12A2</entry><entry>100</entry><entry>106</entry><entry>104</entry><entry>100</entry><entry>93</entry><entry>87</entry><entry>90</entry></row><row><entry>12A5</entry><entry>100</entry><entry>108</entry><entry>107</entry><entry>98</entry><entry>83</entry><entry>75</entry><entry>66</entry></row></tbody></tgroup></table></tables><tables id="tabl0043" num="0043"><table frame="all"><title><u>Table 17:</u> Sequence listing of bivalent nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="31mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="105mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12A2-3a-12A2</entry><entry>74</entry><entry><img file="EP3415535A1_D0136.tif" /></entry></row><row><entry>12A2-GS9-12A2</entry><entry>75</entry><entry><img file="EP3415535A1_D0137.tif" /></entry></row><row><entry>12A2-GS30-12A2</entry><entry>76</entry><entry><img file="EP3415535A1_D0138.tif" /></entry></row><row><entry>12A5-3a-12A5</entry><entry>77</entry><entry><img file="EP3415535A1_D0139.tif" /></entry></row><row><entry>12A5-GS9-12A5</entry><entry>78</entry><entry><img file="EP3415535A1_D0140.tif" /></entry></row><row><entry>12A5-GS30-12A5</entry><entry>79</entry><entry><img file="EP3415535A1_D0141.tif" /></entry></row><row><entry>12B6-3e-12B6</entry><entry>60</entry><entry><img file="EP3415535A1_D0142.tif" /></entry></row><row><entry>12B6-GS9-12B6</entry><entry>81</entry><entry><img file="EP3415535A1_D0143.tif" /></entry></row><row><entry>12B6-GS30-12B6</entry><entry>82</entry><entry><img file="EP3415535A1_D0144.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0044" num="0044"><table frame="all"><title><u>Table 18</u>: Sequence listing of linker sequences</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="14mm" /><colspec colnum="2" colname="col2" colwidth="20mm" /><colspec colnum="3" colname="col3" colwidth="78mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>3a</entry><entry>83</entry><entry>AAA</entry></row><row><entry>GS9</entry><entry>84</entry><entry>GGGGSGGGS</entry></row><row><entry>GS30</entry><entry>85</entry><entry>GGGGSGGGGSGGGGSGGGGSGGGGSGGGGS</entry></row></tbody></tgroup></table></tables><tables id="tabl0045" num="0045"><table frame="all"><title><u>Table 19:</u> Expression yields of bivalent 12B6, 12A2 and 12A5 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="52mm" /><colspec colnum="2" colname="col2" colwidth="70mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Yield (mg/l) after TALON or other purification</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>16</entry></row><row><entry>12B6-3a-12B6</entry><entry>9</entry></row><row><entry>12B6-GS9-12B6</entry><entry>16</entry></row><row><entry>12B6-GS30-12B6</entry><entry>17</entry></row><row><entry>12A2</entry><entry>18</entry></row><row><entry>12A2-3a-12A2</entry><entry>45</entry></row><row><entry>12A2-GS9-12A2</entry><entry>22</entry></row><row><entry>12A2-GS30-12A2</entry><entry>11</entry></row><row><entry>12A5</entry><entry>13</entry></row><row><entry>12A5-3a-12A5</entry><entry>10</entry></row><row><entry>12A5-GS9-12A5</entry><entry>11</entry></row><row><entry>12A5-GS30-12A5</entry><entry>18</entry></row></tbody></tgroup></table></tables><tables id="tabl0046" num="0046"><table frame="all"><title><u>Table 20:</u> Concentration of 12B6 bivalent nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="31mm" /><colspec colnum="2" colname="col2" colwidth="14mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="16mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="16mm" /><colspec colnum="7" colname="col7" colwidth="16mm" /><colspec colnum="8" colname="col8" colwidth="16mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>100</entry><entry>97</entry><entry>100</entry><entry>104</entry><entry>94</entry><entry>91</entry><entry>68</entry></row><row><entry>12B6-3a-12B6</entry><entry>100</entry><entry>103</entry><entry>96</entry><entry>87</entry><entry>9</entry><entry>8</entry><entry>6</entry></row><row><entry>12B6-GS9-12B6</entry><entry>100</entry><entry>103</entry><entry>94</entry><entry>88</entry><entry>19</entry><entry>8</entry><entry>7</entry></row><row><entry>12B6-GS30-12B6</entry><entry>100</entry><entry>100</entry><entry>100</entry><entry>98</entry><entry>46</entry><entry>14</entry><entry>11</entry></row></tbody></tgroup></table></tables><tables id="tabl0047" num="0047"><table frame="all"><title><u>Table 21:</u> Concentration of 12A2 bivalent nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="31mm" /><colspec colnum="2" colname="col2" colwidth="14mm" /><colspec colnum="3" colname="col3" colwidth="15mm" /><colspec colnum="4" colname="col4" colwidth="15mm" /><colspec colnum="5" colname="col5" colwidth="15mm" /><colspec colnum="6" colname="col6" colwidth="15mm" /><colspec colnum="7" colname="col7" colwidth="15mm" /><colspec colnum="8" colname="col8" colwidth="15mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°6</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>66°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12A2</entry><entry>100</entry><entry>106</entry><entry>104</entry><entry>100</entry><entry>93</entry><entry>87</entry><entry>90</entry></row><row><entry>12A2-3a-12A2</entry><entry>100</entry><entry>87</entry><entry>88</entry><entry>91</entry><entry>55</entry><entry>50</entry><entry>43</entry></row><row><entry>12A2-6S9-12A2</entry><entry>100</entry><entry>102</entry><entry>113</entry><entry>138</entry><entry>91</entry><entry>113</entry><entry>15</entry></row><row><entry>12A2-GS30-12A2</entry><entry>100</entry><entry>115</entry><entry>93</entry><entry>116</entry><entry>81</entry><entry>49</entry><entry>34</entry></row></tbody></tgroup></table></tables><tables id="tabl0048" num="0048"><table frame="all"><title><u>Table 22:</u> Concentration of 12A5 bivalent nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="31mm" /><colspec colnum="2" colname="col2" colwidth="14mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="16mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="16mm" /><colspec colnum="7" colname="col7" colwidth="16mm" /><colspec colnum="8" colname="col8" colwidth="16mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>100</entry><entry>108</entry><entry>107</entry><entry>98</entry><entry>83</entry><entry>75</entry><entry>66</entry></row><row><entry>12A5-3a-12A5</entry><entry>100</entry><entry>101</entry><entry>114</entry><entry>29</entry><entry>6</entry><entry>4</entry><entry>6</entry></row><row><entry>12A5-GS9-12A5</entry><entry>100</entry><entry>104</entry><entry>115</entry><entry>32</entry><entry>13</entry><entry>14</entry><entry>10</entry></row><row><entry>12A5-GS30-12A5</entry><entry>100</entry><entry>104</entry><entry>87</entry><entry>7</entry><entry>6</entry><entry>35</entry><entry>21</entry></row></tbody></tgroup></table></tables><tables id="tabl0049" num="0049"><table frame="all"><title>Table 23: Platelet adhesion in perfusion chamber of 12A2 bivalent nanobodies</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="31mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="21mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col5" align="left" valign="top"><b>% Platelet adhesion</b></entry></row><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>0 µg/ml</b></entry><entry valign="top"><b>0.1 µg/ml</b></entry><entry valign="top"><b>0.2 µg/ml</b></entry><entry valign="top"><b>0.4 µg/ml</b></entry></row></thead><tbody><row><entry>Control</entry><entry>81±5</entry><entry>-</entry><entry>-</entry><entry>-</entry></row><row><entry>12A2</entry><entry>-</entry><entry>78±2</entry><entry>72±6</entry><entry>61±8</entry></row><row><entry>12A2-3a-12A2</entry><entry>-</entry><entry>74+5</entry><entry>50±3</entry><entry>33±0</entry></row><row><entry>12A2-GS9-12A2</entry><entry>-</entry><entry>81±1</entry><entry>73±1</entry><entry>40±2</entry></row><row><entry>12A2-GS30-12A2</entry><entry>-</entry><entry>81±3</entry><entry>73±3</entry><entry>37±1</entry></row></tbody></tgroup></table></tables><tables id="tabl0050" num="0050"><table frame="all"><title><u>Table 24:</u> Sequence listing of humanised 12B6 nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="122mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12B6H1</entry><entry>86</entry><entry><img file="EP3415535A1_D0145.tif" /></entry></row><row><entry>12B6H2</entry><entry>87</entry><entry><img file="EP3415535A1_D0146.tif" /></entry></row><row><entry>12B6H3</entry><entry>88</entry><entry><img file="EP3415535A1_D0147.tif" /></entry></row><row><entry>12B6H4</entry><entry>89</entry><entry><img file="EP3415535A1_D0148.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0051" num="0051"><table frame="all"><title><u>Table 25:</u> Expression yields of wild type and humanised 12B6 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="52mm" /><colspec colnum="2" colname="col2" colwidth="72mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Yield (mg/l) after TALON or other purification</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>16</entry></row><row><entry>12B6H1</entry><entry>3</entry></row><row><entry>12B6H2</entry><entry>9</entry></row><row><entry>12B6H3</entry><entry>8</entry></row><row><entry>12B6H4</entry><entry>13</entry></row></tbody></tgroup></table></tables><tables id="tabl0052" num="0052"><table frame="all"><title><u>Table 26:</u> Concentration of wild type and humanised 12B6 nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="28mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><colspec colnum="3" colname="col3" colwidth="19mm" /><colspec colnum="4" colname="col4" colwidth="19mm" /><colspec colnum="5" colname="col5" colwidth="19mm" /><colspec colnum="6" colname="col6" colwidth="19mm" /><colspec colnum="7" colname="col7" colwidth="19mm" /><colspec colnum="8" colname="col8" colwidth="19mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>56°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>100</entry><entry>97</entry><entry>100</entry><entry>104</entry><entry>94</entry><entry>91</entry><entry>68</entry></row><row><entry>12B6H1</entry><entry>100</entry><entry>101</entry><entry>100</entry><entry>97</entry><entry>146</entry><entry>56</entry><entry>54</entry></row><row><entry>12BSH2</entry><entry>100</entry><entry>97</entry><entry>96</entry><entry>96</entry><entry>83</entry><entry>46</entry><entry>53</entry></row><row><entry>12B6H3</entry><entry>100</entry><entry>101</entry><entry>98</entry><entry>97</entry><entry>74</entry><entry>73</entry><entry>65</entry></row><row><entry>12B6H4</entry><entry>100</entry><entry>101</entry><entry>100</entry><entry>93</entry><entry>41</entry><entry>66</entry><entry>54</entry></row></tbody></tgroup></table></tables><tables id="tabl0053" num="0053"><table frame="all"><title><u>Table 27:</u> KD values for wild type and humanised 12B6 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="48mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12B6</entry><entry>4.4</entry></row><row><entry>12B6H1</entry><entry>4.4</entry></row><row><entry>12B6H2</entry><entry>3.5</entry></row><row><entry>12B6H3</entry><entry>9</entry></row><row><entry>12B6H4</entry><entry>7.3</entry></row></tbody></tgroup></table></tables><tables id="tabl0054" num="0054"><table frame="all"><title><u>Table 28:</u> Sequence listing of humanised 12A2 nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="19mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="118mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12A2H1</entry><entry>90</entry><entry><img file="EP3415535A1_D0149.tif" /></entry></row><row><entry>12A2H3</entry><entry>91</entry><entry><img file="EP3415535A1_D0150.tif" /></entry></row><row><entry>12A2H4</entry><entry>92</entry><entry><img file="EP3415535A1_D0151.tif" /></entry></row><row><entry>12A2H11</entry><entry>93</entry><entry><img file="EP3415535A1_D0152.tif" /></entry></row><row><entry>12A2H13</entry><entry>94</entry><entry><img file="EP3415535A1_D0153.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0055" num="0055"><table frame="all"><title><u>Table 29:</u> Expression yields of wild type and humanised 12A2 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="52mm" /><colspec colnum="2" colname="col2" colwidth="72mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Yield (mg/l) after TALON or other purification</b></entry></row></thead><tbody><row><entry>12A2</entry><entry>18</entry></row><row><entry>12A2H1</entry><entry>11</entry></row><row><entry>12A2H3</entry><entry>11</entry></row><row><entry>12A2H4</entry><entry>11</entry></row><row><entry>12A2H11</entry><entry>15</entry></row><row><entry>12A2H13</entry><entry>11</entry></row></tbody></tgroup></table></tables><tables id="tabl0056" num="0056"><table frame="all"><title><u>Table 30</u>: Concentration of wild type and humanised 12A2 nanobodies after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="28mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><colspec colnum="3" colname="col3" colwidth="19mm" /><colspec colnum="4" colname="col4" colwidth="19mm" /><colspec colnum="5" colname="col5" colwidth="19mm" /><colspec colnum="6" colname="col6" colwidth="19mm" /><colspec colnum="7" colname="col7" colwidth="19mm" /><colspec colnum="8" colname="col8" colwidth="19mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>RT</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12A2</entry><entry>100</entry><entry>106</entry><entry>104</entry><entry>100</entry><entry>93</entry><entry>87</entry><entry>90</entry></row><row><entry>12A2H1</entry><entry>100</entry><entry>99</entry><entry>99</entry><entry>99</entry><entry>100</entry><entry>89</entry><entry>80</entry></row><row><entry>12A2H3</entry><entry>100</entry><entry>102</entry><entry>101</entry><entry>102</entry><entry>102</entry><entry>90</entry><entry>39</entry></row><row><entry>12A2H4</entry><entry>100</entry><entry>100</entry><entry>101</entry><entry>100</entry><entry>99</entry><entry>90</entry><entry>83</entry></row><row><entry>12A2H11</entry><entry>100</entry><entry>111</entry><entry>113</entry><entry>107</entry><entry>103</entry><entry>85</entry><entry>67</entry></row><row><entry>12A2H13</entry><entry>100</entry><entry>104</entry><entry>103</entry><entry>103</entry><entry>100</entry><entry>90</entry><entry>81</entry></row></tbody></tgroup></table></tables><tables id="tabl0057" num="0057"><table frame="all"><title><u>Table 31:</u> Platelet adhesion of wild type and humanised 12A2 nanobodies in perfusion chamber at 0.7 and 1.5 ug/ml</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="45mm" /><colspec colnum="2" colname="col2" colwidth="40mm" /><colspec colnum="3" colname="col3" colwidth="40mm" /><colspec colnum="4" colname="col4" colwidth="40mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col4" align="left" valign="top"><b>% Platelet adhesion</b></entry></row><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>0 µg/ml</b></entry><entry valign="top"><b>0.7 µg/ml</b></entry><entry valign="top"><b>1.5 µg/ml</b></entry></row></thead><tbody><row><entry>Control</entry><entry>73±4</entry><entry>-</entry><entry>-</entry></row><row><entry>12A2</entry><entry>-</entry><entry>36±3</entry><entry>34±5</entry></row><row><entry>12A2H1</entry><entry>-</entry><entry>49±1</entry><entry>47±3</entry></row><row><entry>12A2H3</entry><entry>-</entry><entry>62±4</entry><entry>63±1</entry></row><row><entry>12A2H4</entry><entry>-</entry><entry>55±1</entry><entry>54±1</entry></row><row><entry>12A2H11</entry><entry>-</entry><entry>57±1</entry><entry>52±1</entry></row><row><entry>12A2H13</entry><entry>-</entry><entry>67±4</entry><entry>67±4</entry></row></tbody></tgroup></table></tables><tables id="tabl0058" num="0058"><table frame="all"><title><u>Table 32:</u> Platelet adhesion of wild type and humanised 12A2 nanobodies in perfusion chamber at 0.5, 1 and 2 ug/ml</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="35mm" /><colspec colnum="2" colname="col2" colwidth="32mm" /><colspec colnum="3" colname="col3" colwidth="33mm" /><colspec colnum="4" colname="col4" colwidth="33mm" /><colspec colnum="5" colname="col5" colwidth="33mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col5" align="left" valign="top"><b>% Platelet adhesion</b></entry></row><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>0 µg/ml</b></entry><entry valign="top"><b>0.5 µg/ml</b></entry><entry valign="top"><b>1 µg/ml</b></entry><entry valign="top"><b>2 µg/ml</b></entry></row></thead><tbody><row><entry>Control</entry><entry>72±1</entry><entry>-</entry><entry>-</entry><entry>-</entry></row><row><entry>12A2</entry><entry>-</entry><entry>33±10</entry><entry>35±11</entry><entry>10±10</entry></row><row><entry>12A2H1</entry><entry>-</entry><entry>40±9</entry><entry>43±3</entry><entry>38±5</entry></row><row><entry>12A2H4</entry><entry>-</entry><entry>61±1</entry><entry>57±1</entry><entry>46±5</entry></row></tbody></tgroup></table></tables><tables id="tabl0059" num="0059"><table frame="all"><title><u>Table 33:</u> KD values for wild type and humanised 12A2 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="48mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12A2</entry><entry>3,1</entry></row><row><entry>12A2 H3</entry><entry>14,6</entry></row><row><entry>12A2 H11</entry><entry>10,6</entry></row><row><entry>12A2 H13</entry><entry>38,8</entry></row></tbody></tgroup></table></tables><tables id="tabl0060" num="0060"><table frame="all"><title><u>Table 34</u>: Sequence listing of humanised 12A5 nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="117mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12A5H1</entry><entry>95</entry><entry><img file="EP3415535A1_D0154.tif" /></entry></row><row><entry>12A5H2</entry><entry>96</entry><entry><img file="EP3415535A1_D0155.tif" /></entry></row><row><entry>12A5H3</entry><entry>97</entry><entry><img file="EP3415535A1_D0156.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0061" num="0061"><table frame="all"><title><u>Table 35:</u> Expression yields of wild type and humanised 12A5 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="52mm" /><colspec colnum="2" colname="col2" colwidth="52mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Yield (mg/l) after TALON</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>13</entry></row><row><entry>12A5H1</entry><entry>8</entry></row><row><entry>12A5H2</entry><entry>9</entry></row><row><entry>12A5H3</entry><entry>11</entry></row></tbody></tgroup></table></tables><tables id="tabl0062" num="0062"><table frame="all"><title><u>Table 36:</u> Concentration of wild type and humanised 12A5 nanobodies after heating at increasing temperatures</title><tgroup cols="7"><colspec colnum="1" colname="col1" colwidth="30mm" /><colspec colnum="2" colname="col2" colwidth="22mm" /><colspec colnum="3" colname="col3" colwidth="22mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="22mm" /><colspec colnum="6" colname="col6" colwidth="22mm" /><colspec colnum="7" colname="col7" colwidth="22mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>108</entry><entry>107</entry><entry>98</entry><entry>83</entry><entry>75</entry><entry>66</entry></row><row><entry>12A5H1</entry><entry>99</entry><entry>91</entry><entry>86</entry><entry>60</entry><entry>69</entry><entry>63</entry></row><row><entry>12A5H2</entry><entry>99</entry><entry>108</entry><entry>90</entry><entry>58</entry><entry>67</entry><entry>60</entry></row><row><entry>12A5H3</entry><entry>101</entry><entry>97</entry><entry>97</entry><entry>67</entry><entry>73</entry><entry>64</entry></row></tbody></tgroup></table></tables><tables id="tabl0063" num="0063"><table frame="all"><title><u>Table 37:</u> KD values for wild type and humanised 12A5 nanobodies</title><tgroup cols="2"><colspec colnum="1" colname="col1" colwidth="48mm" /><colspec colnum="2" colname="col2" colwidth="48mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>KD (nM)</b></entry></row></thead><tbody><row><entry>12A5</entry><entry>1,6</entry></row><row><entry>12A5H1</entry><entry>1,8</entry></row><row><entry>12A5H2</entry><entry>12,8</entry></row><row><entry>12A5H3</entry><entry>ND</entry></row></tbody></tgroup></table></tables><tables id="tabl0064" num="0064"><table frame="all"><title><u>Table 38:</u> Sequence listing of humanised bivalent nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="40mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="105mm" /><thead><row><entry valign="top"><b>Name</b></entry><entry valign="top"><b>SEQ ID NO</b></entry><entry valign="top"><b>Sequence</b></entry></row></thead><tbody><row><entry>12A2H1-3a-12A2H1</entry><entry>98</entry><entry><img file="EP3415535A1_D0157.tif" /></entry></row><row><entry>12A2H4-3a-12A2H4</entry><entry>99</entry><entry><img file="EP3415535A1_D0158.tif" /></entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>100</entry><entry><img file="EP3415535A1_D0159.tif" /></entry></row><row><entry>12A2H1-GS9-12A2H1</entry><entry>101</entry><entry><img file="EP3415535A1_D0160.tif" /></entry></row><row><entry>12A2H4-GS9-12A2H4</entry><entry>102</entry><entry><img file="EP3415535A1_D0161.tif" /></entry></row><row><entry>12B6H2-GS9-12B6H2</entry><entry>103</entry><entry><img file="EP3415535A1_D0162.tif" /></entry></row><row><entry>12A2H1-GS30-12A2H1</entry><entry>104</entry><entry><img file="EP3415535A1_D0163.tif" /></entry></row><row><entry>12A2H4-GS30-12A2H4</entry><entry>105</entry><entry><img file="EP3415535A1_D0164.tif" /></entry></row><row><entry>12B6H2-GS30-12B6H2</entry><entry>106</entry><entry><img file="EP3415535A1_D0165.tif" /></entry></row></tbody></tgroup></table></tables><tables id="tabl0065" num="0065"><table frame="all"><title><u>Table 39:</u> Expression yields of humanised bivalent nanobodies</title><tgroup cols="3"><colspec colnum="1" colname="col1" colwidth="36mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Tags</b></entry><entry valign="top"><b>Yield (mg/l)</b></entry></row></thead><tbody><row><entry>12A2H1-3a-12A2H1</entry><entry>Yes</entry><entry>5</entry></row><row><entry>12A2H1-3a-12A2H1</entry><entry>No</entry><entry>6</entry></row><row><entry>12A2H4-3a-12A2H4</entry><entry>Yes</entry><entry>10</entry></row><row><entry>12A2H4-3a-12A2H4</entry><entry>No</entry><entry>7</entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>Yes</entry><entry>10</entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>No</entry><entry>2</entry></row></tbody></tgroup></table></tables><tables id="tabl0066" num="0066"><table frame="all"><title><u>Table 40:</u> Concentration of humanised bivalent nanobody after heating at increasing temperatures</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="33mm" /><colspec colnum="2" colname="col2" colwidth="17mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="16mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="16mm" /><colspec colnum="7" colname="col7" colwidth="16mm" /><colspec colnum="8" colname="col8" colwidth="16mm" /><thead><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>Tags</b></entry><entry valign="top"><b>37°C</b></entry><entry valign="top"><b>50°C</b></entry><entry valign="top"><b>60°C</b></entry><entry valign="top"><b>70°C</b></entry><entry valign="top"><b>80°C</b></entry><entry valign="top"><b>90°C</b></entry></row></thead><tbody><row><entry>12A2H1-3a-12A2H1</entry><entry>Yes</entry><entry>98</entry><entry>96</entry><entry>93</entry><entry>63</entry><entry>8</entry><entry>9</entry></row><row><entry>12A2H1-3a-12A2H1</entry><entry>No</entry><entry>100</entry><entry>99</entry><entry>100</entry><entry>77</entry><entry>14</entry><entry>15</entry></row><row><entry>12A2H4-3a-12A2H4</entry><entry>Yes</entry><entry>100</entry><entry>99</entry><entry>95</entry><entry>9</entry><entry>6</entry><entry>9</entry></row><row><entry>12A2H4-3a-12H4</entry><entry>No</entry><entry>98</entry><entry>98</entry><entry>98</entry><entry>18</entry><entry>17</entry><entry>26</entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>Yes</entry><entry>100</entry><entry>91</entry><entry>85</entry><entry>7</entry><entry>6</entry><entry>7</entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>No</entry><entry>100</entry><entry>99</entry><entry>99</entry><entry>28</entry><entry>13</entry><entry>18</entry></row></tbody></tgroup></table></tables><tables id="tabl0067" num="0067"><table frame="all"><title><u>Table 41:</u> Platelet adhesion of wild type and humanised bivalent nanobodies</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="34mm" /><colspec colnum="2" colname="col2" colwidth="20mm" /><colspec colnum="3" colname="col3" colwidth="20mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="20mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col5" align="left" valign="top"><b>% Platelet adhesion</b></entry></row><row><entry valign="top"><b>Nanobody</b></entry><entry valign="top"><b>0 µg/ml</b></entry><entry valign="top"><b>0.15 µg/ml</b></entry><entry valign="top"><b>0.3 µg/ml</b></entry><entry valign="top"><b>0.6 µg/ml</b></entry></row></thead><tbody><row><entry>Control</entry><entry>65 ± 8</entry><entry>-</entry><entry>-</entry><entry>-</entry></row><row><entry>12B4-3a-12B6</entry><entry>-</entry><entry>50 ± 5</entry><entry>15 ± 6</entry><entry>8 ± 6</entry></row><row><entry>12B6H2-3a-12B6H2</entry><entry>-</entry><entry>53 ± 4</entry><entry>30 ± 16</entry><entry>17 ± 6</entry></row><row><entry>12A2-3a-12A2</entry><entry>-</entry><entry>36 ± 8</entry><entry>10 ± 8</entry><entry>4 ± 3</entry></row><row><entry>12A2H1-3a-12A2H1</entry><entry>-</entry><entry>54 ± 4</entry><entry>10 ± 11</entry><entry>12 ± 7</entry></row><row><entry>12A2H4-3a-12A2H4</entry><entry>-</entry><entry>38 ± 2</entry><entry>10 ± 6</entry><entry>8 ± 4</entry></row></tbody></tgroup></table></tables><tables id="tabl0068" num="0068"><table frame="all"><title><u>Table 42:</u> baboons used with the different test compounds in the Folts study</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="22mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="22mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="22mm" /><thead><row><entry valign="top"><b>Baboon</b> ID</entry><entry valign="top"><b>Sex</b></entry><entry valign="top"><b>Weight [kg]</b></entry><entry valign="top"><b>Left leg</b></entry><entry valign="top"><b>Right leg</b></entry></row></thead><tbody><row><entry><b>1</b></entry><entry>male</entry><entry>9,8</entry><entry /><entry>Control</entry></row><row><entry><b>2</b></entry><entry>male</entry><entry>10,0</entry><entry /><entry>Control</entry></row><row><entry><b>13</b></entry><entry>male</entry><entry>12,4</entry><entry /><entry>Reopro</entry></row><row><entry><b>14</b></entry><entry>male</entry><entry>9,5</entry><entry /><entry>Reopro</entry></row><row><entry><b>15</b></entry><entry>male</entry><entry>10,8</entry><entry /><entry>Reopro</entry></row><row><entry><b>16</b></entry><entry>male</entry><entry /><entry>ALX-0081</entry><entry /></row><row><entry><b>17</b></entry><entry>male</entry><entry>15,6</entry><entry /><entry>ALX-0081</entry></row><row><entry><b>18</b></entry><entry>mate</entry><entry>17,2</entry><entry /><entry>ALX-0081</entry></row><row><entry><b>20/22</b></entry><entry>male</entry><entry>12,7</entry><entry>ALX-0081</entry><entry>ALX-0081</entry></row><row><entry><b>21</b></entry><entry>female</entry><entry>8,0</entry><entry /><entry>ALX-0081</entry></row><row><entry><b>23</b></entry><entry>male</entry><entry /><entry /><entry>ALX-0081</entry></row><row><entry><b>24</b></entry><entry>male</entry><entry>9,4</entry><entry>ALX-0081</entry><entry /></row><row><entry><b>3/19</b></entry><entry>male</entry><entry>15,2</entry><entry>Aspegic</entry><entry>ALX-0081</entry></row><row><entry><b>4</b></entry><entry>female</entry><entry>13,6</entry><entry>Aspegic</entry><entry /></row><row><entry><b>5</b></entry><entry>male</entry><entry>17,4</entry><entry>Aspegic</entry><entry /></row><row><entry><b>9</b></entry><entry>male</entry><entry>13,2</entry><entry>Plavix</entry><entry /></row><row><entry><b>6/10</b></entry><entry>male</entry><entry>10,2</entry><entry>Heparin</entry><entry>Plavix</entry></row><row><entry><b>7/11</b></entry><entry>male</entry><entry>9.4</entry><entry>Heparin</entry><entry>Plavix</entry></row><row><entry><b>8/12</b></entry><entry>male</entry><entry>10,5</entry><entry>Heparin</entry><entry>Plavix</entry></row></tbody></tgroup></table></tables><tables id="tabl0069" num="0069"><table frame="all"><title><u>Table 43:</u> Length of CFRs (s) for control animals (ND= not done)</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="24mm" /><colspec colnum="2" colname="col2" colwidth="24mm" /><colspec colnum="3" colname="col3" colwidth="22mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><thead><row><entry valign="top"><b>Control</b></entry><entry valign="top" /><entry namest="col3" nameend="col4" align="left" valign="top"><b>Baboon ID</b></entry></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>1</b></entry><entry valign="top"><b>2</b></entry></row></thead><tbody><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>291</entry><entry>249</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>294</entry><entry>278</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>427</entry><entry>185</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>285</entry><entry>203</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>438</entry><entry>175</entry></row></tbody></tgroup></table></tables><tables id="tabl0070" num="0070"><table frame="all"><title><u>Table 44:</u> Length of CFRs (s) for animals treated with Aspegic™ (ND= not done)</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="26mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><colspec colnum="3" colname="col3" colwidth="20mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="20mm" /><thead><row><entry valign="top"><b>Aspegic</b></entry><entry valign="top" /><entry namest="col3" nameend="col5" align="left" valign="top"><b>Baboon tD</b></entry></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>3</b></entry><entry valign="top"><b>4</b></entry><entry valign="top"><b>5</b></entry></row></thead><tbody><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>88</entry><entry>no CFRs</entry><entry>148</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>147</entry><entry>204</entry><entry>184</entry></row><row><entry><b>1 mg/kg</b></entry><entry><b>1 mg/kg</b></entry><entry>149</entry><entry>164</entry><entry>135</entry></row><row><entry><b>2,5 mg/kg</b></entry><entry><b>1,5 mg/kg</b></entry><entry>102</entry><entry>325</entry><entry>115</entry></row><row><entry><b>5 mg/kg</b></entry><entry><b>2,5 mg/kg</b></entry><entry>102</entry><entry>1800</entry><entry>245</entry></row><row><entry><b>10 mg/kg</b></entry><entry><b>5 mg/kg</b></entry><entry>113</entry><entry>905</entry><entry>156</entry></row><row><entry><b>20 mg/kg</b></entry><entry><b>10 mg/kg</b></entry><entry>125</entry><entry>657</entry><entry>169</entry></row><row><entry><b>40 mg/kg</b></entry><entry><b>20mg/kg</b></entry><entry>110</entry><entry>ND</entry><entry>145</entry></row><row><entry><b>80 mg/kg</b></entry><entry><b>40mg/kg</b></entry><entry>129</entry><entry>ND</entry><entry>ND</entry></row><row><entry namest="col1" nameend="col2" align="left"><b>Epinephrin</b></entry><entry>ND</entry><entry>161</entry><entry>ND</entry></row></tbody></tgroup></table></tables><tables id="tabl0071" num="0071"><table frame="all"><title><u>Table 45:</u> Length of CFRs (s) for animals treated with Heparin™ (ND= not done)</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="25mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><colspec colnum="3" colname="col3" colwidth="23mm" /><colspec colnum="4" colname="col4" colwidth="21mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><thead><row><entry valign="top"><b>Heparin</b></entry><entry valign="top" /><entry namest="col3" nameend="col5" align="left" valign="top"><b>Baboon ID</b></entry></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>6</b></entry><entry valign="top"><b>7</b></entry><entry valign="top"><b>8</b></entry></row></thead><tbody><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>232</entry><entry>113</entry><entry>166</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>298</entry><entry>131</entry><entry>246</entry></row><row><entry><b>15 IU/kg</b></entry><entry><b>15 IU/kg</b></entry><entry>630</entry><entry>208</entry><entry>255</entry></row><row><entry><b>30 IU/kg</b></entry><entry><b>30 IU/kg</b></entry><entry>355</entry><entry>241</entry><entry>320</entry></row><row><entry><b>60 IU/kg</b></entry><entry><b>60 IU/kg</b></entry><entry>432</entry><entry>246</entry><entry>332</entry></row><row><entry><b>120 IU/kg</b></entry><entry><b>120 IU/kg</b></entry><entry>610</entry><entry>160</entry><entry>206</entry></row><row><entry><b>240 IU/kg</b></entry><entry><b>240 IU/kg</b></entry><entry>>1800</entry><entry>221</entry><entry>169</entry></row><row><entry namest="col1" nameend="col2" align="left"><b>Epinephrin</b></entry><entry>109</entry><entry>65</entry><entry>ND</entry></row></tbody></tgroup></table></tables><tables id="tabl0072" num="0072"><table frame="all"><title><u>Table 46:</u> Length of CFRs (s) for animals treated with Plavix™ (ND= not done)</title><tgroup cols="6"><colspec colnum="1" colname="col1" colwidth="20mm" /><colspec colnum="2" colname="col2" colwidth="20mm" /><colspec colnum="3" colname="col3" colwidth="18mm" /><colspec colnum="4" colname="col4" colwidth="18mm" /><colspec colnum="5" colname="col5" colwidth="18mm" /><colspec colnum="6" colname="col6" colwidth="18mm" /><thead><row><entry valign="top">Plavix</entry><entry valign="top" /><entry namest="col3" nameend="col6" align="left" valign="top"><b>Baboon ID</b></entry></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>9</b></entry><entry valign="top"><b>10</b></entry><entry valign="top"><b>11</b></entry><entry valign="top"><b>12</b></entry></row></thead><tbody><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>215</entry><entry>178</entry><entry>84</entry><entry>144</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>168</entry><entry>160</entry><entry>88</entry><entry>189</entry></row><row><entry><b>1 mg/kg</b></entry><entry><b>1 mg/kg</b></entry><entry>189</entry><entry>ND</entry><entry>132</entry><entry>179</entry></row><row><entry><b>2,5 mg/kg</b></entry><entry><b>2,5 mg/kg</b></entry><entry>883</entry><entry>400</entry><entry>258</entry><entry>>1800</entry></row><row><entry><b>5 mg/kg</b></entry><entry><b>2,5 mg/kg</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>10 mg/kg</b></entry><entry><b>5 mg/kg</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>20 mg/kg</b></entry><entry><b>10 mg/kg</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry namest="col1" nameend="col2" align="left"><b>Epinephrin</b></entry><entry>241</entry><entry>91</entry><entry>83</entry><entry>66</entry></row></tbody></tgroup></table></tables><tables id="tabl0073" num="0073"><table frame="all"><title><u>Table 47:</u> Length of CFRs (s) for animals treated with Reopro™ (ND= not done)</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="26mm" /><colspec colnum="2" colname="col2" colwidth="26mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="21mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><thead><row><entry valign="top"><b>Reopro</b></entry><entry valign="top" /><entry namest="col3" nameend="col5" align="left" valign="top"><b>Baboon</b> ID</entry></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>13</b></entry><entry valign="top"><b>14</b></entry><entry valign="top"><b>15</b></entry></row></thead><tbody><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>144</entry><entry>90</entry><entry>308</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>141</entry><entry>103</entry><entry>268</entry></row><row><entry><b>20µg/kg</b></entry><entry><b>20 µg/kg</b></entry><entry>98</entry><entry>82</entry><entry>254</entry></row><row><entry><b>70 µg/kg</b></entry><entry><b>50 µg/kg</b></entry><entry>90</entry><entry>90</entry><entry>248</entry></row><row><entry><b>170µg/kg</b></entry><entry><b>100µg/kg</b></entry><entry>90</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>420µg/kg</b></entry><entry><b>2S0µg/kg</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>920 µg/kg</b></entry><entry><b>500 g/kg</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry namest="col1" nameend="col2" align="left"><b>Epinephrin</b></entry><entry>>1200</entry><entry>>1200</entry><entry>>1200</entry></row></tbody></tgroup></table></tables><tables id="tabl0074" num="0074"><table frame="all"><title><u>Table 48:</u> Length of CFRs (s) for animals treated with ALX-0081 (ND= not done)</title><tgroup cols="11"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="31mm" /><colspec colnum="3" colname="col3" colwidth="13mm" /><colspec colnum="4" colname="col4" colwidth="13mm" /><colspec colnum="5" colname="col5" colwidth="13mm" /><colspec colnum="6" colname="col6" colwidth="13mm" /><colspec colnum="7" colname="col7" colwidth="13mm" /><colspec colnum="8" colname="col8" colwidth="13mm" /><colspec colnum="9" colname="col9" colwidth="13mm" /><colspec colnum="10" colname="col10" colwidth="13mm" /><colspec colnum="11" colname="col11" colwidth="13mm" /><thead><row><entry valign="top"><b>ALX-0081</b></entry><entry valign="top" /><entry namest="col3" nameend="col11" align="left" valign="top"><b>Baboon ID</b></entry></row></thead><tbody><row><entry><b>Final dose</b></entry><entry><b>Dose</b></entry><entry><b>16</b></entry><entry><b>17</b></entry><entry><b>18</b></entry><entry><b>19</b></entry><entry><b>20</b></entry><entry><b>21</b></entry><entry><b>22</b></entry><entry><b>23</b></entry><entry><b>24</b></entry></row><row><entry><b>0</b></entry><entry><b>control</b></entry><entry>168</entry><entry>293</entry><entry>185</entry><entry>90</entry><entry>94</entry><entry>117</entry><entry>188</entry><entry>164</entry><entry>161</entry></row><row><entry><b>0</b></entry><entry><b>saline</b></entry><entry>151</entry><entry>236</entry><entry>242</entry><entry>117</entry><entry>98</entry><entry>107</entry><entry>233</entry><entry>105</entry><entry>178</entry></row><row><entry><b>3 µg/kg</b></entry><entry><b>3 microgram/kg</b></entry><entry>193</entry><entry>ND</entry><entry>ND</entry><entry>144</entry><entry>133</entry><entry>183</entry><entry>312</entry><entry>112</entry><entry>295</entry></row><row><entry><b>13 µg/kg</b></entry><entry><b>10 microgram/kg</b></entry><entry>913</entry><entry valign="bottom">>1800</entry><entry>298</entry><entry>237</entry><entry>620</entry><entry>525</entry><entry valign="bottom">>1800</entry><entry>213</entry><entry>380</entry></row><row><entry><b>43 µg/kg</b></entry><entry><b>30 microgram/kg</b></entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry></row><row><entry><b>133 µg/kg</b></entry><entry><b>90 microgram/kg</b></entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry></row><row><entry><b>403 µg/kg</b></entry><entry><b>270 microgram/kg</b></entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry><entry valign="bottom">>1800</entry></row><row><entry><b>Epinephrin</b></entry><entry /><entry valign="bottom">>1200</entry><entry valign="bottom">>1200</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry><entry valign="bottom">>900</entry></row></tbody></tgroup></table></tables><tables id="tabl0075" num="0075"><table frame="all"><title><u>Table 49:</u> baboons used with the different test compounds in the Folts study</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="27mm" /><colspec colnum="2" colname="col2" colwidth="26mm" /><colspec colnum="3" colname="col3" colwidth="26mm" /><colspec colnum="4" colname="col4" colwidth="32mm" /><thead><row><entry valign="top"><b>Baboon ID</b></entry><entry valign="top"><b>Sex</b></entry><entry valign="top"><b>Weight [kg]</b></entry><entry valign="top"><b>Mix</b></entry></row></thead><tbody><row><entry><b>1</b></entry><entry>Male</entry><entry>9,8</entry><entry>Asp/Hep/Plav/ALX</entry></row><row><entry><b>2</b></entry><entry>Female</entry><entry>13,6</entry><entry>Asp/Hep/Plav/ALX</entry></row><row><entry><b>3</b></entry><entry>Female</entry><entry>7,8</entry><entry>Asp/Hep/Ptav/ALX</entry></row><row><entry><b>4</b></entry><entry>Male</entry><entry>12,1</entry><entry>Asp/Hep/Plav/ALX</entry></row><row><entry><b>5</b></entry><entry>Male</entry><entry>11,4</entry><entry>Asp/Hep/Plav/ALX</entry></row><row><entry><b>6</b></entry><entry>Male</entry><entry>11,4</entry><entry>Asp/Hep/Plav/ALX</entry></row><row><entry><b>7</b></entry><entry>Male</entry><entry>14,0</entry><entry>Asp/Hep/Plav/ALX</entry></row></tbody></tgroup></table></tables><tables id="tabl0076" num="0076"><table frame="all"><title><u>Table 50</u>: Inhibition of CFRs in the Folts model for the different drugs tested. The number of experiments in which an inhibition of CFRs was observed in the mentioned different conditions is shown as a function of the total number of independent repeats of that condition.</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="29mm" /><colspec colnum="2" colname="col2" colwidth="33mm" /><colspec colnum="3" colname="col3" colwidth="33mm" /><colspec colnum="4" colname="col4" colwidth="44mm" /><colspec colnum="5" colname="col5" colwidth="29mm" /><thead><row><entry valign="top"><b>Test compound</b></entry><entry valign="top"><b>Inhibition of CFRs</b></entry><entry valign="top"><b>Inhibition of CFRs after new injury</b></entry><entry valign="top"><b>Inhibition of CFRs after administration of Epinephrin</b></entry><entry valign="top"><b>Effective dose</b></entry></row></thead><tbody><row><entry><b>Control</b></entry><entry>0/2</entry><entry>ND</entry><entry>ND</entry><entry>-</entry></row><row><entry><b>Aspegic</b></entry><entry>0/3</entry><entry>0/3</entry><entry>0/1</entry><entry>-</entry></row><row><entry><b>Heparin</b></entry><entry>1/3</entry><entry>1/3</entry><entry>0/2</entry><entry>-</entry></row><row><entry><b>Plavix</b></entry><entry>4/4</entry><entry>4/4</entry><entry>0/4</entry><entry>5 mg/kg</entry></row><row><entry><b>Reopro</b></entry><entry>3/3</entry><entry>3/3</entry><entry>3/3</entry><entry>170-420 µg/kg</entry></row><row><entry><b>ALX-0081</b></entry><entry>9/9</entry><entry>9/9</entry><entry>9/9</entry><entry>13-43 µg/kg + 1,5 x dose/kg/hour</entry></row></tbody></tgroup></table></tables><tables id="tabl0077" num="0077"><table frame="all"><title><u>Table 51:</u> Length of CFRs (seconds) for each baboon and each dose of Aspegic, Heparin, Plavix and ALX-0081. The effective dose is indicated in yellow</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="41mm" /><colspec colnum="2" colname="col2" colwidth="18mm" /><colspec colnum="3" colname="col3" colwidth="18mm" /><colspec colnum="4" colname="col4" colwidth="18mm" /><colspec colnum="5" colname="col5" colwidth="18mm" /><colspec colnum="6" colname="col6" colwidth="18mm" /><colspec colnum="7" colname="col7" colwidth="18mm" /><colspec colnum="8" colname="col8" colwidth="18mm" /><thead><row><entry valign="top" /><entry valign="top"><b>4</b></entry><entry valign="top"><b>5</b></entry><entry valign="top"><b>6</b></entry><entry valign="top"><b>7</b></entry><entry valign="top"><b>8</b></entry><entry valign="top"><b>9</b></entry><entry valign="top"><b>10</b></entry></row></thead><tbody><row><entry><b>control</b></entry><entry>82</entry><entry>99</entry><entry>109</entry><entry>95</entry><entry>113</entry><entry>142</entry><entry>113</entry></row><row><entry><b>saline</b></entry><entry>113</entry><entry>119</entry><entry>108</entry><entry>114</entry><entry>131</entry><entry>168</entry><entry>92</entry></row><row><entry><b>5 mg/kg Aspegic + 60 IU/kg Heparin + 1 mg/kg Plavix</b></entry><entry>153</entry><entry>135</entry><entry>272</entry><entry>742</entry><entry>146</entry><entry>219</entry><entry>223</entry></row><row><entry><b>+1 mg/kg Plavix</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>Epinephrin + non effective doses ALX-0081 + Heparin</b></entry><entry>250</entry><entry>72</entry><entry>87</entry><entry>95</entry><entry>106</entry><entry>105</entry><entry>105</entry></row><row><entry><b>Epinephrin + effective dose ALX-0081</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row></tbody></tgroup></table></tables><tables id="tabl0078" num="0078"><table frame="all"><title><u>Table 52:</u> Blood loss relative to the second control gauze for animals treated with Plavix™ in function of final dose (STD= standard deviation</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="23mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><colspec colnum="3" colname="col3" colwidth="20mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="20mm" /><colspec colnum="6" colname="col6" colwidth="21mm" /><colspec colnum="7" colname="col7" colwidth="24mm" /><colspec colnum="8" colname="col8" colwidth="19mm" /><thead><row><entry valign="top"><b>Plavix</b></entry><entry valign="top" /><entry namest="col3" nameend="col6" align="left" valign="top"><b>Baboon ID</b></entry><entry valign="top" /><entry valign="top" /></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>9</b></entry><entry valign="top"><b>10</b></entry><entry valign="top"><b>11</b></entry><entry valign="top"><b>12</b></entry><entry valign="top"><b>Average</b></entry><entry valign="top"><b>STD</b></entry></row></thead><tbody><row><entry><b>1 mg/kg</b></entry><entry><b>1 mg/kg</b></entry><entry>0,6</entry><entry>1,3</entry><entry>1,6</entry><entry>1,2</entry><entry><b>1,4</b></entry><entry><b>0,2</b></entry></row><row><entry><b>2,5 mg/kg</b></entry><entry><b>1,5 mg/kg</b></entry><entry>1,5</entry><entry>1,4</entry><entry>1,1</entry><entry>1,0</entry><entry><b>1,2</b></entry><entry><b>0,2</b></entry></row><row><entry><b>5 mg/kg</b></entry><entry><b>2,5 mg/kg</b></entry><entry>5,1</entry><entry>4,7</entry><entry>1,4</entry><entry>6,6</entry><entry><b>4,5</b></entry><entry><b>2,2</b></entry></row><row><entry><b>10 mg/kg</b></entry><entry><b>5 mg/kg</b></entry><entry>6,5</entry><entry>4,5</entry><entry>5,8</entry><entry>13,6</entry><entry><b>7,6</b></entry><entry><b>4,1</b></entry></row><row><entry><b>20 mg/kg</b></entry><entry><b>10 mg/kg</b></entry><entry>3,7</entry><entry>4,1</entry><entry>9,1</entry><entry>2,6</entry><entry><b>4,9</b></entry><entry><b>2,9</b></entry></row></tbody></tgroup></table></tables><tables id="tabl0079" num="0079"><table frame="all"><title><u>Table 53:</u> Blood loss relative to the second control gauze for animals treated with Rcopro™ in function of final dose (STD= standard deviation)</title><tgroup cols="7"><colspec colnum="1" colname="col1" colwidth="27mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><colspec colnum="3" colname="col3" colwidth="22mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="22mm" /><colspec colnum="6" colname="col6" colwidth="25mm" /><colspec colnum="7" colname="col7" colwidth="23mm" /><thead><row><entry valign="top"><b>Reopro</b></entry><entry valign="top" /><entry namest="col3" nameend="col5" align="left" valign="top"><b>Baboon ID</b></entry><entry valign="top" /><entry valign="top" /></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>13</b></entry><entry valign="top"><b>14</b></entry><entry valign="top"><b>15</b></entry><entry valign="top"><b>Average</b></entry><entry valign="top"><b>STD</b></entry></row></thead><tbody><row><entry><b>2Oµg/kg</b></entry><entry><b>20 µg/kg</b></entry><entry>2,7</entry><entry>0,6</entry><entry>2,1</entry><entry><b>1,8</b></entry><entry><b>1</b></entry></row><row><entry><b>70µg/kg</b></entry><entry><b>50 µg/kg</b></entry><entry>1,2</entry><entry>2,1</entry><entry>0,4</entry><entry><b>1,2</b></entry><entry><b>1</b></entry></row><row><entry><b>170µg/kg</b></entry><entry><b>100 µg/kg</b></entry><entry>1,2</entry><entry>6,0</entry><entry>4,7</entry><entry><b>4,0</b></entry><entry><b>2</b></entry></row><row><entry><b>420µg/kg</b></entry><entry><b>250µg/kg</b></entry><entry>28,3</entry><entry>7,1</entry><entry>13,9</entry><entry><b>16,4</b></entry><entry><b>11</b></entry></row><row><entry><b>920µg/kg</b></entry><entry><b>500µg/kg</b></entry><entry>39,8</entry><entry>14,5</entry><entry>6,3</entry><entry><b>20,2</b></entry><entry><b>17</b></entry></row></tbody></tgroup></table></tables><tables id="tabl0080" num="0080"><table frame="all"><title><u>Table 54:</u> Blood loss relative to the second control gauze for animals treated with ALX-0081in function of final dose (STD= standard deviation)</title><tgroup cols="12"><colspec colnum="1" colname="col1" colwidth="18mm" /><colspec colnum="2" colname="col2" colwidth="14mm" /><colspec colnum="3" colname="col3" colwidth="13mm" /><colspec colnum="4" colname="col4" colwidth="13mm" /><colspec colnum="5" colname="col5" colwidth="13mm" /><colspec colnum="6" colname="col6" colwidth="13mm" /><colspec colnum="7" colname="col7" colwidth="13mm" /><colspec colnum="8" colname="col8" colwidth="13mm" /><colspec colnum="9" colname="col9" colwidth="14mm" /><colspec colnum="10" colname="col10" colwidth="13mm" /><colspec colnum="11" colname="col11" colwidth="18mm" /><colspec colnum="12" colname="col12" colwidth="15mm" /><thead><row><entry valign="top"><b>ALX-0081</b></entry><entry valign="top" /><entry namest="col3" nameend="col10" align="left" valign="top"><b>Baboon ID</b></entry><entry valign="top" /><entry valign="top" /></row><row><entry valign="top"><b>Final dose</b></entry><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>17</b></entry><entry valign="top"><b>18</b></entry><entry valign="top"><b>19</b></entry><entry valign="top"><b>20</b></entry><entry valign="top"><b>21</b></entry><entry valign="top"><b>22</b></entry><entry valign="top"><b>23</b></entry><entry valign="top"><b>24</b></entry><entry valign="top"><b>Average</b></entry><entry valign="top"><b>STD</b></entry></row></thead><tbody><row><entry><b>3 µg/kg</b></entry><entry><b>3 µg/kg</b></entry><entry>ND</entry><entry>ND</entry><entry>0,4</entry><entry>1,2</entry><entry>0,5</entry><entry>1,1</entry><entry>1,8</entry><entry>0,8</entry><entry>1,0</entry><entry>0,5</entry></row><row><entry><b>13 µg/kg</b></entry><entry><b>10 µg/kg</b></entry><entry>1,2</entry><entry>0.8</entry><entry>0,1</entry><entry>1,2</entry><entry>1,1</entry><entry>1,3</entry><entry>1,1</entry><entry>1,1</entry><entry>1,0</entry><entry>0,4</entry></row><row><entry><b>43 µg/kg</b></entry><entry><b>30 µg/kg</b></entry><entry>2,8</entry><entry>2,0</entry><entry>4,1</entry><entry>3,9</entry><entry>2,1</entry><entry>3,8</entry><entry>3,0</entry><entry>1,6</entry><entry>2,9</entry><entry>1,0</entry></row><row><entry><b>133 µg/kg</b></entry><entry><b>90 µg/kg</b></entry><entry>2,5</entry><entry>3,1</entry><entry>2,0</entry><entry>0.4</entry><entry>4,0</entry><entry>5,3</entry><entry>5,6</entry><entry>1,4</entry><entry>3,0</entry><entry>1,8</entry></row><row><entry><b>403 µg/kg</b></entry><entry><b>270 µg/kg</b></entry><entry>2,6</entry><entry>2,3</entry><entry>2,3</entry><entry>0,4</entry><entry>0.8</entry><entry>5.6</entry><entry>10,7</entry><entry>0,9</entry><entry>3,2</entry><entry>3,4</entry></row></tbody></tgroup></table></tables><tables id="tabl0081" num="0081"><table frame="all"><title><u>Table 55:</u> The average of the total amount of blood loss (= sum of blood loss from the first five doses of test compound) as relative to the second control gauze</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="42mm" /><colspec colnum="2" colname="col2" colwidth="40mm" /><colspec colnum="3" colname="col3" colwidth="39mm" /><colspec colnum="4" colname="col4" colwidth="45mm" /><thead><row><entry valign="middle"><b>Test compound</b></entry><entry valign="middle"><b>Total dose as multiple of effective dose</b></entry><entry valign="middle"><b>Average of total blood loss</b></entry><entry valign="middle"><b>Standard deviation of blood loss</b></entry></row></thead><tbody><row><entry valign="middle"><b>Plavlx</b></entry><entry valign="middle">4</entry><entry valign="middle">19,4</entry><entry valign="middle">4,0</entry></row><row><entry valign="middle"><b>Reopro</b></entry><entry valign="middle">3,5</entry><entry valign="middle">44</entry><entry valign="middle">26</entry></row><row><entry valign="middle"><b>ALX-0081</b></entry><entry valign="middle">13</entry><entry valign="middle">10,8</entry><entry valign="middle">5,7</entry></row></tbody></tgroup></table></tables><tables id="tabl0082" num="0082"><table frame="all"><title><u>Table 56:</u> Blood loss in gauzes relative to the second control gauze for each baboon treated with Aspegic, Heparin, Plavix and ALX-0081 in function of drug dose. The effective drug dose in which a complete inhibition of CFRs was observed, is indicated in yellow</title><tgroup cols="9"><colspec colnum="1" colname="col1" colwidth="45mm" /><colspec colnum="2" colname="col2" colwidth="16mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="14mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="14mm" /><colspec colnum="7" colname="col7" colwidth="14mm" /><colspec colnum="8" colname="col8" colwidth="14mm" /><colspec colnum="9" colname="col9" colwidth="20mm" /><thead><row><entry valign="top" /><entry valign="top"><b>4</b></entry><entry valign="top"><b>5</b></entry><entry valign="top"><b>6</b></entry><entry valign="top"><b>7</b></entry><entry valign="top"><b>8</b></entry><entry valign="top"><b>9</b></entry><entry valign="top"><b>10</b></entry><entry valign="top"><b>median± STD</b></entry></row></thead><tbody><row><entry><b>5 mg/kg Aspegic + 60 IU/kg Heparin + 1 mg/kg Plavix</b></entry><entry>2,6</entry><entry>1</entry><entry>4,6</entry><entry>12,1</entry><entry>1,3</entry><entry>1,4</entry><entry>1,8</entry><entry>1,8 ± 3,5</entry></row><row><entry><b>+ 1 mg/kg Plavix</b></entry><entry>3,7</entry><entry>13,9</entry><entry>4,8</entry><entry>13,1</entry><entry>1,4</entry><entry>4,3</entry><entry>5,6</entry><entry>4,8 ± 6,7</entry></row><row><entry><b>Epinephrin + non effective doses ALX-0081 + Heparin</b></entry><entry>9,4</entry><entry>2,7</entry><entry>2,7</entry><entry>67</entry><entry>0,3</entry><entry>4,8</entry><entry>9,2</entry><entry>4,8 ± 13,7</entry></row><row><entry><b>Epinephrin + effective dose ALX-0081</b></entry><entry>23,4</entry><entry>2,0</entry><entry>1</entry><entry>39,4</entry><entry>1,3</entry><entry>4,5</entry><entry>0,8</entry><entry>2,0 ± 10,3</entry></row></tbody></tgroup></table></tables><tables id="tabl0083" num="0083"><table frame="all"><title><u>Table 57:</u> % ristocetin-induced platelet aggregation for each baboon treated with Aspegic, Heparin, Plavix and ALX-0081 in function of drug dose</title><tgroup cols="8"><colspec colnum="1" colname="col1" colwidth="57mm" /><colspec colnum="2" colname="col2" colwidth="16mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="16mm" /><colspec colnum="5" colname="col5" colwidth="16mm" /><colspec colnum="6" colname="col6" colwidth="16mm" /><colspec colnum="7" colname="col7" colwidth="16mm" /><colspec colnum="8" colname="col8" colwidth="16mm" /><thead><row><entry valign="top" /><entry valign="top"><b>4</b></entry><entry valign="top"><b>5</b></entry><entry valign="top"><b>6</b></entry><entry valign="top"><b>7</b></entry><entry valign="top"><b>8</b></entry><entry valign="top"><b>9</b></entry><entry valign="top"><b>10</b></entry></row></thead><tbody><row><entry><b>control</b></entry><entry>75</entry><entry>78</entry><entry>79</entry><entry>70</entry><entry>46</entry><entry>70</entry><entry>46</entry></row><row><entry><b>saline</b></entry><entry>48</entry><entry>78</entry><entry>74</entry><entry>24</entry><entry>45</entry><entry>65</entry><entry>47</entry></row><row><entry><b>5 mg/kg Aspegic + 60 IU/kg Heparin + 1 mg/kg Plavix</b></entry><entry>62</entry><entry>65</entry><entry>89</entry><entry>64</entry><entry>66</entry><entry>68</entry><entry>55</entry></row><row><entry><b>+ 1 mg/kg Plavix</b></entry><entry>42</entry><entry>63</entry><entry>66</entry><entry>83</entry><entry>59</entry><entry>76</entry><entry>60</entry></row><row><entry><b>Epinephrin + effective dose ALX-0081</b></entry><entry>0</entry><entry>24</entry><entry>24</entry><entry>6</entry><entry>17</entry><entry>7</entry><entry>8</entry></row></tbody></tgroup></table></tables><tables id="tabl0084" num="0084"><table frame="all"><title><u>Table 58</u>: concentration of ALX-0081 [µg/ml] in blood samples obtained at 10 minutes after administration</title><tgroup cols="11"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="21mm" /><colspec colnum="3" colname="col3" colwidth="13mm" /><colspec colnum="4" colname="col4" colwidth="13mm" /><colspec colnum="5" colname="col5" colwidth="13mm" /><colspec colnum="6" colname="col6" colwidth="15mm" /><colspec colnum="7" colname="col7" colwidth="13mm" /><colspec colnum="8" colname="col8" colwidth="13mm" /><colspec colnum="9" colname="col9" colwidth="13mm" /><colspec colnum="10" colname="col10" colwidth="15mm" /><colspec colnum="11" colname="col11" colwidth="15mm" /><thead><row><entry valign="top"><b>ALX-0081</b></entry><entry valign="top" /><entry namest="col3" nameend="col11" align="left" valign="top"><b>Baboon ID</b></entry></row></thead><tbody><row><entry><b>Final dose</b></entry><entry><b>Dose</b></entry><entry><b>16</b></entry><entry><b>17</b></entry><entry><b>18</b></entry><entry><b>19</b></entry><entry><b>20</b></entry><entry><b>21</b></entry><entry><b>22</b></entry><entry><b>23</b></entry><entry><b>24</b></entry></row><row><entry><b>3 µg/kg</b></entry><entry><b>3 µg/kg</b></entry><entry>0,10</entry><entry /><entry /><entry>0,03</entry><entry>0,05</entry><entry>0,08</entry><entry>0,04</entry><entry>0,14</entry><entry>0,08</entry></row><row><entry><b>13 µg/kg</b></entry><entry><b>10 µg/kg</b></entry><entry>1,23</entry><entry>0,34</entry><entry>0,29</entry><entry>0,26</entry><entry>0,50</entry><entry>0,39</entry><entry>0,41</entry><entry>0,18</entry><entry>0,42</entry></row><row><entry><b>43 µg/kg</b></entry><entry><b>30 µg/kg</b></entry><entry>1,00</entry><entry>0,51</entry><entry>0,72</entry><entry>1,14</entry><entry>1,01</entry><entry>0,61</entry><entry>1,01</entry><entry>0,87</entry><entry>1,21</entry></row><row><entry><b>133 µg/kg</b></entry><entry><b>90 µg/kg</b></entry><entry>1,87</entry><entry>1,38</entry><entry>1,77</entry><entry>1,61</entry><entry>2,64</entry><entry>1,60</entry><entry>6,77</entry><entry>2,75</entry><entry>5,01</entry></row><row><entry><b>403 µg/kg</b></entry><entry><b>270 µg/kg</b></entry><entry>6,77</entry><entry>4,03</entry><entry>6,73</entry><entry>35,14</entry><entry>7,66</entry><entry>6,01</entry><entry>9,24</entry><entry>18,56</entry><entry>16,62</entry></row></tbody></tgroup></table></tables><tables id="tabl0085" num="0085"><table frame="all"><title><u>Table 59:</u> Length of CFRs seconds for baboons treated with ALX-0081 and with vWF</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="57mm" /><colspec colnum="2" colname="col2" colwidth="30mm" /><colspec colnum="3" colname="col3" colwidth="30mm" /><colspec colnum="4" colname="col4" colwidth="30mm" /><thead><row><entry valign="top" /><entry namest="col2" nameend="col4" align="left" valign="top"><b>Baboon ID</b></entry></row><row><entry valign="top"><b>Dose</b></entry><entry valign="top"><b>1</b></entry><entry valign="top"><b>2</b></entry><entry valign="top"><b>3</b></entry></row></thead><tbody><row><entry><b>Control</b></entry><entry>119</entry><entry>140</entry><entry>111</entry></row><row><entry><b>Saline</b></entry><entry>ND</entry><entry>158</entry><entry>158</entry></row><row><entry><b>30 µg/kg + 45 µg/kg/hour ALX-0081</b></entry><entry>>1800</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>250 IU vWF</b></entry><entry>>420</entry><entry>>1800</entry><entry>>1800</entry></row><row><entry><b>250 IU vWF</b></entry><entry>246</entry><entry>256</entry><entry>230</entry></row></tbody></tgroup></table></tables><tables id="tabl0086" num="0086"><table frame="all"><title><u>Table 60:</u> Volumes [µl] to prepare the different mixtures for study of cleavage of A1A2A3 by ADAMTS13</title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="36mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><colspec colnum="3" colname="col3" colwidth="29mm" /><colspec colnum="4" colname="col4" colwidth="30mm" /><colspec colnum="5" colname="col5" colwidth="27mm" /><thead><row><entry valign="top" /><entry valign="top"><b>NPP</b></entry><entry valign="top"><b>NPP + EDTA</b></entry><entry valign="top"><b>NPP + ALX-0081</b></entry><entry valign="top"><b>PBS</b></entry></row></thead><tbody><row><entry>Tris (100 mM)</entry><entry>5</entry><entry>5</entry><entry>5</entry><entry>5</entry></row><row><entry>BaCl₂ (10 mM)</entry><entry>5</entry><entry>5</entry><entry>5</entry><entry>5</entry></row><row><entry>Pefablock (100 mM)</entry><entry>1.3</entry><entry>1.3</entry><entry>1.3</entry><entry>1.3</entry></row><row><entry>Plasma</entry><entry>3.3</entry><entry>3.3</entry><entry>3.3</entry><entry>3.3</entry></row><row><entry>ALX 0081 (2,48 mg/ml)</entry><entry>-</entry><entry>-</entry><entry>4</entry><entry>-</entry></row><row><entry>PBS</entry><entry>-</entry><entry>-</entry><entry>-</entry><entry>4</entry></row><row><entry>EDTA (0.35M) pH=8,3</entry><entry>-</entry><entry>2.6</entry><entry>-</entry><entry>-</entry></row><row><entry>H₂O</entry><entry>81.9</entry><entry>79.3</entry><entry>77.9</entry><entry>77.9</entry></row><row><entry>A1A2A3 (460 g/ml)</entry><entry>3.5</entry><entry>3.5</entry><entry>3.5</entry><entry>3.5</entry></row></tbody></tgroup></table></tables>

PREFERRED EMBODIMENTS

05461. Nanobody against Von Willebrand Factor (vWF), said Nanobody consisting of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: i) CDR1 comprises, essentially consists of, or is an amino acid sequence chosen from the group consisting of: <tables id="tabl0087" num="0087"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="27mm" /><tbody><row><entry>NYGMG</entry><entry>[SEQ ID NO: 15]</entry></row><row><entry>SYTLG</entry><entry>[SEQ ID NO: 16]</entry></row><row><entry>NYNMG</entry><entry>[SEQ ID NO: 17]</entry></row><row><entry>SSAMA</entry><entry>[SEQ ID NO: 18]</entry></row><row><entry>YYNTG</entry><entry>[SEQ ID NO: 19]</entry></row><row><entry>IGAMG</entry><entry>[SEQ ID NO: 20]</entry></row><row><entry>IGTMG</entry><entry>[SEQ ID NO: 21]</entry></row><row><entry>YNPMG</entry><entry>[SEQ ID NO: 22]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0088" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0089" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: ii) CDR2 comprises, essentially consists of or is an amino acid sequence chosen from the group consisting of: <tables id="tabl0088" num="0088"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="44mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>SISWSGTYTAYSDNVKG</entry><entry>[SEQ ID NO: 23]</entry></row><row><entry>GISWSGVSTDYAEFAKG</entry><entry>[SEQ ID NO: 24]</entry></row><row><entry>TSISWSGSYTAYADNVKG</entry><entry>[SEQ ID NO: 25]</entry></row><row><entry>SISWSGMSTYYTDSVKG</entry><entry>[SEQ ID NO: 26]</entry></row><row><entry>TITSGGRTSYADSVKG</entry><entry>[SEQ ID NO: 27]</entry></row><row><entry>AISWSGGLTYYADSVKG</entry><entry>[SEQ ID NO: 28]</entry></row><row><entry>TITSGGSTNYADPVKG</entry><entry>[SEQ ID NO: 29]</entry></row><row><entry>TITSGGSTNYADSVKG</entry><entry>[SEQ ID NO: 30]</entry></row><row><entry>AISRTGGSTYYARSVEG</entry><entry>[SEQ ID NO: 31]</entry></row><row><entry>AISRTGGSTYYPDSVEG</entry><entry>[SEQ ID NO: 32]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0090" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0091" compact="compact"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and in which: iii) CDR3 comprises, essentially consists of or is an amino acid sequence chosen from the group consisting of: <tables id="tabl0089" num="0089"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="47mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><tbody><row><entry>QSRYRSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 33]</entry></row><row><entry>LGRYRSNWRNIGQYDY</entry><entry>[SEQ ID NO: 34]</entry></row><row><entry>QSRYSSNYYDHDDKYAY</entry><entry>[SEQ ID NO: 35]</entry></row><row><entry>SNRYRTHTTQAMYNY</entry><entry>[SEQ ID NO: 36]</entry></row><row><entry>WDGKRAP</entry><entry>[SEQ ID NO: 37]</entry></row><row><entry>NRRQKTVQMGERAYDY</entry><entry>[SEQ ID NO: 38]</entry></row><row><entry>NLKQGSYGYRFNDY</entry><entry>[SEQ ID NO: 39]</entry></row><row><entry>NLKQGDYGYRFNDY</entry><entry>[SEQ ID NO: 40]</entry></row><row><entry>AGVRAEDGRVRTLPSEYNF</entry><entry>[SEQ ID NO: 41]</entry></row><row><entry>AGVRAEDGRVRTLPSEYTF</entry><entry>[SEQ ID NO: 42]</entry></row><row><entry>AGVRAEDGRVRSLPSEYTF</entry><entry>[SEQ ID NO: 43]</entry></row></tbody></tgroup></table></tables> or from the group consisting of amino acid sequences that have at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity (as defined herein) with one of the above amino acid sequences; in which <ol id="ol0092"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s);</li></ol> and/or from the group consisting of amino acid sequences that have 3, 2 or only 1 "amino acid difference(s)" (as defined herein) with one of the above amino acid sequences, in which: <ol id="ol0093"><li>(1) any amino acid substitution is preferably a conservative amino acid substitution (as defined herein); and/or</li><li>(2) said amino acid sequence preferably only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ol> 2. Humanized variant of a Nanobody according to item 1. 3. Nanobody against Von Willebrand Factor (vWF), said Nanobody consisting of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: <ul id="ul0082" list-style="none" compact="compact"><li>g) CDR1 comprises or essentially consists of: <ul id="ul0083" list-style="dash" compact="compact"><li>the amino acid sequence YNPMG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence YNPMG;</li></ul> and</li><li>h) CDR2 comprises or essentially consists of: <ul id="ul0084" list-style="dash" compact="compact"><li>the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> and</li><li>i) CDR3 comprises or essentially consists of: <ul id="ul0085" list-style="dash" compact="compact"><li>the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequences that has only 1 amino acid difference with the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul></li></ul> 4. Nanobody according to item 3, in which CDR1 comprises or essentially consists of the amino acid sequence YNPMG. 5. Nanobody according to item 3, in which CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG 6. Nanobody according to item 3, in which CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF. 7. Nanobody according to item 3, in which: <ul id="ul0086" list-style="dash" compact="compact"><li>CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF</li></ul> 8. Nanobody according to item 3, in which CDR1 comprises or essentially consists of the amino acid sequence YNPMG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF. 9. Nanobody according to item 3, in which CDR1 comprises or essentially consists of the amino acid sequence YNPMG; CDR2 comprises or essentially consists of the amino acid sequence AISRTGGSTYYPDSVEG and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF. 10. Nanobody according to any of items 3-9, in which <ul id="ul0087" list-style="dash" compact="compact"><li>any amino acid substitution is a conservative amino acid substitution; and/or</li><li>said amino acid sequence only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ul> 11. Nanobody against Von Willebrand Factor (vWF), said Nanobody consisting of 4 framework regions (FR1 to FR4 respectively) and 3 complementarity determining regions (CDR1 to CDR3 respectively), in which: <ol id="ol0094" compact="compact"><li>a) CDR1 is: <ul id="ul0088" list-style="dash" compact="compact"><li>the amino acid sequence YNPMG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference with the amino acid sequence YNPMG;</li></ul> and</li><li>b) CDR2 is: <ul id="ul0089" list-style="dash" compact="compact"><li>the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AISRTOGSTYYPDSVEG; or</li><li>an amino acid sequences that has 2 or only 1 amino acid difference(s) with the amino acid sequence AISRTGGSTYYPDSVEG;</li></ul> and</li><li>c) CDR3 is: <ul id="ul0090" list-style="dash" compact="compact"><li>the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequence that has at least 80%, preferably at least 90%, more preferably at least 95%, even more preferably at least 99% sequence identity with the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>an amino acid sequences that has only 1 amino acid difference with the amino acid sequence AGVRAEDGRVRTLPSEYTF.</li></ul></li></ol> 12. Nanobody according to item 11, in which CDR1 is the amino acid sequence YNPMG. 13. Nanobody according to item 11, in which CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG 14. Nanobody according to item 11, in which CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF. 15. Nanobody according to item 11, in which: <ul id="ul0091" list-style="dash" compact="compact"><li>CDR1 is the amino acid sequence YNPMG; and CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF; or</li><li>CDR1 is the amino acid sequence YNPMG; and CDR2 comprises the amino acid sequence AISRTGGSTYYPDSVEG; or</li><li>CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG; and CDR3 comprises the amino acid sequence AGVRAEDGRVRTLPSEYTF</li></ul> 16. Nanobody according to item 11, in which CDR1 is the amino acid sequence YNPMG; and CDR3 comprises or essentially consists of the amino acid sequence AGVRAEDGRVRTLPSEYTF. 17. Nanobody according to item 11, in which CDR1 is the amino acid sequence YNPMG; CDR2 is the amino acid sequence AISRTGGSTYYPDSVEG and CDR3 is the amino acid sequence AGVRAEDGRVRTLPSEYTF. 18. Nanobody according to any of items 11-16, in which <ul id="ul0092" list-style="dash" compact="compact"><li>any amino acid substitution is a conservative amino acid substitution; and/or</li><li>said amino acid sequence only contains amino acid substitutions, and no amino acid deletions or insertions, compared to the above amino acid sequence(s).</li></ul> 19. Nanobody according to any of items 3-18, which is a KERE-class Nanobody. 20. Humanized variant of a Nanobody of any of items 3-19. 21. Nanobody, which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the Nanobodies from the group consisting of SEQ ID NO's 60-73 and SEQ ID NO's 86-97. 22. Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity with at least one of the Nanobodies 12B6 (SEQ ID NO: 62); 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73); 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 23. Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the Nanobodies 12A2 (SEQ ID NO: 71); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 24. Nanobody which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with the Nanobody 12A2H1 (SEQ ID NO: 90). 25. Humanized variant of a Nanobody of any of items 20-24. 26. Nanobody, chosen from the group consisting of the Nanobodies of SEQ ID NO's 60-73 and SEQ ID NO's 86-97. 27. Nanobody, chosen from the group consisting of the Nanobodies 12B6 (SEQ ID NO: 62); 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73); 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 28. Nanobody, chosen from the group consisting of the Nanobodies 12A2 (SEQ ID NO: 71); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 29. Nanobody 12A2H1 (SEQ ID NO:90). 30. Protein or polypeptide, which comprises or essentially consists of a Nanobody according to any of items 1-29. 31. Protein or polypeptide according to item 30, which comprises or essentially consists of at least one Nanobody according to any of items 1-29. 32. Protein or polypeptide according to any of items 30-31, which comprises at least two Nanobodies according to any of items 1-29. 33. Protein or polypeptide according to any of items 30-31, which comprises two Nanobodies according to any of items 1-29. 34. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are Nanobodies according to any of items 3-20. 35. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are Nanobodies according to any of items 22-29. 36. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are Nanobodies according to item 24. 37. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are chosen from the group consisting of the Nanobodies 12B6 (SEQ ID NO: 62); 12A2 (SEQ ID NO: 71); 12F2 (SEQ ID NO: 72); 14H10 (SEQ ID NO: 73); 12B6H1 (SEQ ID NO: 86); 12B6H2 (SEQ ID NO: 87); 12B6H3 (SEQ ID NO: 88); 12B6H4 (SEQ ID NO: 89); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 38. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are chosen from the group consisting of the Nanobodies 12A2 (SEQ ID NO: 71); 12A2H1 (SEQ ID NO: 90); 12A2H3 (SEQ ID NO: 91); 12A2H4 (SEQ ID NO: 92); 12A2H11 (SEQ ID NO: 93) and/or 12A2H13 (SEQ ID NO: 94). 39. Protein or polypeptide according to any of items 30-33, in which the Nanobody or Nanobodies present in the protein or polypeptide are Nanobody 12A2H1 (SEQ ID NO:90). 40. Protein or polypeptide according to any of items: 31-39, which comprises two Nanobodies or at least two Nanobodies, and in which said two or at least two Nanobodies are directly linked to each other or linked to each other via a linker. 41. Protein or polypeptide according to item 40, which comprises two Nanobodies or at least two Nanobodies, and in which said two Nanobodies or at least two Nanobodies are linked to each other via a linker. 42. Protein or polypeptide according to item 41, in which the linker is an amino acid sequence. 43. Protein or polypeptide according to item 42, in which the linker is comprises between 1 and 40 amino acid residues, such as between 2 and 30 amino acid residues. 44. Protein or polypeptide according to item 43, in which the linker comprises or essentially consists of glycine and serine residues. 45. Protein or polypeptide according to item 44, in which the linker comprises the linker GS9 (SEQ ID NO: 84). 46. Protein or polypeptide according to , item 41, in which the linker comprises or essentially consists of alanine residues. 47. Protein or polypeptide according to item 42, in which the linker comprises between 1 and 10 amino acid residues, such as 1, 2, 3, 4 or 5 amino acid residues. 48. Protein or polypeptide, which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the polypeptides from the group consisting of SEQ ID NOS: 74-82 or SEQ ID NOS 98-106. 49. Protein or polypeptide, which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the polypeptides from the group consisting of SEQ ID NOS: 74-76, SEQ ID NO's 80-82 or SEQ ID NOS 98-106. 50. Protein or polypeptide, which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with at least one of the polypeptides from the group consisting of SEQ ID NOS: 74-76 and SEQ ID NOS: 98, 99, 101, 102, 104, 105 and 106. 51. Protein or polypeptide, which has at least 80%, or at least 90%, or at least 95%, or at least 99% sequence identity (as defined herein) with the polypeptides of SEQ ID NO: 90 52. The polypeptide of SEQ ID NO: 90. 53. Fragment of a Nanobody according to any of items 1-29. 54. Fragment of a Nanobody according to any of items 3-20. 55. Fragment of a Nanobody according to any of items 22-29. 56. Fragment of a Nanobody according to item 24. 57. Fragment of a Nanobody according to any of items 27-29. 58. Fragment according to any of items 53-57, which has a degree of sequence identity of at least 50%, preferably at least 60%, more preferably at least 70%, such as at least 80%, at least 90% or at least 95%, with the amino acid sequence of the corresponding full length Nanobody. 59. Protein or polypeptide, which comprises or essentially consists of a fragment according to any of items; 53-58. 60. Protein or polypeptide according to item 59, which comprises or essentially consists of at least one fragment according to any of items 53-58. 61. Protein or polypeptide according to any of items 59 or 60, which comprises at least two fragments according to any of items 53-58. 62. Protein or polypeptide according to any of items 59-61, which comprises two Nanobodies according to any of claims 1-29. 63. Protein or polypeptide according to any of items 59-62, which comprises two fragments or at least two fragments, and in which said two fragments or at least two fragments are directly linked to each other or linked to each other via a linker. 64. Protein or polypeptide, which comprises or essentially consists of a Nanobody that essentially does not inhibit the cleavage of ULvWF by ADAMTS-13. 65. Protein or polypeptide according to item 59, which comprises or essentially consists of at least one Nanobody that essentially does not inhibit the cleavage of ULvWF by ADAMTS-13. 66. Protein or polypeptide according to any of items 59 or 60, which comprises at least two Nanobodies that essentially do not inhibit the cleavage of ULvWF by ADAMTS-13. 67. Protein or polypeptide according to any of items 59-61, which comprises two Nanobodies that essentially do not inhibit the cleavage of ULvWF by ADAMTS-13. 68. Protein or polypeptide according to any of items 64-68, which comprises two fragments or at least two fragments, and in which said two fragments or at least two fragments are directly linked to each other or linked to each other via a linker. 69. Nucleotide sequence or nucleic acid, encoding a Nanobody, protein, polypeptide or fragment according to any of the preceding claims. 70. Host cell, comprising a nucleotide sequence or nucleic acid according to item 64, or which expresses or is capable of expressing a Nanobody, protein, polypeptide or fragment according to any of items 1-68. 71. Method for preparing a Nanobody, protein, polypeptide or fragment according to any of items 1-68, which comprises cultivating or maintaining a host cell according to item 65 under conditions such that said host cell produces or expresses a Nanobody, protein, polypeptide or fragment according to any of items 1-68; and which optionally further comprises isolating the Nanobody, protein, polypeptide or fragment according to any of items 1-68. 72. Pharmaceutical composition, comprising at least one Nanobody, protein, polypeptide or fragment according to any of items 1-68, and optionally at least one pharmaceutically acceptable carrier. 73. A pharmaceutical composition according to item 72, or a Nanobody, protein, polypeptide or fragment according to any of items 1-73, for the prevention or treatment of a disease or disorder related to platelet-mediated aggregation. 74. A pharmaceutical composition according to item 73, or a Nanobody, protein, polypeptide or fragment according to any of items 1-68, for the prevention or treatment of a disease or disorder related to platelet-mediated aggregation, chosen from non-occlusive thrombus, the formation of an occlusive thrombus, arterial thrombus formation, acute coronary occlusion, peripheral arterial occlusive disease, restenosis and disorders arising from coronary by-pass graft, coronary artery valve replacement and coronary interventions such angioplasty, stenting or atherectomy, hyperplasia after angioplasty, atherectomy or arterial stenting, occlusive syndrome in a vascular system or lack of patency of diseased arteries, thrombotic thrombocytopenic purpura (TTP), transient cerebral ischemic attack, unstable or stable angina pectoris, cerebral infarction, HELLP syndrome, carotid endarterectomy, carotid artery stenosis, critical limb ischaemia, cardioembolism, peripheral vascular disease, restenosis and myocardial infarction. 75. A pharmaceutical composition according to item 73, that further contains one or more other active substances for the prevention or treatment of aggregation mediated disorders, such as asperine (Aspegic), heparin, Plavix ® and/or Reopro® 76. Use of a Nanobody, protein, polypeptide or fragment according to any of items: 1-68, in the preparation of a medicament for the prevention or treatment of a disease or disorder related to platelet-mediated aggregation. 77. Use of a Nanobody, protein, polypeptide or fragment according to any of items 1-68, in the preparation of a medicament for the prevention or treatment of a disease or disorder related to platelet-mediated aggregation, chosen from non-occlusive thrombus, the formation of an occlusive thrombus, arterial thrombus formation, acute coronary occlusion, peripheral arterial occlusive disease, restenosis and disorders arising from coronary by-pass graft, coronary artery valve replacement and coronary interventions such angioplasty, stenting or atherectomy, hyperplasia after angioplasty, atherectomy or arterial stenting, occlusive syndrome in a vascular system or lack of patency of diseased arteries, thrombotic thrombocytopenic purpura (TTP), transient cerebral ischemic attack, unstable or stable angina pectoris, cerebral infarction, HELLP syndrome, carotid endarterectomy, carotid artery stenosis, critical limb ischaemia, cardioembolism, peripheral vascular disease, restenosis and myocardial infarction. 78. Use of vWF, of a suitable fragment thereof, of DDAVP (desmopressinor) or a suitable fragment thereof, or of a pharmaceutical composition comprising any of the foregoing, as an antidote for complications or undesired side effects associated with the use of a Nanobody, protein or polypeptide against vWF, in particular of a Nanobody, protein or polypeptide in accordance with any of items 1-68. <img file="EP3415535A1_D0166.tif" /><img file="EP3415535A1_D0167.tif" /><img file="EP3415535A1_D0168.tif" /><img file="EP3415535A1_D0169.tif" /><img file="EP3415535A1_D0170.tif" /><img file="EP3415535A1_D0171.tif" /><img file="EP3415535A1_D0172.tif" /><img file="EP3415535A1_D0173.tif" /><img file="EP3415535A1_D0174.tif" /><img file="EP3415535A1_D0175.tif" /><img file="EP3415535A1_D0176.tif" /><img file="EP3415535A1_D0177.tif" /><img file="EP3415535A1_D0178.tif" /><img file="EP3415535A1_D0179.tif" /><img file="EP3415535A1_D0180.tif" /><img file="EP3415535A1_D0181.tif" /><img file="EP3415535A1_D0182.tif" /><img file="EP3415535A1_D0183.tif" /><img file="EP3415535A1_D0184.tif" /><img file="EP3415535A1_D0185.tif" /><img file="EP3415535A1_D0186.tif" /><img file="EP3415535A1_D0187.tif" /><img file="EP3415535A1_D0188.tif" /><img file="EP3415535A1_D0189.tif" /><img file="EP3415535A1_D0190.tif" /><img file="EP3415535A1_D0191.tif" /><img file="EP3415535A1_D0192.tif" /><img file="EP3415535A1_D0193.tif" /><img file="EP3415535A1_D0194.tif" /><img file="EP3415535A1_D0195.tif" /><img file="EP3415535A1_D0196.tif" /><img file="EP3415535A1_D0197.tif" /><img file="EP3415535A1_D0198.tif" /><img file="EP3415535A1_D0199.tif" /><img file="EP3415535A1_D0200.tif" /><img file="EP3415535A1_D0201.tif" /><img file="EP3415535A1_D0202.tif" /><img file="EP3415535A1_D0203.tif" /><img file="EP3415535A1_D0204.tif" /><img file="EP3415535A1_D0205.tif" /><img file="EP3415535A1_D0206.tif" /><img file="EP3415535A1_D0207.tif" /><img file="EP3415535A1_D0208.tif" /><img file="EP3415535A1_D0209.tif" /><img file="EP3415535A1_D0210.tif" /><img file="EP3415535A1_D0211.tif" /><img file="EP3415535A1_D0212.tif" /><img file="EP3415535A1_D0213.tif" /><img file="EP3415535A1_D0214.tif" /><img file="EP3415535A1_D0215.tif" /><img file="EP3415535A1_D0216.tif" /><img file="EP3415535A1_D0217.tif" /><img file="EP3415535A1_D0218.tif" /><img file="EP3415535A1_D0219.tif" /><img file="EP3415535A1_D0220.tif" /><img file="EP3415535A1_D0221.tif" /><img file="EP3415535A1_D0222.tif" /><img file="EP3415535A1_D0223.tif" /><img file="EP3415535A1_D0224.tif" /><img file="EP3415535A1_D0225.tif" /><img file="EP3415535A1_D0226.tif" /><img file="EP3415535A1_D0227.tif" /><img file="EP3415535A1_D0228.tif" /><img file="EP3415535A1_D0229.tif" /><img file="EP3415535A1_D0230.tif" /><img file="EP3415535A1_D0231.tif" /><img file="EP3415535A1_D0232.tif" /><img file="EP3415535A1_D0233.tif" /><img file="EP3415535A1_D0234.tif" /><img file="EP3415535A1_D0235.tif" /><img file="EP3415535A1_D0236.tif" /><img file="EP3415535A1_D0237.tif" /><img file="EP3415535A1_D0238.tif" /><img file="EP3415535A1_D0239.tif" /><img file="EP3415535A1_D0240.tif" /><img file="EP3415535A1_D0241.tif" /><img file="EP3415535A1_D0242.tif" /><img file="EP3415535A1_D0243.tif" /><img file="EP3415535A1_D0244.tif" /><img file="EP3415535A1_D0245.tif" /><img file="EP3415535A1_D0246.tif" /><img file="EP3415535A1_D0247.tif" /><img file="EP3415535A1_D0248.tif" /><img file="EP3415535A1_D0249.tif" /><img file="EP3415535A1_D0250.tif" /><img file="EP3415535A1_D0251.tif" /><img file="EP3415535A1_D0252.tif" /><img file="EP3415535A1_D0253.tif" /><img file="EP3415535A1_D0254.tif" /><img file="EP3415535A1_D0255.tif" /><img file="EP3415535A1_D0256.tif" /><img file="EP3415535A1_D0257.tif" /><img file="EP3415535A1_D0258.tif" /><img file="EP3415535A1_D0259.tif" /><img file="EP3415535A1_D0260.tif" /><img file="EP3415535A1_D0261.tif" /><img file="EP3415535A1_D0262.tif" /><img file="EP3415535A1_D0263.tif" /><img file="EP3415535A1_D0264.tif" /><img file="EP3415535A1_D0265.tif" /><img file="EP3415535A1_D0266.tif" /><img file="EP3415535A1_D0267.tif" /><img file="EP3415535A1_D0268.tif" /><img file="EP3415535A1_D0269.tif" /><img file="EP3415535A1_D0270.tif" /><img file="EP3415535A1_D0271.tif" /><img file="EP3415535A1_D0272.tif" /><img file="EP3415535A1_D0273.tif" /><img file="EP3415535A1_D0274.tif" /><img file="EP3415535A1_D0275.tif" /><img file="EP3415535A1_D0276.tif" /><img file="EP3415535A1_D0277.tif" />