Nucleic acid amplification primers for pcr-based clonality studies

0001The present invention relates to PCR-based clonality studies for among others early diagnosis of lymphoproliferative disorders. In most patients with suspect lymphoproliferative disorders, histomorphology or cytomorphology supplemented with immunohistology or flow cytometric immunophenotyping can discriminate between malignant and reactive lymphoproliferations. However, in 5 to 10% of cases, making the diagnosis is more complicated. The diagnosis of lymphoid malignancies can be supported by clonality assessment based on the fact that in principle all cells of a malignancy have a common clonal origin.

0002The majority of lymphoid malignancies belongs to the B-cell lineage (90 to 95%) and only a minority belongs to the T-cell lineage (5-7%) or NK-cell lineage (<2%). Acute lymphoblastic leukemias (ALL) are of T-cell origin in 15 to 20% of cases, but in the group of mature lymphoid leukemias and in non-Hodgkin lymphomas (NHL) T-cell malignancies are relatively rare, except for specific subgroups such as cutaneous lymphomas (Table 1). Consequently, the vast majority of lymphoid malignancies (> 98%) contains identically (clonally) rearranged immunoglobulin (Ig) and/or T-cell receptor (TCR) genes and in 25 to 30% of cases also well-defined chromosome aberrations are found, all of which can serve as markers for clonality.^1.2

0003The Ig and TCR gene loci contain many different variable (V), diversity (D), and joining (J) gene segments, which are subjected to rearrangement processes during early lymphoid differentiation.^3.4 The V-D-J rearrangements are mediated via a recombinase enzyme complex in which the RAG1 and RAG2 proteins play a key role by recognizing and cutting the DNA at the recombination signal sequences (RSS), which are located downstream of the V gene segments, at both sides of the D gene segments, and upstream of the J gene segments (<figref idref="f0001">Figure 1</figref>). Inappropriate RSS reduce or even completely prevent rearrangement.

0004The rearrangement process generally starts with a D to J rearrangement followed by a V to D-J rearrangement in case of Ig heavy chain (<i>IGH</i>), TCR beta (<i>TCRB</i>), and TCR delta (<i>TCRD</i>) genes (<figref idref="f0001">Figure 1</figref>) or concerns direct V to J rearrangements in case of Ig kappa (<i>IGK</i>), Ig lambda (<i>IGL</i>), TCR alpha (<i>TCRA</i>), and TCR gamma (<i>TCRG</i>) genes. The sequences between rearranging gene segments are generally deleted in the form of a circular excision product, also called TCR excision circle (TREC) or B cell receptor excision circle (BREC) (<figref idref="f0001">Figure 1</figref>).

0005The Ig and TCR gene rearrangements during early lymphoid differentiation generally follow a hierarchical order. During B-cell differentiation: first the <i>IGH</i> genes rearrange, then <i>IGK,</i> potentially resulting in IgH/κ expression or followed by <i>IGK</i> deletion and <i>IGL</i> rearrangement, potentially followed by IgH/λ expression.⁵ This implies that virtually all Igλ⁺ B-cells have monoallelic or biallelic <i>IGK</i> gene deletions. During T-cell differentiation: first the <i>TCRD</i> genes rearrange, then <i>TCRG,</i> potentially resulting in TCRγδ expression or followed by further <i>TCRB</i> rearrangement and <i>TCRD</i> deletion with subsequent <i>TCRA</i> rearrangement, potentially followed by TCRαβ expression. The Ig and TCR gene rearrangement patterns in lymphoid malignancies generally fit with the above-described hierarchical order, although unusual rearrangement patterns are found as well, particularly in ALL.⁶

0006The many different combinations of V, D, and J gene segments represent the so-called combinatorial repertoire (Table 2), which is estimated to be ∼2x10⁶ for Ig molecules, ∼3x10⁶ for TCRαβ molecules and ∼ 5x10³ for TCRγδ molecules. At the junction sites of the V, D, and J gene segments, deletion and random insertion of nucleotides occurs during the rearrangement process, resulting in highly diverse junctional regions, which significantly contribute to the total repertoire of Ig and TCR molecules, estimated to be >10^12.5

0007Mature B-lymphocytes further extend their Ig repertoire upon antigen recognition in follicle centers via <i>somatic hypermutation</i>, a process, leading to affinity maturation of the Ig molecules. The somatic hypermutation process focuses on the V-(D-)J exon of <i>IGH</i> and Ig light chain genes and concerns single nucleotide mutations and sometimes also insertions or deletions of nucleotides. Somatically-mutated Ig genes are also found in mature B-cell malignancies of follicular or post-follicular origin.⁷

0008Functionally rearranged Ig and TCR genes result in surface membrane expression of Ig, TCRαβ, or TCRγδ molecules. Based on the concept that only a single type of Ig or TCR molecule is expressed by a lymphocyte or lymphocyte clone, the clonally rearranged genes of mature lymphoid malignancies might be detectable at the protein level. Detection of single Ig light chain expression (Igκ or Igλ) has for a long time been used to discriminate between reactive (polyclonal) B-lymphocytes (normal Igκ/Igλ ratio: 0.7 - 2.8) versus aberrant (clonal) B-lymphocytes with Igκ/Igλ ratios of >4.0 or <0.5.^8-10 In the vast majority (>90%) of mature B-cell malignancies, single Ig light chain expression can support the clonal origin of the malignancy.

0009Also, the development of many different antibodies against variable domains of the various TCR chains allows detection of monotypic Vβ, Vγ and Vδ domains, when compared with appropriate reference values.^11-16 In the interpretation of monotypic Vβ results using 20 to 25 antibodies against different Vβ families (Table 2), one should realize that clinically-benign clonal TCRαβ⁺ T-cell expansions (frequently CD8⁺) are regularly found in peripheral blood (PB) of older individuals.^13. " These clonal T-cell expansions in PB are however relatively.small in size: &lt;40% of PB T-lymphocytes and &lt;0.5x10⁶/ml PB.¹³ It is not yet clear to what extent such clinically benign T-cell clones can also be found in lymphoid tissues.

0010The results of monotypic Vγ and Vδ domain expression should be interpreted with caution, because in healthy individuals a large fraction of normal polyclonal TCRγδ⁺ T-lymphocytes has been selected for Vγ9-Jγ1.2 and Vδ2-Jδ1 usage.^18.19 Consequently, high frequencies of Vγ9⁺/Vδ2⁺ T-lymphocytes in PB should be regarded as a normal finding, unless the absolute counts are 1 to 2x10⁶/ml PB. It should be noted that most TCRγδ⁺ T-cell malignancies express Vδ1 or another non-Vδ2 gene segment in combination with a single Vγ domain (generally not Vγ9).^15.20

0011Detection of Igκ or Igλ restricted expression or monotypic Vβ, Vγ or Vδ expression is relatively easy in flow cytometric studies of PB and bone marrow (BM) samples of patients with mature B-cell or T-cell leukemias. However, this appears to be more difficult in tissue samples with suspect lymphoproliferative disorders that are intermixed with normal (reactive) lymphocytes.

0012In contrast to the antibody-based techniques, molecular techniques are broadly applicable for detection of clonally rearranged Ig/TCR genes as well as well-defined chromosome aberrations. This previously concerned Southern blot analysis, but nowadays particularly PCR techniques are used.

0013Difficulties in making a final diagnosis of lymphoid malignancy occur in a proportion of cases (5 to 10%) despite extensive immunophenotyping. Therefore, additional (molecular clonality) diagnostics is needed to generate or to confirm the final diagnosis, such as in case of: <ul id="ul0001" list-style="dash" compact="compact"><li>any suspect B-cell proliferation where morphology and immunophenotyping are not conclusive;</li><li>all suspect T-cell proliferations (CAUTION: T-cell rich B-NHL);</li><li>lymphoproliferations in immunodeficient patients or transplanted patients;</li><li>evaluation of the clonal relationship between two lymphoid malignancies in one patient or discrimination between a relapse and a second malignancy;</li><li>further classification of a malignancy, e.g. via Ig/TCR gene rearrangement patterns or particular chromosome aberrations;</li><li>occasionally: staging of lymphomas.</li></ul>

0014For long time, Southern blot analysis has been the gold standard technique for molecular clonality studies. Southern blotting is based on the detection of non-germline ("rearranged") DNA fragments, obtained after digestion with restriction enzymes. Well-chosen restriction enzymes (resulting in fragments of 2 to 15 kb) and well-positioned DNA probes (particularly downstream J segment probes) allow detection of virtually all Ig and TCR gene rearrangements as well as chromosome aberrations involving J gene segments.^21-28. It should be noted that Southern blot analysis focuses on the rearrangement diversity of Ig/TCR gene segments and therefore takes advantage of the combinatorial repertoire.

0015Optimal Southern blot results for clonality assessment can particularly be obtained with the <i>IGH, IGK,</i> and <i>TCRB</i> genes, because these genes have an extensive combinatorial repertoire as well as a relatively simple gene structure which can be evaluated with only one or two DNA probes.^{22, 24, 28} The <i>IGL</i> and <i>TCRA</i> genes are more complex and require multiple probe sets.^{25, 26, 29} Finally, the <i>TCRG</i> and <i>TCRD</i> genes have a limited combinatorial repertoire, which is less optimal for discrimination between monoclonality and polyclonality via Southern blot analysis.^{20, 21}

0016Despite the high reliability of Southern blot analysis, it is increasingly replaced by PCR techniques, because of several inherent disadvantages: Southern blot analysis is time-consuming, technically demanding, requires 10 to 20 µg of high quality DNA, and has a limited sensitivity of 5 to 10%.²¹

0017Detection of rearranged Ig/TCR genes and chromosome aberrations by PCR techniques requires precise knowledge of the rearranged gene segments in order to design appropriate primers at opposite sides of the junctional regions and breakpoint fusion regions, respectively.

0018In routine PCR-based clonality studies, the distance between the primers should be less than 1 kb, preferably less than 500 bp. This is particularly important for discrimination between PCR products from monoclonal versus polyclonal Ig/TCR gene rearrangements, which is based on the diversity of the junctional regions (diversity in size and composition). So far, mainly <i>IGH</i> and <i>TCRG</i> gene rearrangements have been used for PCR-based clonality studies, because of the limited number of primers needed to detect V_H-J_H and Vγ-Jγ rearrangements.

0019The main advantages of PCR techniques are their speed, the low amounts of DNA required, the possibility to use DNA of lower quality, and the relatively good sensitivity of 1 to 5%, for some types of rearrangements even &lt;1%. Consequently, PCR techniques allow the use of small biopsies (e.g. fine needle aspiration biopsies), or the use of formaldehyde-fixed paraffin-embedded samples, which generally results in DNA of lower quality. Therefore also archival material might be used, if needed.

0020<patcit id="pcit0001" dnum="WO0200848A"><text>WO 02/00848</text></patcit> discloses a PCR-based method for detecting V_H-J_H rearrangements, see in particular the primers VH₃ and VLJH. Molecular clonality studies can be highly informative, but several limitations and pitfalls might hamper the interpretation of the results obtained with conventional detection methods:

1.

Limited sensitivity, related to normal polyclonal background

0021The detection limit varies between 1% and 10% (or even 15%), dependent on the applied technique (Southern blot analysis or PCR techniques) and dependent on the relative size of the "background" of normal (polyclonal) B- and T-lymphocytes. A limited sensitivity might hamper the detection of small clonal cell populations with less than 5 to 10% clonal lymphoid cells.

2.

Clonality is not equivalent to malignancy

0022Detection of clonality does not always imply the presence of a malignancy. Some clinically benign proliferations have a clonal origin, such as many cases of CD8⁺ (or sometimes CD4⁺) T-lymphocytosis, benign monoclonal gammopathies, initial phases of EBV⁺ lymphoproliferations (frequently being oligoclonal) in immunodeficient patients, and benign cutaneous T-cell proliferations, such as lymphomatoid papulosis, etc. This implies that results of molecular clonality studies should always be interpreted in the context of the clinical, morphological, and immunophenotypic diagnosis, i.e. in close collaboration with hematologists, cytomorphologists, pathologists and immunologists.

3.

Ig and TCR gene rearrangements are not markers for lineage

0023In contrast to the initial assumption, it is now clear for more than a decade that Ig and TCR gene rearrangements are not necessarily restricted to B-cell and T-cell lineages, respectively. Cross-lineage TCR gene rearrangements occur relatively frequently in immature B-cell malignancies, particularly in precursor-B-ALL (>90% of cases),³⁰ but also acute myeloid leukemias (AML) and mature B-cell malignancies might contain TCR gene rearrangements.^31-33 Albeit at a lower frequency, also cross-lineage Ig gene rearrangement occur in T-cell malignancies and AML, mainly involving the Ig heavy chain (<i>IGH</i>) locus.^{33, 34} Virtually all (>98%) TCRαβ⁺ T-cell malignancies have <i>TCRG</i> gene rearrangements (generally biallelic) and many TCRγδ⁺ T-cell malignancies have <i>TCRB</i> gene rearrangements, implying that the detection of <i>TCRB</i> or <i>TCRG</i> rearrangements is not indicative of T-cells of the αβ or γδ T-cell lineage, respectively, either. In addition to these cross-lineage rearrangements, it has been established that several lymphoid malignancies have unusual Ig/TCR gene rearrangement patterns. This information is available in detail for precursor-B-ALL and T-ALL, but not yet for most other lymphoid malignancies.⁶

4.

Pseudoclonality and oligoclonality

0024The detection of a seemingly clonal or seemingly oligoclonal lymphoid cell population (pseudoclonality) is rare in Southern blot analysis, unless genes with a limited combinatorial repertoire are used, such as <i>TCRG</i> or <i>TCRD.</i> This might result in faint rearranged bands, e.g. representing Vγ9-Jγ1.2 or Vδ2-Jδ1 rearrangements derived from antigen-selected TCRγδ⁺ T-lymphocytes. Yet, this is a well-known pitfall of Southern blot analysis and will not result in rearranged bands of high density.

0025Pseudoclonality in PCR-based clonality studies is more difficult to recognize. The high sensitivity of PCR can cause amplification of the few Ig or TCR gene rearrangements derived from a limited number of B-cells or T-cells in the studied tissue sample. Particularly the few reactive (polyclonal) T-cells in a small needle biopsy or in a B-NHL sample with high tumor load might result in (oligo)clonal PCR products. Frequently the amount of such PCR products is limited. This is particularly seen when <i>TCRG</i> genes are used as PCR target. Duplicate or triplicate PCR analyses followed by mixing of the obtained PCR products should help to clarify whether the seemingly clonal PCR products are in fact derived from different lymphocytes.

0026Finally, reactive lymph nodes can show a reduced diversity of the Ig/TCR repertoire, caused by predominance of several antigen-selected subclones (oligoclonality). Particularly lymph nodes or blood samples of patients with an active EBV or CMV infection can show a restricted TCR repertoire or TCR gene oligoclonality. Also clinical pictures of immunosuppression are frequently associated with restricted TCR repertoires, e.g. in transplant patients or patients with hairy cell leukemia.³⁵ Recovery from transplantation and hematological remission are followed by restoration of the polyclonal TCR repertoire. ^{36, 37}

5. False-positive results

0027In Southern blot analysis, false-positive results are rare and can generally be prevented by checking for underdigestion and by excluding polymorphic restriction sites.²¹

0028False-positive PCR results comprise a serious problem, if no adequate analysis of the obtained PCR products is performed to discriminate between monoclonal or polyclonal PCR products. Such discrimination can be achieved via single-strand conformation polymorphism (SSCP) analysis,³⁸ denaturing gradient gel electrophoresis (DGGE),³⁹ heteroduplex analysis (HD),^{40, 41} or GeneScanning (GS).^{42, 43} These techniques exploit the junctional region diversity for discrimination between monoclonal cells with identical junctional regions and polyclonal cells with highly diverse junctional regions.

6.

False-negative results

0029False-negative results are rare in Southern blot analysis if appropriate J gene segment probes are used. Nevertheless, some uncommon rearrangements (generally non-functional rearrangements) might be missed, such as V-D rearrangements or deletions of the J regions. PCR analysis of Ig and TCR genes might be hampered by false-negative results because of improper annealing of the applied PCR primers to the rearranged gene segments. This improper primer annealing can be caused by two different phenomena. Firstly, precise detection of all different V, D, and J gene segments would require many different primers (Table 1), which is not feasible in practice. Consequently, family primers are designed, which specifically recognize most or all members of a particular V, D, or J family. Alternatively, consensus primers are used, which are assumed to recognize virtually all V and J gene segments of the locus under study. Family primers and particularly consensus primers are generally optimal for a part of the relevant gene segments, but show a lower homology (70 to 80%) to other gene segments. This may eventually lead to false-negative results, particularly in Ig/TCR genes with many different gene segments. In <i>TCRG</i> and <i>TCRD</i> genes this problem is minimal, because of their limited number of different gene segments. The second phenomenon is the occurrence of somatic hypermutations in rearranged Ig genes of follicular and post-follicular B-cell malignancies, particularly B-cell malignancies with class-switched <i>IGH</i> genes.

0030Sufficient knowledge and experience can prevent the first four pitfalls, because they mainly concern interpretation problems. The last two pitfalls concern technical problems, which can be solved by choosing reliable techniques for PCR product analysis and by the design of better primer sets.

0031Optimization of Southern blot analysis of Ig/TCR genes during the last ten years has resulted in the selection of reliable combinations of restriction enzymes (fragments between 2 and 15 kb, avoiding polymorphic restriction sites) and probes (mainly downstream of J gene segments). Although Southern blot analysis is a solid "gold standard" technique, many laboratories have gradually replaced Southern blot analysis by PCR technology, because PCR is fast, requires minimal amounts of medium-quality DNA, and has an overall good sensitivity.

0032Despite the obvious advantages, replacement of Southern blot analysis by PCR techniques for reliable Ig/TCR studies is hampered by two main technical problems: <ul id="ul0002" list-style="dash" compact="compact"><li>false negative results due to improper primer annealing;</li><li>difficulties in discrimination between monoclonal and polyclonal Ig/TCR gene rearrangements.</li></ul>

0033Several individual diagnostic laboratories tried to solve the problems of the PCR-based clonality studies, but thus far no reliably standardized PCR protocols were obtained. In contrast, many different primer sets are being used, which all differ in their sensitivity and applicability.

0034The present invention now discloses sets of nucleic acid amplification primers and standardized PCR protocols for detecting essentially all relevant Ig and TCR loci and two frequently occurring chromosome aberrations. The primers sets according to the invention comprising a forward and a reverse primer are capable of amplifying clonal rearrangements of the Ig heavy chain genes (<i>IGH</i>). Further, primers capable of amplifying rearrangements of Ig kappa chain genes (<i>IGK</i>), Ig lamba chain genes (<i>IGL</i>), TCR beta genes (<i>TCRB</i>), TCR gamma genes (<i>TCRG</i>), and TCR delta genes (<i>TCRD</i>) or of amplifying chromosomal translocation t(11;14)(<i>BCL1-IGH</i>) and t(14;18)(<i>BCL2-IGH</i>) are disclosed. The primers allow that both complete and incomplete rearrangements are detectable and that gene segments from different V, (D), and J families can be recognized.

0035Two techniques which can be used in a method of the invention for discrimination between monoclonal and polyclonal Ig/TCR gene rearrangements are heteroduplex analysis and GeneScanning. Heteroduplex analysis uses double-stranded PCR products and takes advantage of the length and composition of the junctional regions, whereas in GeneScanning single-stranded PCR products are separated in a high-resolution gel or polymer according to their length only (<figref idref="f0002">Figure 2</figref>).

0036107 different, specific primers for all the relevant Ig/TCR loci as well as for t(11;14) (<i>BCL1-IGH</i>) and t(14;18) (<i>BCL2-IGH</i>) are provided (see <figref idref="f0004 f0005 f0006 f0007 f0008 f0009 f0010 f0011 f0012 f0013 f0014">Figures 3 to 11</figref>). In addition, a primer may comprise a (differentially) labeled primer, i.e. a primer having a label that can be identified or distinguished from other labels by any means, including the use of an analytical instrument. Examples of differentially labeled primers are primers provided with a fluorescent label such as a 6-FAM, HEX, TET or NED dye. Labeled primers are particularly advantageous for use in automated high resolution PCR fragment analysis (Gene Scanning technology) for detection of PCR products. As is exemplified below, differentially labeled primers allow to distinguish different PCR amplification products of approximately the same length (size), preferably using multi-color GeneScanning. Of course, a nucleic acid amplification primer, be it a forward or a reverse (dye-labeled) primer, should not be capable of forming dimers with any other forward and/or reverse nucleic acid amplification primer that is used in an amplification reaction, since this can interfere with primer annealing to a target locus and thus with the amplification of the rearrangement or translocation of interest.

0037In one embodiment, the invention provides a nucleic acid amplification assay, preferably a PCR assay, using at least one set of primers according to the invention. Said PCR assay can be a single (monoplex) or a multiplex PCR. In a preferred embodiment, a set of primers according to the invention is used in a standardized multiplex PCR assay, using for example two or more forward primers, or three or four forward primers, together with one or more consensus reverse primer(s), . The family primers of the invention are designed in such a way that they recognize most or all gene segments of a particular family (see Table 2). In a specific embodiment, all 107 primers are used in only 18 multiplex PCR tubes: 5 for <i>IGH</i> (3x V_H-J_H and 2x D_H-J_H), 2 for <i>IGK,</i> 1 for <i>IGL,</i> 3 for <i>TCRB</i> (2x Vβ-Jβ and 1x Dβ-Jβ), 2 for <i>TCRG,</i> 1 for <i>TCRD,</i> 3 for <i>BCL2-IGH</i>, and 1 for <i>BCL1-IGH</i> (<figref idref="f0004 f0005 f0006 f0007 f0008 f0009 f0010 f0011 f0012 f0013 f0014">Figures 3 to 11</figref>). Such an assay allows assessing clonal rearrangements and / or chromosome aberrations. Furthermore, it allows detection of a lymphoproliferative disorder. Multiplex PCR testing of the primers on about 90 Southern blot defined lymphoproliferations showed that in more than 95% of the samples the Southern blot and PCR results were concordant.

0038In another embodiment, a method is provided for detecting a rearrangement, preferably two or more rearrangements consisting of a V_H-J_H<i>IGH</i> rearrangement and optionally a D_H-J_H<i>IGH</i> rearrangement, a Vκ-Jκ <i>IGK</i> rearrangement, a Vκ/intron-Kde <i>IGK</i> rearrangement, a Vλ-Jλ <i>IGL</i> rearrangement, a Vβ-Jβ <i>TCRB</i> rearrangement, a Dβ-Jβ <i>TCRB</i> rearrangement, a V_Y-J_Y<i>TCRG</i> rearrangement, a Vδ-Jδ <i>TCRD</i> rearrangement, a Dδ-Jδ <i>TCRD</i> rearrangement, a Dδ-Dδ <i>TCRD</i> rearrangement, and a Vδ-Dδ <i>TCRD</i> rearrangement, using at least one set of primers according to the invention. The method may encompass detecting a t (11;14)(<i>BCL1-IGH</i>) translocation or a t(14;18)(<i>BCL2-IGH</i>) translocation.

0039Furthermore, methods are disclosed for detecting at least one of the above rearrangements and at least one translocation, using at least two sets of primers as provided herein.

0040A set of nucleic acid amplification primers capable of amplifying a human gene selected from the group consisting of the human <i>AF4</i> gene (exon 3), the human AF4 gene (exon 11), the human <i>PLZF1</i> gene, the human <i>RAG1</i> gene and the human <i>TBXAS1</i> gene are disclosed (see <figref idref="f0015">Fig. 12</figref>). Using one or more of these five primer sets consisting of a forward primer and a reverse primer in a nucleic acid amplification assay of the invention, it is possible to detect one or more "Control Gene(s)" selected from the group consisting of the human AF4 gene (exon 3), the human <i>AF4</i> gene (exon 11), the human <i>PLZF1</i> gene, the human <i>RAG1</i> gene and the human <i>TBXAS1</i> gene. Such a detection method is advantageously used to assess the quality (e.g. integrity and amplifiability) of a nucleic acid (DNA) sample extracted or isolated from a biological sample, for instance DNA extracted from a paraffin-embedded sample (see Example 10).

0041The ability of the different primer sets to amplify clonal rearrangements and/ or chromosomal aberrations (translocations) has been tested in many different types of malignant lymphomas, among which follicular lymphoma, diffuse large B-cell lymphoma, and multiple myeloma. It was found that a set of primers is very useful for assessing clonal rearrangements and/or chromosomal translocations. It appeared that the detection rate of clonal rearrangements using the multiplex primer tubes according to the invention is unprecedentedly high, i.e at least 95%.

0042Parallel testing of available paraffin-embedded tissues of the above samples revealed largely identical results, if the DNA quality of these tissues is sufficiently high, meaning that fragments of at least 300 bp can be amplified in a specially-designed control gene PCR.

0043The applicability of the developed multiplex PCR assays according to the invention was evaluated on series of 50 to 100 cases per type of lymphoid malignancy. Following national pathology panel review, and central pathology panel review in case of difficulties, all included cases were defined according to the World Health Organization (WHO) classification. The studied diagnostic categories included malignancies such as follicular lymphoma, mantle cell lymphoma, marginal zone lymphoma, diffuse large B-cell lymphoma, angioimmunoblastic T-cell lymphoma, peripheral T-cell lymphoma, and anaplastic large cell lymphoma, as well as reactive lesions. The results show a very high level of clonality detection, even in entities, which are known to bear somatic hypermutations such as follicular lymphoma and diffuse large B-cell lymphoma. Particularly the usage of the three <i>IGH</i> V_H-J_H tubes, supplemented with the two <i>IGH</i> D_H-J_H tubes and the two <i>IGK</i> tubes appeared to be highly efficient in the detection of clonal Ig gene rearrangements. This high efficiency is obtained by the complementarity of the Ig tubes as well as by the fact that D_H-J_H and <i>IGK</i>-Kde rearrangements are not (or rarely) somatically mutated. Such complementarity was also found for the <i>TCRB</i> and <i>TCRG</i> primers in case of T-cell malignancies.

0044Furthermore, interesting and unexpected rearrangement patterns, such as unusual cross-lineage rearrangements, were observed. Remarkably, in about 10% of reactive lesions clonal rearrangements were detected. These reactive lymphoproliferations included EBV-related lymphoproliferations and atypical hyperplasias like Castleman's disease, as well as lesions that were suspicious for a B- or T-cell clone.

0045In a specific embodiment, a method is provided for the detection of minimal residual disease (MRD). The term minimal residual disease (MRD) describes the situation in which, after chemotherapy for acute leukemia (AL), a morphologically normal bone marrow can still harbor a relevant amount of residual malignant cells. Detection of minimal residual disease (MRD) is a new practical tool for a more exact measurement of remission induction during therapy because leukemic blasts can be detected down to 10^-4-10^-6. Known PCR-based MRD analysis uses clonal antigen receptor rearrangements detectable in ∼90-95% of the investigated patient samples. However, amplification of polyclonal products often leads to false-positive PCR amplicons not suitable for MRD analysis. The method for the detection of identically (clonally) rearranged Ig and TCR genes or detection of well-defined and frequent chromosome aberrations, such as t(11;14), and t(14;18) is disclosed. Thus, the rearrangements and translocations detected using a set of primers of the invention not only serve as markers for clonality at diagnosis, but also as PCR targets for detection of MRD during follow-up.

0046In a further aspect, the invention provides a (diagnostic) kit for the detection of at least a V_H-J_H<i>IGH</i> rearrangement and optionally a D_H-J_H<i>IGH</i> rearrangement, a Vκ-Jκ IGK rearrangement, a Vκ/intron-Kde <i>IGK</i> rearrangement, a Vλ-Jλ <i>IGL</i> rearrangement, a Vβ-Jβ <i>TCRB</i> rearrangement, a Dβ-Jβ <i>TCRB</i> rearrangement, a V_Y-J_Y<i>TCRG</i> rearrangement, a Vδ-Jδ <i>TCRD</i> rearrangement, a Dδ-Jδ <i>TCRD</i> rearrangement, a Dδ-Dδ <i>TCRD</i> rearrangement, a Vδ-Dδ <i>TCRD</i> rearrangement and/or at least one translocation selected from t(11;14)(<i>BCL1-IGH</i>) and t(14;18)(<i>BCL2-IGR</i>), comprising at least one set of primers according to the invention. A kit of the invention is highly suitable for PCR-based clonality diagnostics. Optionally, such a kit also comprises at least one set of primers capable of amplifying a human "control gene" as mentioned above. Inclusion of one, preferably at least two, more preferably at least three of these control gene primer sets in a Control Tube can be helpful in estimating the quality of the DNA sample to be diagnosed, for instance DNA extracted from paraffin-embedded tissue.

0047In a further aspect, the invention provides a method for rapid discrimination of different types of Ig/TCR gene rearrangements in the same multiplex PCR tube. GeneScanning allows the application of multiple different fluorochrome-conjugated primers in a single tube. Such differential labeling of primers can be used for extra discrimination between different types of Ig or TCR gene rearrangements.

0048Differential labeling of V primers generally has limited added value, but differential labeling of downstream primers can support the rapid and easy identification of the type of Ig/TCR gene rearrangement, which is useful for PCR-based detection of minimal residual disease.^44.45 Labeling of J primers is not regarded to be informative for <i>IGH</i> (V_H-J_H or D_H-J_H), IGK (Vκ-Jκ), or IGL (Vλ-Jλ). For rapid identification of <i>IGK</i>-Kde rearrangements, it might be interesting to discriminate between Vκ-Kde and intron RSS-Kde rearrangements by differential labeling of the Kde and intron RSS primers (see <figref idref="f0006">Figure 5B</figref>).

0049The most informative multicolor GeneScanning can be designed for TCR gene rearrangements, facilitating the rapid recognition of the different types of <i>TCRB, TCRG,</i> and <i>TCRD</i> gene rearrangements. For example, differential labeling of the Jβ1 and Jβ2 primers in <i>TCRB</i> tube A (see <figref idref="f0009">Figure 7B</figref>) allows easy identification of the polyclonal and monoclonal Vβ-Jβ1 versus Vβ-Jβ2 rearrangements (<figref idref="f0016">Figure 13A</figref>). Differential labeling of the Jγ1.3/2.3 and Jγ1.1/2.1 primers (<figref idref="f0011">Figure 8B</figref>) results in easy identification of the different types of <i>TCRG</i> gene rearrangements (<figref idref="f0016">Figure 13B</figref>). Differential labeling of the Jδ primers, Dδ2 primer, and Dδ3 primer in the <i>TCRD</i> tube (<figref idref="f0012">Figure 9B</figref>) results in easy identification of the most relevant <i>TCRD</i> gene rearrangements, such as Dδ2-Jδ, Vδ-Jδ, Dδ2-Dδ3, and Vδ2-Dδ3 rearrangements (<figref idref="f0016">Figure 13C</figref>).

0050These multi-color multiplex PCR tubes appear to be easy and convenient in daily practise of PCR based clonality diagnotics.

LEGENDS TO THE FIGURES

0051<figref idref="f0001"><b>Figure 1</b></figref><b>. Schematic diagram of sequential rearrangement steps, transcription, and translation of the <i>TCRB</i> gene.</b> In this example first a Dβ2 to Jβ2.3 rearrangement occurs, followed by Vβ4 to Dβ2-Jβ2.3 rearrangement, resulting in the formation of a Vβ4-Dβ2-Jβ2.3 coding joint. The rearranged <i>TCRB</i> gene is transcribed into precursor mRNA, spliced into mature mRNA, and finally translated into a TCRβ protein chain. The two extrachromosomal TCR excision circles (TRECs) that are formed during this recombination process are indicated as well; they contain the D-J signal joint and V-D signal joint, respectively.

0052<figref idref="f0002"><b>Figure 2</b></figref><b>. Schematic diagram of heteroduplex analysis and GeneScanning of PCR products, obtained from rearranged Ig and TCR genes. A.</b> Rearranged Ig and TCR genes (<i>IGH</i> in the example) show heterogeneous junctional regions with respect to size and nucleotide composition. Germline nucleotides of V, D, and J gene segments are given in large capitals and randomly inserted nucleotides in small capitals. The junctional region heterogeneity is employed in heteroduplex analysis (size and composition) and GeneScanning (size only) to discriminate between products derived from monoclonal and polyclonal lymphoid cell populations. <b>B.</b> In heteroduplex analysis, PCR products are heat-denatured (5 min, 94°C) and subsequently rapidly cooled (1 hour, 4°C) to induce duplex (homo- or heteroduplex) formation. In cell samples consisting of clonal lymphoid cells, the PCR products of rearranged <i>IGH</i> genes give rise to homoduplexes after denaturation and renaturation, whereas in samples which contain polyclonal lymphoid cell populations the single-strand PCR fragments will mainly form heteroduplexes, which result in a background smear of slowly migrating fragments upon electrophoresis. <b>C.</b> In GeneScanning fluorochrome-labeled PCR products of rearranged <i>IGH</i> genes are denatured prior to high-resolution fragment analysis of the resulting single-stranded fragments. Monoclonal cell samples will give rise to PCR products of identical size (single peak), whereas in polyclonal samples many different <i>IGH</i> PCR products will be formed, which show a characteristic Gaussian size distribution.

0053<figref idref="f0003 f0004"><b>Figure 3</b></figref><b>. PCR analysis of <i>IGH</i> (VH-JH) rearrangements. A.</b> Schematic diagram of <i>IGH</i> gene complex on chromosome band 14q32.3 (adapted from ImMunoGeneTics database). ^{46, 47} Only rearrangeable non-polymorphic VH gene segments are included in blue (functional VH), or in gray (rearrangeable pseudogenes). Recently discovered (generally truncated) VH pseudogenes are not indicated. <b>B.</b> Schematic diagram of <i>IGH</i> VH-JH rearrangement with three sets of VH primers and one JH consensus primer, combined in three multiplex tubes. The relative position of the VH and JH primers is given according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. The VH gene segment used as representative VH family member for primer design is indicated in parentheses. <b>C, D, and E</b>. Heteroduplex analysis and GeneScanning of the same polyclonal and monoclonal cell populations, showing the typical heteroduplex smears and homoduplex bands (left panels) and the typical polyclonal Gaussian curves and monoclonal peaks (right panels). The approximate distribution of the polyclonal Gaussian curves is indicated in nt.

0054<figref idref="f0005"><b>Figure 4</b></figref><b>. PCR analysis of <i>IGH</i> (D_H-J_H) rearrangements. A.</b> Schematic diagram of <i>IGH</i> (D_H-J_H) rearrangement with seven DH family primers and one JH consensus primer, divided over two tubes (<i>IGH</i> tubes D and E). The D_H7 (7-27) primer was separated from the other six DH primers, because the DH7 and JH consensus primer will give a germline PCR product of 211 nt. The relative position of the DH and JH primers is given according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. The D_H gene segment used as representative D_H family member for primer design is indicated in parentheses. <b>B and C.</b> Heteroduplex analysis (left panels) and GeneScanning (right panels) of the same polyclonal and monoclonal cell populations. The approximate distribution of the polyclonal and monoclonal peaks is indicated. The potential background band/peak in tube D is indicated with an asterisk and is located outside the expected range of D_H-J_H rearrangements. The germline D_H7-J_H band of tube E is also indicated with an asterisk.

0055<figref idref="f0006 f0007"><b>Figure 5</b></figref><b>. PCR analysis of <i>IGK</i> gene rearrangements. A.</b> Schematic diagram of the <i>IGK</i> gene complex on chromosome band 2p 11.2 (adapted from ImMunoGeneTics database).^46.47 Only rearrangeable non-polymorphic Vκ gene segments are indicated in blue (functional Vκ) or in grey (nonfunctional Vκ). The cluster of inverted Vκ gene segments (coded with the letter D) is located ∼800 kb upstream of the non-inverted Vκ gene segments. These upstream Vκ gene segments are presented as a mirrored image to their corresponding non-inverted counterparts. <b>B.</b> Schematic diagrams of Vκ-Jκ rearrangement and the two types of Kde rearrangements (Vk-Kde and intron RSS-Kde). The relative position of the Vκ, Jκ, Kde and intron RSS (INTR) primers is given according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. The Vκ gene segment used as representative member of the Vκ1, Vκ2, and Vκ3 families are indicated in parentheses. Vκ4, Vκ5, and Vκ7 are single-member Vκ families. The primers are divided over two tubes: tube A with Vκ and Jκ primers and tube B with Vκ, intron RSS, and Kde primers. <b>C and D</b>. Heteroduplex analysis and GeneScanning of the same polyclonal and monoclonal cell populations, showing the typical heteroduplex smears and homoduplex bands (left panels) and the typical Gaussian curves and monoclonal peaks (right panels). The approximate distribution of the polyclonal Gaussian curves is indicated in nt.

0056<figref idref="f0008"><b>Figure 6</b></figref><b>. PCR analysis of <i>IGL</i> gene rearrangements. A</b>. Schematic diagram of <i>IGL</i> gene complex on chromosome band 22q11.2 (adapted from ImMunoGenetics database).^46. " Only rearrangeable non-polymorphic Vλ gene segments are included in blue (functional Vλ) or in grey (nonfunctional Vλ) B. Schematic diagram of Vλ-Jλ rearrangement with two Vλ family primers and one Jλ consensus primer. Only two Vλ primers were designed for Vλ1 plus Vλ2 and for Vλ3, because these three Vλ families cover approximately 70% of rearrangeable Vλ gene segments and because approximately 90% of all <i>IGL</i> gene rearrangements involve Vλ1, Vλ2, or Vλ3 gene segments. ⁴⁸ Although five of the seven Jλ gene segments can rearrange, only a single Jλ consensus primer was designed for Jλ1, Jλ2, and Jλ3, because 98% of all <i>IGL</i> gene rearrangements involve one of these three gene segments. ⁴⁹ The relative position of the Vλ and Jλ primers is given according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. <b>C</b>. Heteroduplex analysis and GeneScanning of the same polyclonal and monoclonal cell populations, showing the typical heteroduplex smears and homoduplex bands (left panel) and the polyclonal Gaussian curves and monoclonal peaks (right panel). The approximate position of the polyclonal Gaussian curves is indicated in nt.

0057<figref idref="f0009 f0010"><b>Figure 7</b></figref><b>. PCR analysis of TCRB gene rearrangements. A</b>. Schematic diagram of the human <i>TCRB</i> locus. The gene segment designation is according to Arden et al. ⁵⁰ with the designation according to Rowen et al. ⁵¹ and Lefranc et al. ^{46, 47} in parentheses. The figure is adapted from the international ImMunoGeneTics database. ^{46, 47} Only the rearrangeable non-polymorphic Vβ gene segments are depicted in blue (functional Vβ), in half blue/half gray (potential functional, but no protein expression found) and in grey (non-functional Vβ). <b>B.</b> Schematic diagram of Vβ-Jβ and Dβ-Jβ rearrangements. The 23 Vβ primers, 13 Jβ primers and two Dβ primers are combined in three tubes: tube A with 23 V primers and nine Jβ primers, tube B with 23 Vβ primers and four Jβ primers, and tube C with two Dβ primers and 13 Jβ primers. The 23 Vβ primers and the 13 Jβ primers are aligned in order to obtain comparably sized PCR products (see panels C and D). The Vβ primers cover approximately 90% of all Vβ gene segments. The relative position of the Vβ, Dβ, and Jβ primers is given according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. <b>C, D, and E</b>. Heteroduplex analysis and GeneScanning of the same polyclonal and monoclonal cell populations, showing the typical heteroduplex smears and homoduplex bands (left panels) and the typical polyclonal Gaussian curves and monoclonal peaks (right panels). The approximate distribution of the polyclonal Gaussian curves is indicated in nt.

0058<figref idref="f0011"><b>Figure 8</b></figref><b>. PCR analysis of <i>TCRG</i> gene rearrangements. A.</b> Schematic diagram of the human <i>TCRG</i> locus on chromosome band 7p14. Only the rearrangeable Vγ gene segments are depicted in blue (functional Vγ) or in gray (non-functional Vγ). For the Jγ gene segments, both nomenclatures are used. ^46.47.52<b>B</b>. Schematic diagram of TCRG Vγ-Jγ rearrangement with four Vγ primers and two Jγ primers, which are divided over two tubes. The relative position of the Vγ and Jγ primers is indicated according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. <b>C and D.</b> Heteroduplex analysis and GeneScanning of the same polyclonal and monoclonal cell populations, showing the typical heteroduplex smears and homoduplex bands (left panels) and the typical polyclonal Gaussian curves and monoclonal peaks (right panels). The approximate distribution of the polyclonal Gaussian curves is indicated in nt.

0059<figref idref="f0012"><b>Figure 9</b></figref><b>. PCR analysis of <i>TCRD</i> gene rearrangements</b>. <b>A.</b> Schematic diagram of human <i>TCRD</i> locus on chromosome band 14q11.2. The six "classical" Vd gene segments are indicated in blue, scattered between the Vα gene segments in black. Since Vδ4, Vδ5, and Vδ6 are also recognized as Vα gene segments, their Vα gene code is given in parenthesis. <b>B.</b> Schematic diagram of Vδ-Jδ, Dδ2-Jδ, Dδ2-Dδ3, and Vδ-Dδ3 rearrangements, showing the positioning of six Vδ, four Jδ, and two Dδ primers, all combined in a single tube. The relative position of the Vδ, Dδ, and Jδ primers is indicated according to their most 5' nucleotide upstream (-) or downstream (+) of the involved RSS. C. Heteroduplex analysis (left panel) and GeneScanning (right panel) of the same polyclonal and monoclonal cell populations. The polyclonal cell populations show a vague smear in heteroduplex analysis and a complex and broad peak pattern in GeneScanning. The monoclonal bands and peaks are clearly visible. The approximate position of the PCR products of the different types of rearrangements in GeneScanning is indicated.

0060<figref idref="f0013"><b>Figure 10</b></figref><b>. Detection of <i>BCL1</i>-IGH rearrangements. A.</b> Schematic diagram of the <i>CCND1</i> gene and the <i>BCL1</i> breakpoint region MTC on chromosome band 11q13 as well as the J_H gene segment on chromosome band 14q32. For the primer design in the <i>BCL1-</i>MTC region an artificial <i>BCL1</i>-MTC/JH4 junctional sequence was composed (as partially reported for JVM2⁵³): the first 50-nucleotides as reported by Williams⁵⁴ were linked to nucleotide 1-439 from MTC-sequence present at NCBI (accession-number S77049 ⁵⁵); the N-region "GCCC" of JVM2⁵³ was added followed by nucleotide 1921-3182 representing the JH4-JH6 genomic region (accession-number J00256). <b>B.</b> Agarose gel electrophoresis of a series of <i>BCL1</i>-IGH PCR products from different MCL patients and the positive control cell line JVM2. The PCR products differ is size, indicating different positions of the <i>BCL1</i>-MTC breakpoints. The larger bands of lower density represent PCR products that extend to the next downstream germline JH gene segment.

0061<figref idref="f0014"><b>Figure 11</b></figref><b>. PCR detection of <i>BCL2</i>-IGH rearrangements. A.</b> Schematic diagram of the <i>BCL2</i> gene on chromosome band 18q21. The majority of the <i>BCL2</i> breakpoints cluster in three regions: MBR, 3' MBR, and mcr. Consequently, multiplex primers have been designed to cover the potential breakpoints in these three regions: two MBR primers, four 3' MBR primers, and three mcr primers. The relative position of the <i>MCL2</i> primers is indicated according to their most 5' nucleotide upstream (-) or downstream (+) to the 3' end of <i>BCL2</i> exon 3 (according to NCBI accession no. AF325194S1), except for two BCL2-mcr primers; their position is indicated downstream of the first nucleotide of the AF275873 sequence. <b>B, C, and D.</b> Agarose gel electrophoresis of PCR products from different FCL patients and several positive control cell lines (DoHH2, K231, OZ, and SC1). Panel B and D contain the same samples and show complementarity in positivity, illustrating that tube C (mcr tube) has added value. The PCR products differ in size, related to different position of the <i>BCL2</i> breakpoints. The larger bands of lower density in the same lanes represent PCR products that extend to the next downstream germline JH gene segment or to the next upstream <i>BCL2</i> primer.

0062<figref idref="f0015"><b>Figure 12</b></figref><b>. Control gene PCR for assessment of amplifiability and integrity of DNA samples. A.</b> Schematic diagram of five control genes exons and the five primer sets for obtaining PCR products of 600 bp, 400 bp, 300 bp, 200 bp, and 100 bp. The relative position of the control gene primers is given according to their most 5' nucleotide downstream of the 5' splice site of the involved control gene exon. <b>B.</b> Control gene PCR products of six DNA samples, separated in a 6% polyacrylamide gel. Two control samples contained high molecular weight DNA (outer lanes) and four DNA samples were obtained from paraffin-embedded tissue samples, showing reduced amplifiability (e.g. GBS-4 50 ng versus GBS-4 500 ng) or reduced integrity of the DNA (PT-4).

0063<figref idref="f0016"><b>Figure 13</b></figref><b>. Multicolor GeneScanning for supporting the rapid and easy identification of TCR gene rearrangements. A.</b> Two-color analysis of <i>TCRB</i> tube A with differential labeling of Jβ1 primers (TET-labeled; green) and Jβ2 primers (FAM labeled; blue). The top panel nicely shows the two polyclonal Jβ1 and Jβ2 rearrangement patterns (c.f. <figref idref="f0010">Figure 7C</figref>), whereas the other two panels show clonal Jβ2 rearrangements. B. Two-color analysis of <i>TCRG</i> tube A with differential labeling of the Jγ1.3/2.3 primer (FAM-labeled; blue) and the Jγ1.1/2.1 (TET-labeled; green). The top panel nicely shows the polyclonal rearrangement patterns (c.f. <figref idref="f0011">Figure 8C</figref>), whereas the other two panels show clonal Jγ1.3/2.3 and clonal Jγ1.1/2. rearrangements, respectively. C. Three-color analysis of <i>TCRD</i> gene rearrangements with differential labeling of Jδ primers (FAM-labeled; blue), Dδ2 primer (HEX-labeled; green) and Dδ3 primer (NED-labeled; black). Within the complex rearrangement patterns of the <i>TCRD</i> tube (<figref idref="f0012">Figure 9C</figref>), the three-color analysis allows direct detection of Vδ-Jδ rearrangements (blue peaks), Dδ2-Jδ rearrangements (blue and green peaks, not fully comigrating because of differences in migration speed of the two fluochromosomes), Vδ2-Dδ3 rearrangement (black peaks), and Dδ2-Dδ3 rearrangement (comigrating green and black peaks).

MATERIALS AND METHODS

Selection of PCR targets: aiming for complementarity

0064It was decided to aim for the availability of at least one PCR-detectable clonality target in each lymphoid malignancy. In mature B-cell malignancies this aim might be hampered by the occurrence of somatic hypermutations in Ig genes, which are particularly found in follicular and post-follicular B-cell malignancies. Therefore it was decided to include PCR targets that have some degree of complementarity.

0065Several rationales were used for target selection: <ul id="ul0003" list-style="dash" compact="compact"><li><i>IGH</i> genes: not only complete V_H-J_H rearrangements but also incomplete D_H-J_H rearrangements were included as PCR targets, because D_H-J_H rearrangements are probably not affected by somatic hypermutations;</li><li><i>IGK</i> and <i>IGL</i> genes: both Ig light chain genes were included as PCR targets, because this increases the chance of finding a PCR-detectable Ig gene rearrangement in each mature B-cell malignancy;</li><li><i>IGK</i> genes: not only Vκ-Jκ: rearrangements were included, but also rearrangements of the kappa deleting element (Kde), because they occur on one or both alleles in (virtually) all Igλ⁺ B-cell malignancies and in one third of Igκ⁺ B-cell malignancies and because Kde rearrangements are probably not affected by somatic hypermutation;</li><li><i>TCRB</i> genes: both complete Vβ-Jβ and incomplete Dβ-Jβ rearrangements, because complete and incomplete <i>TRCB</i> gene rearrangements occur in all mature TCRαβ⁺ T-cell malignancies and also in many TCRγδ⁺ T-cell malignancies;</li><li><i>TCRG</i> genes: this classical PCR clonality target is useful in all T-cell malignancies of the TCRγδ and the TCRαβ lineage.</li><li><i>TCRD</i> genes: this is a potentially useful target in immature T-cell malignancies as well as in TCRγδ⁺T-cell malignancies;</li><li><i>TCRA</i> gene: this gene was not included as PCR target, because of its high degree of complexity with ∼50 V and 61 J gene segments. Furthermore, all T-cell malignancies with <i>TCRA</i> gene rearrangements contain <i>TCRB</i> gene rearrangements and generally also have <i>TCRG</i> gene rearrangements;</li><li>functional gene segments: most suspect lymphoproliferations concern mature lymphocytes, which consequently have functional Ig or TCR gene rearrangements. Therefore PCR primer design aimed at inclusion of (virtually) all functional Ig/TCR gene segments.</li><li>well-defined chromosome aberrations: t(11;14) with <i>BCL1-IGH</i> and t(14;18) with <i>BCL2-IGH</i> were included as additional targets, because these two aberrations are PCR-detectable at relatively high frequencies in lymphomas i.e. in 30% of mantle cell lymphoma (MCL) and in 60 to 70% of follicular cell lymphomas (FCL), respectively.</li></ul>

Primer design for multiplex PCR

0066Precise detection of all V, D, and J gene segments in rearranged Ig and TCR genes would require many different primers (Table 2). For some gene complexes this might be possible (e.g. <i>TCRG</i> and <i>TCRD</i>), but for other loci in practice this is impossible because of the high number of different gene segments. To solve this problem, family primers can be designed, which recognize most or all gene segments of a particular family (Table 2). Alternatively, consensus primers can be made, which recognize conserved sequences that occur in many or all involved gene segments.

0067The design of family primers and consensus primers balances between a limited number of primers and maximal homology with all relevant gene segments. In this study, we aimed at maximal homology with all relevant gene segments (particularly functional gene segments) in order to prevent suboptimal primer annealing, which might cause false-negative results. Furthermore, we aimed at the design of specific family primers without cross-annealing to other families

0068In order to limit the number of PCR tubes per locus, multiplexing of PCR primers became important for practical reasons. Consequently, special guidelines were developed to ensure maximal possibilities for designing primers useful in multiplex PCR tubes. For this purpose dr. W. Rychlick (Molecular Biology Insights, Cascade; CO, USA) provided his specially-adapted OLIGO 6.2 software program and supported the development of the guidelines for optimal primer design.

0069The general guidelines for primer design were as follows: <ul id="ul0004" list-style="dash" compact="compact"><li>the position of the primers should be chosen in such a way that the size of the PCR products would preferably be <300 bp (preferably 100 to 300 bp) in order to be able to use paraffin-embedded material;</li><li>a minimal distance to the junctional region of preferaby >10-15 bp should be taken into acount (in order to avoid false-negativity due to impossibility of the 3' end of the primer to anneal to the rearranged target because of nucleotide deletion from the germline sequence);</li><li>primers preferably should not be too long (e.g. <25 nucleotides).</li></ul>

0070The following parameters were used for primer design with the OLIGO 6.2 program: <ul id="ul0005" list-style="dash" compact="compact"><li>search for primers should be performed with <i>moderate</i> stringency;</li><li>primer efficiency (PE) value should preferably be ∼400 (and >630, if the primer is to be used as consensus primer for other gene segments as well);</li><li>the most stable 3' dimer of upper/upper, lower/lower, or upper/lower primers should not exceed -4 Kcal (moderate search strategy); the most stable dimer overall being less important;</li><li>in view of multiplex PCR, the following guidelines were taken into account: a common primer would have to be designed in the most consensus region (i.e. high PE in consensus search), whereas individual primers (family or member) have to be designed in the least consensus region (i.e. low PE value of that primer for gene segments that should not be covered) to avoid cross-annealing to other gene segments and thereby multiple (unwanted) PCR products.</li></ul>

PCR protocol

0071A standardised PCR protocol was developed based on pre-existing experience from earlier European collaborative studies. After initial testing and approval, the protocol was accepted as summarized in Table 3.

Techniques for analysis of PCR products obtained from Ig/ TCR gene rearrangements

0072The PCR products obtained from Ig and TCR gene rearrangements have to be analysed for discrimination between monoclonal lymphoid cells with identical junctional regions and polyclonal lymphoid cells with highly diverse junctional regions.

0073Based on the combined experience of the participating laboratories, two techniques were selected: heteroduplex (HD) analysis and Gene Scanning (GS) analysis. HD analysis uses double-stranded PCR products and takes advantage of the length and composition of the junctional regions, whereas in GS single-stranded PCR products are separated in a high resolution gel or polymer according to their length only (<figref idref="f0002">Figure 2</figref>).

Heteroduplex analysis of PCR products

0074PCR products obtained with <i>unlabeled</i> primers are denatured at high temperature (∼95°C for 5 min), followed by rapid random renaturation at low temperature (preferably at 4°C for 1 hour). This enforced duplex formation results in many different heteroduplexes with different migration speed in case of polyclonal lymphoproliferations, but resulting in homoduplexes with identical rapid migration in case of monoclonal lymphoproliferations. Electrophoresis of the homoduplexes in a 6% polyacrylamide gel results in a single band of predictable size, whereas the heteroduplexes form a smear at a higher position (<figref idref="f0002">Figure 2</figref>). The heteroduplex technique is rapid, simple and cheap (see Table 4 for technical details) and has a detection limit of ∼ 5 %. ^40.41 The detection limit is influenced by the frequency of polyclonal lymphocytes, because the formation of many heteroduplexes will also consume a part of the monoclonal PCR products.⁴¹

Genescanning analysis of PCR products

0075The PCR primers for GeneScanning analysis need to be labeled with a fluorochrome to allow detection of the PCR products with automated sequencing equipment (<figref idref="f0002">Figure 2</figref>).

0076The fluorochrome labeled single-strand (denatured) PCR products are size-separated in a denaturing polyacrylamide sequencing gel or capillary sequencing polymer and detected via automated scanning with a laser (see Table 5 for technical details). This results in a Gausian distribution of multiple peaks, representing many different PCR products in case of polyclonal lymphoproliferations, but gives a single peak consisting of one type of PCR product in case of a fully monoclonal lymphoproliferation (<figref idref="f0002">Figure 2</figref>).

0077GeneScanning is rapid and relatively simple, but needs expensive equipment. GeneScanning is generally more sensitive than heteroduplex analysis and can reach sensitivities of 0.5 to 1% of clonal lymphoid cells.

Control genes and paraffin-embedded tissues

0078In several European countries, fresh tissue material is not easily available for molecular diagnostics such as PCR-based clonality studies. Therefore one of the aims of the present study was to develop a strategy for PCR-based clonality studies in paraffin-embedded tissues.

0079To control for the quality and amplifiability of DNA from paraffin-embedded material, a special multiplex control gene PCR was developed, resulting in a ladder of five fragments (100 bp, 200 bp, 300 bp, 400 bp, and 600 bp). From 45 of the above described 90 cases sufficient paraffin-embedded tissue was available for DNA extraction. These DNA samples were tested in parallel to the freshly-obtained DNA samples, using the Control Gene multiplex tube as well as the Ig/TCR/BCLI/<i>BCL2</i> multiplex tubes for clonality diagnostics (see Example 10).

EXAMPLE 1. Complete <i>IGH</i> gene rearrangements: V_H-J_H

Background

0080The functional rearrangement of the <i>IGH</i> gene, first D_H to J_H and subsequently V to D_H-J_H, is followed by antibody expression, the hallmark of mature B-cells. The <i>IGH</i> gene is located on chromosome 14q32.3 in an area covering approximately 1250 kilobases. 46 to 52 functional VH segments (depending on the individual haplotype) have been identified, which can be grouped according to their homology in six or seven VH subgroups. In addition approximately 30 non-functional VH segments have been described. Furthermore, 27 DH segments and functional six JH segments have been consistently found (Table 2 and <figref idref="f0003">Figure 3A</figref>).⁵⁶

0081The VH segments contain three framework (FR) and two complementarity determining regions (CDR) (<figref idref="f0003">Figure 3B</figref>). The FRs are characterized by their similarity among the various VH segments whereas the CDRs are highly different even within the same V_H family. Furthermore, the CDRs represent the preferred target sequences for somatic hypermutations in the course of the germinal center reaction, which increase the variability within those regions. Although the FRs are usually less affected by somatic mutations, nucleotide substitutions may also occur within these regions, especially in B-cells under a heavy mutational process.

0082The highly variable V-D-JH regions can be amplified by PCR to detect clonal B-cell populations indicative of the presence of a malignant B-cell disorder. Clonal B-cells can be discriminated from polyclonal B-cells (i.e. normal or reactive lymphoid tissues) based on the identical size and composition of the clonal PCR products as compared to the many different polyclonal PCR products with a size range of approximately 60 bp, arranged in a Gaussian distribution. PCR-based strategies for detection of clonal B-cell populations in histological sections and cell suspensions have already been established in the early nineties. However, the initial PCR protocols used single VH consensus primers which were able to bind to one of the three framework regions, mainly FR3. Such consensus primers were not suitable to amplify all VH segments with the same efficiency leading to non-detectability of a significant number of clonal rearrangements. In addition, somatic mutations introduced in the course of the germinal center reaction are not restricted to the CDRs, but can also occur in FRs, thereby preventing primer annealing and consequently leading to absence of clonal PCR products despite the presence of a neoplastic B-cell population. This is especially true for follicular lymphomas, diffuse large B-cell lymphomas, and multiple myelomas which usually contain high numbers of somatic mutations.

0083To further increase the detection rate of the <i>IGH</i> PCR, several attempts have been made to design family-specific primers to overcome the limitations of consensus primers. However, these family-specific primers are largely based on the sequences of the previous consensus primers. Although these PCR strategies have helped to improve the detection rate, there is still a need of primer systems which are less sensitive to somatic hypermutations, thus allowing amplification of (virtually) all possible V-D-J_H rearrangements.

Primer design

0084According to the disclosed guidelines, three sets of V_H primers were designed with the help of the OLIGO-6.2 program corresponding to the three V_H frame work regions (FR1, FR2 and FR3) (<figref idref="f0003">Figure 3B</figref>). Each set of primers consisted of six or seven oligonucleotides capable to anneal to their corresponding V_H segments (V_H1 to VH₇) with no mismatches for most V_H segments and one or at most two mismatches for some rare V_H segments. The design was such that mismatches would be located at the very 5'-end of the primer. These V_H primer sets were used in conjunction with a single JH consensus primer, designed to anneal to the most homologous 3'-end of the six JH segments, approximately 35 bp downstream of the JH RSS. This ensures that all JH segments are detectable with the same binding efficiency and that the primer binding will not easily be affected by extensive nucleotide deletion in the course of the rearrangement process. In addition, there was no cross-annealing between the VH primers and the JH primer as evaluated by the OLIGO-6.2 program.

0085The JH primer was also designed to be used for amplification of other PCR targets, such as incomplete D_H-J_H rearrangements as well as t(11;14) (<i>BCL1-IGH</i>) and t(14;18) (<i>BCL2-IGH</i>). This allows the detection of different PCR products by GS analysis employing the same labeled J_H primer.

Results of initial testing phase

0086The initial testing of the newly designed V_H-J_H PCR was done by separate application of each V_H primer together with the JH primer in an individual PCR. For this purpose, DNA extracted from B-cell lines as well as well-defined clonal patient samples was used. Furthermore, clonal rearrangements were tested for sensitivity by serial dilution in DNA extracted from reactive tonsils. Clonal control samples were not available for each possible <i>IGH</i> rearrangement, but all major V_H segments and several rarely rearranged VH segments have been included in the initial testing phase.

0087All primer pairs worked with high efficiency and sensitivity. The expected clonal VH rearrangements were detectable and the sensitivity was at least 1% (10^-2). There was no background within the expected size range and the amplification of tonsillar DNA gave the expected Gaussian distribution curve. (<figref idref="f0004">Figure 3C</figref>, D, and E)

0088Based on these results we started the next phase of the initial primer testing by combining the VH primers into three sets, each specific for one of the three framework regions, which were used together with the common JH primer (<figref idref="f0003">Figure 3B</figref>). The results were the same as those obtained with single primer pairs, but with a slightly lower sensitivity. In addition, no nonspecific products were amplified within the expected size range, with the exception of a 340 bp PCR product which appeared in the FR1 multiplex PCR. This PCR product was generated irrespective of the source of the DNA (lymphoid and non-lynphoid) used for PCR, whereas no PCR product was obtained when no DNA template was applied. Furthermore, this amplicon was only detectable in heteroduplex analyis, not in GeneScanning. This indicates that the fluorescent labeled JH primer was not involved in the generation of this PCR product. Sequence analysis of this PCR product disclosed a VH4 fragment amplified by the FR1 VH4 primer in conjunction with the FR1 V_H2 primer which apparently acted as a downstream primer by binding to the intronic V_H4 sequence. This problem could be solved by designing a new FR1 VH2 primer which was located 25 bp upstream to the previous primer binding site.

Results of general testing phase

0089The approved <i>IGH</i> PCR was applied to the 90 Southern blot defined DNA samples, which were derived from well-characterized cases. Six of the 11 laboratories involved in the general testing phase performed GS analysis of the PCR products and five performed HD analysis. In addition several polyclonal as well as monoclonal samples (cell line DNA) were included as controls. 45 of these cases displayed dominant PCR products after GS analysis and 40 cases after HD detection, indicating the presence of a monoclonal B-cell population. The clonal rearrangements were detectable with all three FR primer sets in 33 of the 45 clonal cases (GS) and in the remaining 12 with one or two of the three FR primer sets. It was concluded that most negative results were caused by somatic hypermutations in the primer binding site, preventing primer annealing and thus amplification.

0090The comparison of the V_H-J_H PCR results with the Southern blot results revealed a high degree of concordance. 85% (46 out of 55) and 76% (42 out of 55) of the samples with rearranged V_H genes by Southern blot analysis showed a dominant amplification product by GS analysis and HD analysis, respectively. Vice versa, all but two samples harboring germline V_H genes by Southern blot displayed a polyclonal pattern by GS and HD analysis.

Conclusion

0091In conclusion, the three multiplex PCRs for detection of clonal V_H-J_H rearrangements provide a new and reliable assay to identify clonal B-cell proliferations. The combined use of standardized primers in the three different FRs helps to decrease the rate of false-negative results due to somatic hypermutation in primer binding sites of the involved V_H gene segments. <b>EXAMPLE 2. Incomplete <i>IGH</i> gene rearrangements: D_H-J_H</b>

Background

0092The formation of complete V-D-J rearrangements in the <i>IGH</i> locus one chromosome 14q32.3 is a sequential process that occurs in two steps: V_H coupling is generally preceded by an initial rearrangement between D_H and J_H gene segments in early precursor-B cells (reviewed by ⁵⁷). In addition to the many distinct V_H gene segments and the six functional J_H gene segments (see Example 1), the human <i>IGH</i> locus also contains 27 D_H gene segments.⁵⁸ Based on sequence homology, the 27 D_H segments can be grouped into seven families: D_H1 (formerly known as DM), D_H2 (DLR), D_H3 (DXP), D_H4 (DA), D_H5 (DK), D_H6 (DN), and D_H7 (DQ52); all families comprise at least four members, except for the seventh which consists of the single D_H7-27 segment just upstream of the J_H region (<figref idref="f0003">Figure 3A</figref>).^58.59

0093Recombination between any of the D_H and J_H segments will result in the formation of incomplete D_H-J_H joints, which can easily be detected in bone marrow-derived CD10⁺ / CD19- precursor B-cells ^60.61 and hence also in a subset (20-25 %) of precursor B-cell acute lymphoblastic leukemias, which show an immature genotype.⁶² Sequencing revealed a predominance of D_H2 (D_H2-2), D_H3 (D_H3-9) , and D_H7-27 gene segments in precursor B-ALL, comprising 36%, 33%, and 19% of all identified segments, respectively.⁶²

0094However, also in mature B-cell malignancies incomplete D_H-J_H rearrangements have been reported.^61.63 Moreover, even in a subset of IgH-negative multiple myelomas, which can be considered as the most mature type of B-lineage malignancy, D_H-J_H joints were observed.⁶⁴ These D_H-J_H rearrangements were derived from the non-coding second allele and involved segments from D_H1 to D_H4 families.⁶⁴ Based on the description of D_H-J_H joints in precursor-B-ALL and multiple myelomas, it is assumed that incomplete D_H-J_H rearrangements are also present in other types of B-cell leukemias and lymphomas. In immature T-cell malignancies D_H-J_H couplings have been identified as cross-lineage rearrangements;³⁴ interestingly, these almost exclusively occurred in the more immature non-TCRaαβ⁺ T-ALL subset and mainly involved the more downstream D_H6-19 and D_H7-27 segments. The latter segment is frequently (up to 40%) used in fetal B cells but rarely in adult B cells.^65.66 Human adult precursor and mature B cells mainly seem to use D_H2 and D_H3 family segments, as evidenced from sequences of complete VH-D_H-J_H rearrangements.⁶⁶

0095Although the exact frequencies of incomplete D_H-J_H couplings in different types of mature B-cell malignancies are largely unknown, it is clear that they will at least be lower than those of V_H-J_H joinings. Nevertheless, D_H-J_H rearrangements might still represent an important complementary target for PCR-based clonality assessment. This presumed contribution of D_H-J_H rearrangements as PCR target is based on the assumption that incomplete rearrangements in the <i>IGH</i> locus will not to contain somatic hypermutations, because transcription starting from the promoters in the V gene segments does not occur, which is regarded as an essential prerequisite for somatic hypermutation to take place.^67,68 Especially in those types of B-lineage proliferations in which somatic hypermutations are frequent, PCR analysis of a possible D_H-J_H recombination product might therefore be relevant, and sometimes even the only possibility to detect the B-cell clone.

Primer design

0096Based on the high degree of homology within each D_H family, seven family-specific D_H primers were designed (<figref idref="f0005">Figure 4</figref>) in combination with the consensus J_H primer that is also used for detection of V_H-J_H rearrangements (see Example 1) and t(11;14) (<i>BCL1-IGH</i>) and t(14;18) (<i>BCL2-IGH</i>) (Examples 8 and 9). Primers were designed such that cross-annealing to other DH family segments would be minimal or preferably absent, resulting in distinct positions for the various family primers relative to the RSS elements (<figref idref="f0005">Figure 4</figref>). The expected PCR product sizes of D_H-J_H joints range from 110-130 bp (for D_H7-J_H joinings) to 395-415 bp (for D_H3-J_H rearrangements). Of note, due to the position of the D_H7-27 segment close to the segments in the J_H region, PCR products of 211 bp (and also 419,1031,1404,1804, and 2420 bp in case of primer annealing to downstream J_H gene segments) will be amplified from non-rearranged alleles and will be detected as a ladder of germline bands in virtually every sample.

Results of initial testing phase

0097For initial testing of the individual D_H primers, high tumor load precursor B-ALL or T-ALL samples with well-defined clonal D_H-J_H rearrangements were used. Under standard PCR conditions using 1.5 mM MgCl₂ and Ampli<i>Taq</i> Gold buffer, all seven primer combinations appeared to detect the clonal D_H-J_H targets with product lengths within the expected size ranges. Cross-annealing of the D_H primers to rearranged gene segments from other D_H families was only very weak or not observed at all. Furthermore, also in healthy control tonsillar or MNC DNA PCR products of the correct size ranges were observed. Nonspecific annealing of the primers was not observed for virtually all primers sets, using non-template specific control DNA; only in case of the D_H2 / J_H primer set a (sometimes faint) 340-350 bp product was observed in HeLa DNA. Further sequencing revealed that this nonspecific product was due to false priming of the D_H2 primer to a DNA sequence upstream of the JH4 segment. However, as the size of this nonspecific product was so different from the sizes of any of the true D_H-J_H PCR products, it was decided not to design a new D_H2 primer. In fact, the nonspecific 350 bp band can be employed as an internal marker for successful DNA amplification and hence the quality of the template DNA, being hardly or only faintly visible when enough clonal or polyclonal D_H-J_H template is available (e.g. in tonsillar DNA or DNA from particular leukemic samples), but being especially strong in samples containing low numbers of lymphoid cells with D_H-J_H rearrangements.

0098Serial dilutions of DNA from the clonal reference samples into tonsillar DNA generally resulted in sensitivities of 5% or lower (0.5-1% in case of the D_H6-J_H rearrangement) using HD analysis; sensitivities in GS analysis were generally 1-2 dilution steps better, i.e. 1% or lower. The clonal D_H7-J_H target could only be detected with a sensitivity of ∼10%, which is most probably caused by primer consumption in PCR amplicons involving the non-rearranged germline D_H7 and J_H gene segments.

0099Although the initial multiplex strategy, as suggested from the OLIGO 6.2-assisted primer design, was to divide the various DH primers over two tubes, it was decided after testing various multiplex approaches to combine all primers into one multiplex tube (tube D of <i>IGH</i> clonality assay), except for the DH7 primer, which was included in a separate tube (tube E of <i>IGH</i> clonality assay). The reason to exclude the DH7 primer was the complicated germline pattern, due to easy amplification of alleles with non-rearranged DH7 segments. Using this two-tube multiplex approach, all clonal reference samples were still detectable. Under multiplex conditions the detection limits for these various clonal targets were logically less optimal as compared to the single assays, ranging from ∼5% (DH3, DH4, and DH6) to ∼10% (DH2, and DH5). For the DH1 clonal reference sample that was available, a sensitivity of ∼20% was observed; at a later stage the DH1-JH rearrangement of cell line KCA was found to be detectable down to 10% in the multiplex assay. As tube E only contains the DH7 primer, the 10% sensitivity for this tube was the same as mentioned before. The same multiplex analysis performed with 500 ng instead of 100 ng DNA of the serial dilutions, resulted in slightly better sensitivities. The use of serial dilutions in MNC DNA instead of tonsillar DNA did not clearly affect detection limits of the assays for DH-JH recombinations.

Results of general testing phase

0100Following initial testing in the three laboratories involved in primer design, the developed <i>IGH</i> DH-JH multiplex PCR assay was further evaluated using the 90 Southern blot-defined samples. Every sample was analyzed in parallel in four laboratories by HD analysis and in five laboratories by GS analysis; in another two laboratories all samples were analyzed by both techniques. All together a total of six HD and seven GS analysis results were obtained per sample per tube. Despite concordant results (> 80% of laboratories with identical results) in the vast majority of samples, nine showed inter-laboratory discordancies in tube D. Further analysis revealed that these could be explained by either the presence of a small clone with weak clonal products, or to large size products (∼390 and larger). In a few cases the products were so large, that only after sequencing it became clear that they concerned true but extended DH-JH rearrangements, either from upstream DH (e.g. DH6-25-DH1-26-JH in NL-12) or from downstream JH gene segments (e.g. DH6-25-JH4-JH5 in PT-14). In all three cases (NL-17, mycosis fungoides; FR-1, B-CLL; FR-5, FCL) in which clonal products were found using tube E, the results were completely concordant between laboratories.

0101When evaluating results from HD and GS analysis, it appeared that these were comparable, although in general the number of laboratories showing identical results was slightly higher upon HD as compared to GS analysis (<figref idref="f0005">Figure 4B and C</figref>).

0102Direct comparison of DH-JH multiplex PCR results with SB data is virtually impossible, as hybridization with a single probe (IGHJ6) in the JH region does not allow discrimination between VH-JH and DH-JH rearrangements. In three samples it was clear that detection of clonal products of the combined VH-JH and DH-JH assays did not fit with configuration of the <i>IGH</i> locus in SB analysis. Remarkably, no clonal DH-JH PCR products were observed in the pre-follicular B-cell malignancies. In contrast, 11/16 B-CLL samples and 12/25 (post-)follicular B-cell malignancy samples did contain clonally rearranged DH-JH PCR products. In three of the eighteen T-cell malignancy cases clonal DH-JH rearrangements were seen; these concerned T-LBL (ES-9) and mycosis fungoides (NL-17) cases with SB-detected <i>IGH</i> rearrangements, and a case of T-NHL/EATL (PT-4) without SB-detected <i>IGH</i> rearrangements, probably because of the low tumor load of &lt;15%. All 15 reactive cases only showed polyclonal DH-JH PCR products, in accordance with SB results. In category D with difficult diagnoses, three samples (PT-12, GBS-10, and GBN-8) showed clonal <i>IGH</i> DH-JH PCR products, which was in line with SB data as well as <i>IGK</i> PCR data in two of three cases; in another two samples (PT-6 and GBS-9), both T-cell rich B-NHL cases, clonal DH-JH products were found in addition to clonal <i>IGK</i> and/or <i>IGL</i> products, but without evidence for clonality from SB analysis, which might best be explained by the small size of the B-cell clone in these samples.

0103In order to determine the additional value of DH-JH PCR analysis, the results were compared to those of VH-JH PCR analysis. In five (NL-4, PT-14, GBN-2, FR-7, NL-12) B-cell malignancies clonal DH-JH PCR products were found, whereas only polyclonal V_H-J_H PCR products were observed.

Conclusion

0104In conclusion, based on the initial and general testing phases, DH-JH PCR analysis appears to be of added value for clonality assessment. Although HD analysis results might be interpreted slightly more easily, there is no clear preference for either HD or GS analysis as they are both suitable for analyzing amplified PCR products. A potential difficulty in DH-JH PCR analysis is the relatively large size range of expected PCR products, due to scattered primer positions and to extended amplifications from upstream DH or downstream JH gene segments, implying that long runs are recommended for GS analysis. Finally, the remarkable position of the DH7-27 gene segment in the <i>IGH</i> locus causes a ladder of germline amplification products in tube E, with clonal products being easily recognizable as much smaller bands / peaks.

EXAMPLE 3. <i>IGK</i> gene rearrangements: Vκ-Jκ, Vκ-Kde / intronRSS-Kde

Background

0105The human <i>IGK</i> light chain locus (on chromosome 2p11.2) contains many distinct Vκ gene segments, grouped into seven Vκ gene families, as well as five Jκ gene segments upstream of the Cκ region.Originally, the Vκ gene segments were designated according to the nomenclature as described by Zachau et al.⁶⁹ An alternative nomenclature groups the Vκ gene segments in seven families and is used in the ImMunoGeneTics database. ⁴⁶ Here we follow the latter nomenclature. The Vκ1, Vκ2, and Vκ3 families are multimember families including both functional and pseudo gene segments, whereas the other families only contain a single (Vκ4, Vκ5, Vκ7) or a few segments (Vκ6).⁷⁰ Remarkably, all Vκ gene segments are dispersed over two large duplicated clusters, one immediately upstream and in the same orientation as the Jκ segments, and the other more distal and in an inverted orientation (<figref idref="f0006">Figure 5A</figref>).⁷¹ The latter implies that so-called inversion rearrangements are required to form Vκ-Jκ joints involving Vκ genes of the distal cluster. In addition to the Vκ and Jκ segments, there are other elements in the <i>IGK</i> locus that can be involved in recombination. The kappa deleting element (Kde), approximately 24 kb downstream of the Jκ-Cκ region, can rearrange to Vκ gene segments (Vκ-Kde), but also to an isolated RSS in the Jκ-Cκ intron (intronRSS-Kde).^{24, 72} Both types of rearrangements lead to functional inactivation of the <i>IGK</i> allele, through deletion of either the Cκ exon (intronRSS-Kde rearrangement) or the entire Jκ-Cκ area (Vκ-Kde rearrangement).

0106As human <i>IGK</i> recombination starts in precursor B-cells in the bone marrow, <i>IGK</i> rearrangements can also be detected in precursor B-cell acute leukemias (30-45% of alleles, depending on age). Although Vκ-Jκ joinings are present, these <i>IGK</i> rearrangements mainly concern recombinations involving Kde (25-35% of alleles). In childhood precursor B-ALL Vκ-Kde recombination predominates over intron-Kde, whereas in adult ALL the deletions exclusively concern Vκ-Kde couplings.^{20, 73, 74} In chronic B-cell leukemias <i>IGK</i> rearrangements are even more frequent, being detectable on 75% (Igκ⁺ cases) or even 95% (Igλ⁺ cases) of all <i>IGK</i> alleles. By definition, functional Vκ-Jκ rearrangements are found on at least one allele in Igκ⁺ B-cell leukemias; the non-coding second allele is either in germline configuration, or inactivated through Vκ-Kde (8% of alleles) or intronRSS-Kde (8% of alleles) recombination. Kde rearrangements are frequent in Igλ⁺ B-cell leukemias (∼85% of alleles), with a slight predominance of intronRSS-Kde recombinations over Vκ-Kde rearrangements. This implies that virtually all Igλ⁺ leukemias contain a Kde rearrangement, while potentially functional Vκ-Jκ couplings are relatively rare.^{24, 75} Several studies have shown that Vκ gene segment usage is almost identical between various normal and malignant B-cell populations and largely reflects the number of available gene segments within each family. Both in Vκ-Jκ as well as in Vκ-Kde rearrangements, Vκ gene segments from the first four families (Vκ1 to Vκ4) predominate. Vκ2 gene usage appeared to be higher in precursor B-ALL than in more mature B-cell lymphoproliferations or normal B cells. Remarkably, the distal inverted Vκ cluster was rarely used in Vκ-Jκ rearrangements, whereas Vκ pseudogene segments were never involved, also not in Igλ⁺ cases.⁷⁶ Little is known about Jκ gene segment usage, but sparse data show that Jκ1, Jκ2, and Jκ4 are the most frequently used Jκ gene segments.⁷⁵

0107Vκ-Jκ rearrangements can be important complementary PCR target for those types of B-cell proliferations in which somatic hypermutations may hamper amplification of the VH-JH target, but recombinations involving Kde are probably even more valuable. Deletion of intervening sequences in the Jκ-Cκ intron results in the removal of the <i>IGK</i> enhancer, which is thought to be essential for the somatic hypermutation process to occur. Rearrangements involving Kde are therefore assumed to be free of somatic hypermutations, and hence should be amplified rather easily.

Primer design

0108Using OLIGO 6.2 software, six family-specific Vκ primers were designed to recognize the various Vκ gene segments of the seven Vκ families; the Vκ6 family gene segments were covered by the Vκ1 family primer (<figref idref="f0006">Figure 5B</figref>). In case of the relatively large Vκ1, Vκ2, and Vκ3 families only the functional Vκ gene segments were taken into consideration, as the less homologous pseudo gene segments complicated optimal primer design too much. The family-specific Vκ primers were designed to be used in combination with either a set of two Jκ primers (Jκ1-4, covering the first four Jκ segments and Jκ5 covering the fifth) or a Kde primer (<figref idref="f0006">Figure 5B</figref>). For analysis of Kde rearrangements an additional forward primer recognizing a sequence upstream of the intronRSS was made. In order to show minimal cross-annealing to other Vκ family segments and still be useful in multiplex reactions, the various primers could not be designed at similar positions relative to RSS elements (<figref idref="f0006">Figure 5B</figref>). The expected PCR product sizes of Vκ-Jκ joints range from ∼115-135 bp (for Vκ7-Jκ joints) to ∼280-300 bp (Vκ2-Jκ rearrangements). For the Kde rearrangements, product size ranges are from ∼195-215 bp (Vκ7-Kde) to ∼360-380 bp (Vκ2-Kde), whereas the intronRSS-Kde products are ∼275-295 bp.

Results of initial testing phase

0109For initial testing of the individual primers, several cell lines and patient samples with precisely defined clonal Vκ-Jκ, or Vκ-Kde / intronRSS-Kde rearrangements were used. The patient samples with Vκ-Jκ joints mostly concerned chronic B-cell leukemias, which were additionally selected on basis of a high tumor load for easy and sensitive detection of the involved rearrangement. Unfortunately, clonal reference samples were not available for all Vκ-Jκ targets; especially the more rare types of rearrangements involving Vκ5, Vκ7 and/or Jκ5 were not represented in the series of reference samples. For these targets and also for the targets for which clonal reference samples were available, healthy control tonsillar or MNC DNA samples were employed, in which PCR products of the correct expected sizes were indeed observed. The only exception was the Vκ7 / Jκ5 primer combination; most probably Vκ7-Jκ5 joinings are so rare in normal B cells, that these PCR products were hardly or not detectable in tonsils. Rearranged products within the expected size ranges could be detected in all clonal reference samples, under standard PCR conditions using 1.5 mM MgCl₂ and either ABI Gold Buffer or ABI Buffer II. However, in a few cases weak amplification of particular Vκ-Jκ rearrangements was observed with other Vκ family / Jκ primer sets, due to slight cross-annealing of the Vκ3 primer to a few Vκ1 gene segments. Furthermore, in a few of the clonal reference samples clear additional clonal PCR products were seen with other Vκ /Jκ or even Vκ /Kde and intronRSS / Kde primer sets; in most samples this could be explained by the complete configuration of the two <i>IGK</i> alleles. This occurrence of multiple clonal PCR products illustrates the complexity of <i>IGK</i> rearrangement patterns in a given cell sample, mainly caused by the potential occurrence of two clonal rearrangements on one allele (Vκ-Jκ and intron RSS-Kde). This complexity does not hamper but support the discrimination between polyclonality and monoclonality.

0110No nonspecific annealing of the primers was observed for any of the Vκ-Jκ and Vκ-Kde / intron RSS-Kde primer sets, when using HeLa DNA as a non-template specific control. Serial dilutions of DNA from the clonal reference samples into tonsillar DNA generally resulted in sensitivities of 5-10 % for Vκ-Jκ rearrangements and 1-10 % for Vκ-Kde rearrangements, using HD analysis. In general, the sensitivities in GS analysis were approximately one dilution step better. The only slightly problematic target was the intronRSS-Kde target that could only be detected down to the 10% serial dilution in the employed patient sample. This is probably caused by the fact that intronRSS-Kde rearrangements are abundant in DNA from both Igκ⁺ and Igλ⁺ tonsillar B cells, which were used in the dilution experiments.

0111The multiplex strategy that was chosen after testing several approaches consisted of two different multiplex PCR reaction tubes. In the Vκ-Jκ tube (tube A) all Vκ primers were combined with both Jκ primers, whereas tube B contained all Vκ primers plus the intronRSS primer in combination with the Kde reverse primer (<figref idref="f0006">Figure 5B</figref>). All beforementioned clonal reference samples were detectable using this two-tube multiplex approach. Of note is the observation that in non-clonal tonsil samples a predominant, seemingly clonal band of ∼150 bp was detected using the Vκ-Jκ multiplex tube A analysis. The presence of this product, which is seen in HD analysis but especially in GS analysis, can be explained by the limited heterogeneity of Vκ-Jκ junctional regions leading to a high frequency of products of an average size of ∼150 bp. Furthermore, in some samples a sometimes weak 404 bp nonspecific band was observed in tube B. Although sensitivities were on average slightly better in other multiplex approaches in which the Vκ primers were further subdivided over multiple tubes, the feasibility of having only two tubes to analyze all relevant <i>IGK</i> rearrangements, finally was the most important argument for choosing the two-tube multiplex strategy as given in <figref idref="f0006">Figure 5B</figref>. Detection limits for the various clonal targets in the two-tube multiplex approach were ∼10% for most of the clonal Vκ-Jκ rearrangements (Vκ1-Jκ4, Vκ2-Jκ4, Vκ3-Jκ4) derived from informative samples with a high tumor load; several of the Vκ-Kde targets were detectable with a still reasonable sensitivity of ∼10%, but a few other samples containing Vκ2-Kde, Vκ5-Kde, and also intronRSS-Kde targets showed detection limits above 10%. Even the use of 500 ng serially diluted DNA instead of 100 ng hardly resulted in better sensitivities, whereas serial dilutions in MNC DNA did not affect the detection limits either. Nevertheless, detection limits of serial dilutions of reference DNA in water were all in the order of 0.5-1 %, which shows that the chosen multiplex <i>IGK</i> PCR assay as such is good. It is important to note that potential clonal cell populations in lymph nodes or peripheral blood in practice will have to be detected within a background of polyclonal cells, which can hamper sensitive clonality detection, especially in samples with a relatively high background of polyclonal B-cells.

Results of general testing phase

0112Following initial testing in the four laboratories involved in primer design, the developed <i>IGK</i> multiplex PCR assay was further evaluated using 90 Southern blot-defined samples. Every sample was analyzed in parallel via HD (five laboratories) and GS (two laboratories) analysis; in another four laboratories all samples were analyzed by both techniques. Taken together, eight HD and five GS analysis results were available per sample per tube. In the vast majority of samples >80% of laboratories produced identical results, i.e. either clonal bands / peaks or polyclonal smears / curves in one or both tubes. However, in nine (∼10%) samples discordancies were found between laboratories, which remained after repetitive analysis of these samples. More detailed analysis revealed that in at least six cases the approximately 150 and 200 bp sizes of the clonal products in tube A could not easily be discriminated from polyclonal products of roughly the same size. This is an inherent difficulty in especially Vκ-Jκ analysis, which is caused by the relatively limited junctional heterogeneity of these rearrangements. In two samples the results from tube B were however so clear in all laboratories with both techniques that in fact no discrepancy prevailed. In one sample (ES-8) a large product of around 500 bp appeared to be the reason for discrepant inter-laboratory results; further sequencing revealed that amplification starting from the downstream Jκ segment caused production of an extended Vκ1-Jκ3-Jκ4 PCR product.

0113When evaluating results from HD and GS analysis, it appeared that these were rather comparable, although in general the number of laboratories showing identical results was slightly higher upon HD as compared to GS analysis (<figref idref="f0007">Figure 5C and D</figref>). Remarkably, in one sample (GBS-4) HD analysis revealed a clear product in both tubes, whereas GS analysis only showed polyclonality. Cloning of the HD product showed a peculiar Vκ3-Vκ5 PCR product, which was not observed in any other sample; the Vκ-Vκ configuration of this product explained why it was not detected with labeled Jκ primers in GS analysis.

0114Comparison of PCR results with SB data revealed no SB-PCR discrepancies in the pre-follicular B-cell malignancies and B-CLL samples; in line with the presence of rearranged <i>IGK</i> bands in SB analysis, all samples contained clonal <i>IGK</i> PCR products. In contrast, in the 25 (post-)follicular B-cell malignancy samples clonal <i>IGK</i> PCR products were missed in four DLCL cases (ES-5, PT-13, PT-14, FR-7) and one PC leukemia (NL-19) with both techniques and in another DLCL case (GBS-4, see above) with GS analysis only. In all cases this was most probably caused by somatic hypermutation. Interestingly, in one FCL case (NL-4), a clonal PCR product was found, whereas SB analysis revealed a germline band in case of the <i>IGK</i> genes and weak clonal bands upon <i>IGH</i> analysis. In all 18 T-cell malignancy cases and all 15 reactive cases (category C) polyclonal <i>IGK</i> PCR products were found in accordance with SB results, except for one peripheral T-NHL case (FR-10). Next to the clonal TCR and <i>IGK</i> products this sample also showed clonal <i>IGH</i> and <i>IGL</i> PCR products, but no clonal Ig rearrangements in SB analysis, probably reflecting the presence of a small additional B-cell clone in this sample. Finally, in the category with difficult diagnoses (D), two samples (GBS-10 and GBN-8) showed clonal <i>IGK</i> PCR products, in line with SB data; however, in another two samples (PT-6 and GBS-9), both T-cell rich B-NHL cases, clonal <i>IGK</i> PCR products were found as well as clonal <i>IGH</i> and/or <i>IGL</i> products, but without evidence for clonality from SB analysis. Also this discrepancy can probably be explained by the small size of the B-cell clone in these two patient samples.

0115To determine the additional value of analyzing the <i>IGK</i> locus, we compared the results of <i>IGK</i> PCR analysis to those of <i>IGH</i> PCR analysis. In five (ES-2, NL-4, PT-8, GBN-2, ES-8) of the nine samples in which no clonal VH-JH PCR products were found, clonal products were readily observed in <i>IGK</i> analysis. When taking into account both VH-JH and DH-JH analysis, <i>IGK</i> PCR analysis was still complementary to <i>IGH</i> PCR analysis in three of these cases in detecting clonal Ig PCR products.

Conclusion

0116In conclusion, based on the initial and general testing phases as well as preliminary evidence from use of these multiplex assays in pathologically well-defined series of lymphoproliferations, PCR analysis of the <i>IGK</i> locus has clear (additional) value for clonality detection. Nevertheless, care should be taken with interpretation of seemingly clonal bands in especially tube A, due to the inherent restricted <i>IGK</i> junctional heterogeneity. As this problem is especially apparent in GS analysis, HD analysis is slightly preferred over GS analysis, although it should be marked that in some cases GS analysis may facilitate proper interpretation of results. Another potential pitfall is the relatively large size range of expected rearranged <i>IGK</i> products, due to scattered primer positions, and to extended amplifications from downstream Jκ gene segments. This implies that long runs are recommended for GS analysis. Finally, the inherent complexity of multiple rearrangements in the <i>IGK</i> locus (Vκ-Jκ and Kde rearrangements on the same allele), together with a low level of cross-annealing of Vκ primers, may occasionally result in patterns with multiple bands or peaks, resembling oligoclonality. However, with these considerations in mind, the two-tube <i>IGK</i> multiplex PCR system can be valuable in PCR-based clonality diagnostics.

EXAMPLE 4. <i>IGL</i> gene rearrangements

Background

0117<i>IGL</i> gene rearrangements are present in 5 to 10% of Igκ⁺ B-cell malignancies and in all Igλ⁺ B-cell malignancies. ⁷⁵ Therefore Vλ-Jλ rearrangements potentially represent an attractive extra PCR target for clonality studies to compensate for false-negative <i>IGH</i> VH-JH PCR results, mainly caused by somatic mutations. The <i>IGL</i> locus spans 1Mb on chromosome 22q11.2.^77-79 There are 73-74 Vλ genes over 900 kb, among which 30-33 are functional (<figref idref="f0008">Figure 6A</figref>). Upon sequence homology, the Vλ genes can be grouped in 11 families and three clans. Members of the same family tend to be clustered on the chromosome. The Jλ and Cλ genes are organized in tandem with a Jλ segment preceding a Cλ gene. Typically there are 7 J-Cλ gene segments, of which J-Cλ1, J-Cλ2, J-Cλ3, and J-Cλ7 are functional and encode the four Igλ isotypes (<figref idref="f0008">Figure 6A</figref>).^{80, 81} There is however a polymorphic variation in the number of J-Cλ gene segments, since some individual may carry up to 11 of them, due to an amplification of the Cλ2-Cλ3 region.^{82 83}

0118Several studies have shown that the <i>IGL</i> gene repertoire of both normal and malignant B cells is biased.^{46, 49, 64, 65} Thus over 90% of Vλ genes used by normal B cells belong to the Vλ1, Vλ2 and Vλ3 families, which comprise 60% of the functional genes. Moreover, three genes (2-14, 1-40, 2-8) account for about half of the expressed repertoire. While normal B cells use J-Cλ1, J-Cλ2 and J-Cλ3 gene segments in roughly equivalent proportions, neoplastic B cells tend to use predominantly J-Cλ2 and J-Cλ3 gene segments.⁴⁹ In both normal and malignant B cells the J-Cλ7 is used very rarely (1%). This latter finding was however challenged by a single-cell study of normal cells which found that more than half of the rearrangements employed the J-Cλ7 gene segments.⁸⁰ In contrast to the mouse, there is some junctional diversity due to exonuclease activity and N nucleotide addition in human <i>IGL</i> gene rearrangements.^{82, 85-87} It is however much less extensive than that of the <i>IGH</i> locus, and a number of rearrangements result from the directly coupling of germline Vλ and Jλ gene segments. Nevertheless, the <i>IGL</i> locus might represent an alternative complementary locus to <i>IGH</i> for B-cell clonality studies.

Primer design

0119Considering the biased Vλ repertoire, we chose to amplify only rearrangements which used the Vλ1, Vλ2 and Vλ3 gene segments. A single consensus primer recognizing both Vλ1 and Vλ2 gene segments, as well as a Vλ3 primer, were designed in regions of high homology between members of the same family (<figref idref="f0008">Figure 6B</figref>). Initial experiments showed that they worked as well in multiplex as separately. In fact, cross annealing of Vλ3 primer hybridizing to some Vλ1 or Vλ2 genes (or vice versa) could be observed when Vλ primers were used separately; it was not seen however in multiplex PCR.

0120A single consensus primer was designed for the Jλ1, Jλ2 and Jλ3 gene segments and has one mismatch in its central portion compared to each of the germline sequences. In preliminary experiments it was found to give rather better results than a combination of perfectly matched Jλ1 and Jλ2-Jλ3 primers. Since a single study reported the frequent usage of the Jλ7 gene in normal B cells,⁸⁸ we also designed a Jλ7 specific primer. When tested on various polyclonal B cell samples, we could hardly detect any signal in HD analysis, in contrast to amplifications performed on the same samples using the Jλ1, Jλ2-Jλ3 or the Jλ consensus primers. Similarly, we could not detect any rearrangement with this primer when analyzing a collection of monoclonal B-cell tumors. Based on these results as well as the other reports in the literature ⁴⁹, we concluded that the non-confirmed high frequency of Jλ7 rearrangements (in a single study) ⁸⁶had been caused by a technical pitfall and consequently, we decided not to include the Jλ7 primer. The PCR assay for the detection of <i>IGL</i> gene rearrangements in clonality study therefore consists of a single tube containing three primers (<figref idref="f0008">Figure 6B</figref>). This single tube was expected to detect the vast majority of the rearrangements.

Results of initial testing phase

0121Initial testing on a set of monoclonal and polyclonal samples showed they could very well be differentiated upon HD analysis of PCR products on 10% polyacrylamide gel electrophoresis (<figref idref="f0008">Figure 6C</figref>). Clonal <i>IGL</i> rearrangements were seen in the homoduplex region, with one or sometimes two weaker bands in the heteroduplex region, while polyclonal rearrangements appeared as a smear in the heteroduplex region (<figref idref="f0008">Figure 6C</figref>). Nonspecific bands were not observed. It should be noted that because of the limited size of the junctional region, it is extremely difficult to distinguish polyclonal from monoclonal rearrangements by running a simple polyacrylamide gel without performing a heteroduplex formation. Along this line, analysis of PCR products by GS proved to be less straightforward (<figref idref="f0008">Figure 6C</figref>). While monoclonal rearrangements were clearly identified, the polyclonal rearrangement pattern had an oligoclonal aspect due to the limited junctional diversity. The interpretation was more difficult, particularly to distinguish polyclonal cases from those with a minor clonal B-cell population in a background of polyclonal B-cells. We therefore recommend HD analysis as the method of choice to analyze <i>IGL</i> gene rearrangements.

0122The sensitivity of the assay, performed on several cases, proved to be about 5% (2.5% - 10%) when dilution of tumor DNA was done in PB-MNC and about 10% (5% - 20%) when diluted in lymph node DNA.

Results of general testing phase

0123The single-tube <i>IGL</i> PCR assay was evaluated on the series of 90 Southern blot defined lymphoid proliferations. This testing was done by nine laboratories, four with HD analysis only, one with GS analysis only, and four using both techniques. Clonal <i>IGL</i> gene rearrangements were detected in 19 cases. In 15 of them more than 70% concordance was obtained within the nine laboratories. In four cases less than 70% concordancy was obtained, which could be explained by minor clonal <i>IGL</i> gene rearrangements in three of them (ES-12, GB-10, and FR-10). This discordancy in the fourth case (PT-11) remains unexplained, particularly because no <i>IGL</i> gene rearrangements were detected by Southern blotting. As concluded from the initial testing, interpretation of GS analysis was more difficult than HD analysis, especially in the case of minor clonal populations. Of these 19 clonal <i>IGL</i> gene cases, 17 were B-cell proliferations (16 mature and one precursor B-cell). One case (ES12) corresponded to Hodgkin's disease and another (FR-10) to a T-NHL. Both had only a minor clonal <i>IGL</i> gene rearrangement, and FR-10 also displayed a clonal <i>IGK</i> gene rearrangement.

0124Comparison with Southern blot data showed some discrepancies. Six cases with clonal <i>IGL</i> gene rearrangements by PCR appeared as polyclonal by Southern blot analysis. Three of them (PT-6, ES-12, FR-10) concerned minor clonal populations which may have been below the sensitivity level of the Southern blot technique. In the three other cases (NL-19, ES-1, PT-11) a clonally rearranged band may have been missed by the fairly complex rearrangement pattern of the <i>IGL</i> locus on Southern blot.^{26, 49} Conversely the PCR assay failed to detect clonal rearrangements which were seen by Southern blot analysis in two cases (GBS-6, FR-5). However these were follicular lymphomas in which a high degree of somatic hypermutations may have prevented annealing of the <i>IGL</i> gene primers.

Conclusion

0125In conclusion, a single-tube PCR assay for the detection of <i>IGL</i> gene rearrangements containing only three primers (<figref idref="f0008">Figure 6B</figref>) allows to detect the vast majority of <i>IGL</i> gene rearrangements (Vλ1, Vλ2, and V3 gene rearrangements). Heteroduplex analysis is the preferred analytic method, though GeneScan analysis can be used, but maximal caution is recommended to avoid overinterpretation of clonality due to the limited junctional diversity.

EXAMPLE 5: <i>TCRB</i> gene rearrangements: V

β-

J

β,

D

β-

J

β

Background

0126Molecular analysis of the <i>TCRB</i> genes is an important tool for assessment of clonality in suspect T-cell proliferations. <i>TCRB</i> gene rearrangements occur not only in almost all mature T-cell malignancies but also in about 80% of the CD3 negative T-cell acute lymphoblastic leukemias (T-ALL) and 95% of the CD3 positive T-ALL.²⁸<i>TCRB</i> rearrangements are not restricted to T-lineage malignancies as about one third of precursor-B-ALL harbor rearranged <i>TCRB</i> genes.³⁰ Their frequency is much lower (0 to 7%) in mature B cell proliferations.²¹

0127The human <i>TCRB</i> locus is located on the long arm of chromosome 7, at band 7q34 and spans a region of 685 kb. In contrast to the <i>TCRG</i> and <i>TCRD</i> loci the V region gene cluster of the <i>TCRB</i> locus is far more complex (<figref idref="f0009">Figure 7A</figref>).¹ It contains about 65 Vβ gene elements for which two different nomenclatures are used: the one summarized by Arden et al.⁵⁰ follows the gene designation of Wei et al.⁸⁸ and groups the Vβ genes into 34 families. The alternative nomenclature proposed by Rowen et al.⁵¹ subdivides 30 Vβ gene subgroups and was later adopted by IMGT, the international ImMunoGeneTics database <u>http://imgt.cines.fr</u> (initiator and coordinator: Marie-Paule Lefranc, Montpellier, France). [Lefranc, 2003 #212;Lefranc, 2003 #219] The largest families, Vβ5, Vβ6, Vβ8 and Vβ13 (Arden nomenclature) reach a size of seven, nine, five and eight members, respectively. Twelve Vβ families contain only a single member. In general, the families are clearly demarcated from each other.⁵⁰ In this report we follow the Arden nomenclature. ⁵⁰

012839-47 of the Vβ gene elements are qualified as functional and belong to 23 families. 7-9 of the nonfunctional Vβ elements have an open reading frame but contain alterations in the splice sites, recombination signals and/or regulatory elements. 10-16 are classified as pseudogenes. In addition, a cluster of six non-functional orphan Vβ genes have been reported that are localized at the short arm of chromosome 9 (9p21).^{89, 90} They are not detected in transcripts.^{50, 51} All but one Vβ genes are located upstream of two Dβ-Jβ-Cβ clusters. <figref idref="f0009">Figure 7A</figref> illustrates that both Cβ gene segments (Cβ1 and Cβ2) are preceded by a Dβ gene (Dβ1 and Dβ2) and a Jβ cluster which comprises six (Jβ1.1 to Jβ1.6) and seven (Jβ2.1 to Jβ2.7) functional Jβ segments. Jβ region loci are classified into two families according to their genomic localization, not to sequence similarity.^{51, 68, 91}

0129Due to the large germline encoded repertoire, the combinatorial diversity of <i>TCRB</i> gene rearrangements is extensive compared to the <i>TCRG</i> and <i>TCRD</i> rearrangements. The primary repertoire of the TCRβ molecules is further extended by an addition of an average of 3.6 (V-D junction) and 4.6 (D-J junction) nucleotides and deletion of an average of 3.6 (V), 3.8 (5'of D), 3.7 (3'of D) and 4.1 (J) nucleotides.⁵¹ The complete hypervariable region resulting from the junction of the V, D and J segments comprises characteristically nine or ten codons. Size variation is limited, as 7 to 12 residues account for more than 80% of all functional rearrangements in contrast to the broad length repertoire of the <i>IGH</i> CDR3 region.⁹²

0130During early T-cell development the rearrangement of the <i>TCRB</i> gene consists of two consecutive steps: Dβ to Jβ rearrangement and Vβ to D-Jβ rearrangement with an interval of one to two days between these two processes.⁹³ The Dβ1 gene segment may join either Jβ1 or Jβ2 gene segments but the Dβ2 gene segment generally joins only Jβ2 gene segments because of its position in the <i>TCRB</i> gene locus.^{28, 51} Due to the presence of two consecutive <i>TCRB</i> D-J clusters, it is also possible that two rearrangements are detectable on one allele: an incomplete <i>TCRB</i> Dβ2-Jβ2 rearrangement in addition to a complete or incomplete rearrangement in the <i>TCRB</i> Dβ1-Jβ1 region.¹

0131In <i>TCRB</i> gene rearrangements, a non-random distribution of gene segment usage is seen. In healthy individuals, some Vβ families predominate in the peripheral blood T-cell repertoire (e.g Vβ1-Vβ5), while others are only rarely used (e.g. Vβ11, Vβ16, Vβ18, Vβ23). Mean values of the Vβ repertoire seem to be stable during aging, although the standard deviation increase in the elderly.^{13, 94} Also in the human thymus some Vβ gene segments dominate: the most prevalent seven Vβ genes (Vβ3-1, Vβ4-1, Vβ5-1, Vβ6-7, Vβ7-2, Vβ8-2, Vβ13-2) cover nearly half of the entire functional <i>TCRB</i> repertoire.⁸⁵ The representation of J segments is also far from even. The Jβ2 family is used more frequently than the Jβ1 family (72% vs. 28% of <i>TCRB</i> rearrangements).⁹⁸ In particular, the proportion of Jβ2.1 is higher than expected (24%) followed by Jβ2.2 (11%) and Jβ2.3 and Jβ2.5 (10% each).⁹⁵

0132<i>TCRB</i> gene rearrangement patterns differ between categories of T cell malignancies. Complete <i>TCRB</i> Vβ-Jβ1 rearrangements and incompletely rearranged alleles in the <i>TCRB</i> Dβ-Jβ2 cluster are seen more frequently in TCRαβ⁺ T-ALL as compared to CD3^- T-ALL and TCRγδ⁺ T-ALL.²⁸ In the total group of T-ALL the <i>TCRB</i> Dβ-Jβ1 region is relatively frequently involved in rearrangements in contrast to cross-lineage <i>TCRB</i> gene rearrangements in precursor-B-ALL which exclusively involve the <i>TCRB</i> Dβ-Jβ2 region.^{30, 73}

0133The development of monoclonal antibodies against most Vβ domains has helped to identify Vβ family expansions.¹³ However, TCR gene rearrangement analysis is essential for clonality assessment in T cell lymphoproliferative disorders. As the restricted germline encoded repertoire of the <i>TCRG</i> and <i>TCRD</i> loci facilitates DNA based PCR approaches, various PCR methods have been established for the detection of <i>TCRG</i> and <i>TCRD</i> gene rearrangements.^97-99 Nevertheless, the limited junctional diversity of <i>TCRG</i> rearrangements leads to a high background amplification of similar rearrangements in normal T cells (Example 6). The <i>TCRD</i> gene on the other hand is deleted in most mature T cell malignancies.²¹ Therefore DNA based <i>TCRB</i> PCR techniques are needed for clonality assessment. In addition, <i>TCRB</i> rearrangements are of great interest for follow-up studies of lymphoproliferative disorders, because the extensive combinatorial repertoire of <i>TCRB</i> rearrangements and the large hypervariable region enables a highly specific detection of clinically occult residual tumor cells. However, the extensive germline encoded repertoire renders PCR assays more difficult. Some published PCR approaches use the time consuming procedure of multiple tube approaches with a panel of family- or subfamily-specific primers.^{96, 100} Usage of highly degenerated consensus primers limits the number of detectable rearrangements that are theoretically covered by the primers because there is no single common sequence of sufficient identity to allow a reliable amplification of all possible rearrangements.^{42, 101, 102} Some published assays use a nested PCR requiring an additional PCR reaction.^{42, 102} Other assays focus on analysis of the <i>TCRB</i> Vβ-Dβ-Jβ-Cβ transcripts to limit the number of primers needed.^{16, 100, 103} However, a major drawback of these mRNA based approaches is the need for fresh or frozen material and a reverse transcription step before the PCR amplification.

0134We tried to overcome these limitations by creating a completely new and convenient DNA based <i>TCRB</i> PCR. We designed multiple Vβ and Jβ primers, covering all functional Vβ and Jβ gene segments and being suitable for combination in multiplex PCR reactions. In addition the assay is applicable for HD and GS analysis and also detects the incomplete <i>TCRB</i> Dβ-Jβ rearrangements with the same set of Jβ primers. In order to avoid problems due to cross priming we decided to design all Vβ and Jβ primers at the same conserved region of each gene segment.

Primer design

0135Initially a total of 23 Vβ, 2 Dβ (Dβ1 and Dβ2) and 13 Jβ (Jβ1.1 to 1.6 and Jβ2.1 to 2.7) primers were designed with all the Vβ and Jβ primers positioned in the same conserved region of each Vβ and Jβ gene segment so that the effects of cross-annealing in a multiplex reaction could be neglected. In addition, rare polyclonal <i>TCRB</i> V-J rearrangements would not be mistaken for a clonal rearrangement even if they do not produce a fully polyclonal Gaussian peak pattern, because PCR products of all possible rearrangements are situated in the same size range.

0136For primer design, the rearrangeable pseudogenes or open reading frame genes with alterations in splicing sites, recombination signals and/or regulatory elements or changes of conserved amino acids were taken into consideration whenever possible. However, the main objective was to cover all functional Vβ genes. The priming efficiency of each Vβ primer was checked for every Vβ gene using OLIGO 6.2 software. This led to primers that were not strictly Vβ family specific and some of which covered Vβ gene segments of more than one family (<figref idref="f0009">Figure 7B</figref>). Since the 13 Jβ primers annealed to the same segment of each Jβ gene primer, dimerization made it necessary to split the J primers into two tubes. Initially, it was planned to use the primers in four sets of multiplex reactions as follows: all 23 Vβ primers in combination with the six Jβ1 family primers (240-285 bp), all 23 Vβ primers with the seven Jβ2 family primers (240-285 bp), Dβ1 (280-320 bp) with the six Jβ1 primers, and Dβ1 (280-320 bp) plus Dβ2 (170-210 bp) with the seven Jβ2 family primers.

Results of initial testing phase

0137Initial monoplex testing of each possible primer combination was done using samples with known monoclonal <i>TCRB</i> rearrangements and polyclonal controls. PCR products of the expected size range were generated with differences in product intensity and signal profile for polyclonal samples depending on the frequency of usage of distinct Vβ and Jβ gene segments. However, when the primers were combined in a multiplex reaction some Jβ2 rearrangements in particular were missed and nonspecific products in the tubes B and D were observed. In addition cross-priming between the Jβ1 and Jβ2 primers resulted in interpretation problems. As a consequence the Jβ2 primers had to be redesigned and the primer combinations in the different tubes had to be rearranged: Jβ primers Jβ2.2, 2.6 and 2.7 were slightly modified and added to tube A. The localization of the primers Jβ2.1, 2.3, 2.4 and 2.5 was shifted by 4 bp downstream to avoid primer dimerization and cross priming with the remaining Jβ primers. Only nonspecific bands with varying intensity outside the expected size range persisted in tube B (bands&lt;150 bp, 221 bp) and tube C (128 bp, 337 bp) using specific template DNA. However, because all nonspecific amplification products were outside the size ranges of the <i>TCRB</i> specific products, they did not affect interpretation and were considered not to be a problem. However, using nonspecific template controls one additional faint 273 bp aspecific peak in tube A was visible by GS analysis. This product is completely suppressed when the DNA contains enough clonal or polyclonal <i>TCRB</i> rearrangements but can appear in samples comprising low numbers of lymphoid cells. In the initial testing phase relatively faint V-D-J PCR products were generated. Thus we optimized PCR conditions for complete V-D-J rearrangements by increasing MgCl₂ concentration and the amount of Taq polymerase. Also usage of highly purified primers and application of ABI Buffer II instead of ABI Gold Buffer turned out to be very important. For detection of the incomplete Dβ-Jβ rearrangements, it was finally possible to mix all Jβ primers into one tube without loss of sensitivity or information. Consequently, the total number of multiplex reactions could be reduced to three tubes.

0138The finally approved primer set is (<figref idref="f0009">Figure 7B</figref>): <tables id="tabl0001" num="0001"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="16mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><tbody><row><entry><b>tube A:</b></entry><entry>23 Vβ primers and 9 Jβ primers: Jβ1.1-1.6, 2.2, 2.6 and 2.7</entry></row><row><entry><b>tube B:</b></entry><entry>23 Vβ primers and 4 Jβ primers: Jβ2.1, 2.3, 2.4 and 2.5</entry></row><row><entry><b>tube C:</b></entry><entry>Dβ1, Dβ2 and all 13 Jβ primers.</entry></row></tbody></tgroup></table></tables> As tubes A and C contain Jβ1 and Jβ2 primers, differential labeling of Jβ1 and Jβ2 primers with different dyes (TET for Jβ1.1-1.6 and FAM for Jβ2.1-2.7 primers) allows GS discrimination of Jβ1 or Jβ2 usage in tube A and C reactions (see <figref idref="f0016">Figure 13A</figref>).

0139Sensitivity testing was performed via dilution experiments with various cell lines and patient samples with clonally rearranged <i>TCRB</i> genes in MNC. Single PCR dilution experiments generally reached sensitivity levels of at least 0.1% to 1%. As expected, the sensitivity decreased in multiplex testing, probably due to an increase of background amplification. Especially in GS analysis this background hampered interpretation due to the relative small length variation of the <i>TCRB</i> PCR products. Nevertheless, in 40 of 46 positive controls tested a sensitivity of at least 1% to 10% was reached using heteroduplex or GeneScanning (Table 6).

Results of general testing phase

0140Eleven groups participated in the analysis of DNA from a series of 90 Southern blot-defined malignant and reactive lymphoproliferative disorders using the <i>TCRB</i> multiplex protocol. Every sample was analysed by HD in two laboratories and in six laboratories using GS analysis. Another three laboratories used both techniques for PCR analysis (<figref idref="f0010">Figure 7C</figref>, D, and E). This testing phase as well as experience from use of these <i>TCRB</i> PCR assays raised some general issues about the protocol that were in part already described in the initial testing phase: 1. The limited length variation of the <i>TCRB</i> PCR products may hamper GS detection of clonal signals within a polyclonal background. 2. Only bands/peaks within the expected size range represent clonal <i>TCRB</i> gene rearrangements. Especially for tube A a nonspecific control DNA must be included to define the aspecific 273 bp peak that may occur in situations without competition. 3. It is extremely important to use highly purified primers and ABI Buffer II (and not ABI Gold Buffer) for good PCR results as well as the recommended PCR product preparation protocol for HD analysis. Of the 90 Southern blot-defined cases submitted, 29 were SB positive for monoclonal <i>TCRB</i> rearrangements. 25 of these clonal rearrangements (86%) were also detectable by the <i>TCRB</i> PCR. 23 rearrangements were disclosed by GS and HD analysis, two additional cases only by HD. One of the GS negative HD positive cases (FR-9) was interpreted as monoclonal on GS analysis by four of the nine laboratories involved in the general testing phase (<figref idref="f0010">Figure 7C</figref>). However, due to a significant polyclonal background, interpretation of the GS patterns was difficult in this particular case. The other GS negative HD positive case displayed an atypical PCR product in tube C with a size of about 400 bp (<figref idref="f0010">Figure 7E</figref>). The PCR product was clearly visible in agarose gels and HD analysis but not by GS. After DNA sequencing of this fragment a <i>TCRB</i> Dβ1-Dβ2 amplification product was identified explaining the unlabelled PCR product. Four SB positive cases (NL-15, NL-16, GBN-2 and FR-6) were neither detected by GS nor by HD analysis all of them with an underlying B lymphoid malignancy. Possible explanations for this failure are atypical rearrangements (e.g. incomplete Vβ-Dβ rearrangements),^{28, 104} sequence variations of the rearranged Vβ gene segments⁵¹ or a lack of sensitivity for particular rearrangements.

014162 of the samples were considered to be polyclonal by SB. For 61 (98%) of these cases PCR results were concordant with at least one method of analysis, for 57 (92%) cases results were concordant using both methods. The one SB negative sample (ES-14) found to be monoclonal by HD and GS analysis showed an incomplete Dβ2-rearrangement. For four samples non-uniform results were obtained: one sample was considered to be clonal by GS but only by 50% of the labs analyzing the PCR products by HD (GBS-4). Three samples were found to produce weak clonal signals only by HD analysis (ES-6, GBS-9 and DE-2). <i>TCRB</i> rearranged subclones being too small to be detected by SB analysis may only be seen by the more sensitive PCR methodology. In B cell malignancies the detected rearrangements may also represent clonal or oligoclonal expansions of residual T cells.¹⁰⁵ In this case these weak clonal PCR products should not be regarded as evidence of a clonal T cell disorder. This stresses the importance of the interpretation of the PCR results in context with other diagnostic tests and the clinical picture of the patients. Optimal PCR assessment of <i>TCRB</i> rearrangements is obtained by the combined use of HD and GS analysis. Sensitivity may differ between the two detection methods as a function of clonal PCR product size compared to the polyclonal size distribution: on the one hand HD analysis disperses the polyclonal background from the clonal products and on the other hand PCR products outside the main size range allow a more sensitive GS detection. Also the risk of false-positive results is reduced in the combined use of HD and GS analysis. Furthermore, HD analysis allows detection of some additional atypical <i>TCRB</i> Dβ1-Dβ2 rearrangements that cannot be detected by GS analysis of the PCR product as no labeled primer is involved in amplification. However, GS analysis is in general the more informative method for samples with a high tumor load because the exact size of the monoclonal PCR product is indicated, which may be used for monitoring purposes and differentially labeled Jβ primers provide additional information about Jβ gene usage.

Conclusion

0142In conclusion, the three-tube <i>TCRB</i> multiplex PCR system provides a new and convenient assay for clonality assessment in suspect T-cell proliferations with an unprecedentedly high clonality detection rate.

EXAMPLE 6: <i>TCRG</i> gene rearrangements

Background

0143<i>TCRG</i> gene rearrangements have long been used for DNA PCR detection of lymphoid clonality and represent the "prototype" of restricted repertoire targets. It is a preferential target for clonality analyses since it is rearranged at an early stage of T lymphoid development, probably just after <i>TCRD</i>,¹⁰⁶ in both TCRαβ and TCRγδ lineage precursors. It is rearranged in greater than 90% of T-ALL, T-LGL and T-PLL, in 50-75% of peripheral T-NHL and mycosis fungoides but not in true NK cell proliferations. It is also rearranged in a major part of B lineage ALLs, but much less so in B-NHL.^{1, 30, 73} Unlike several other Ig/TCR loci, the complete genomic structure has been known for many years. It contains a limited number of Vγ and Jγ segments. Amplification of all major Vγ-Jγ combinations is possible with limited number of four Vγ and three Jγ primers.

0144The human <i>TCRG</i> locus on chromosome 7p14 contains 14 Vγ segments, only ten of which have been shown to undergo rearrangement (<figref idref="f0011">Figure 8A</figref>). The <i>expressed</i> Vγ repertoire includes only six Vγ genes (Vγ2, Vγ3, Vγ4, Vγ5, Vγ8 and Vγ9) but rearrangement also occurs with the ψVγ7, ψVγ10, γψVγ11 segments.^{107, 108} Rearrangement of ψVγB (also known as Vγ12) ¹⁰⁷ is so exceptional that it is rarely used in diagnostic PCR strategies. Rearranging Vγ segments can be subdivided into those belonging to the VγI family (VγfI: Vγ2, Vγ3, Vγ4, Vγ5, ψVγ7 and Vγ8; overall homology > 90% and highest between Vγ2 and Vγ4 and between Vγ3 and Vγ5) and the single member Vγ9, ψVγ10, ψVγ11 families. The <i>TCRG</i> locus contains five Jγ segments: Jγ1.1 (JγP1), Jγ1.2 (JγP), Jγ1.3 (Jγ1), Jγ2.1 (JγP2), Jγ2.3 (Jγ2), of which Jγ1.3 and Jγ2.3 are highly homologous, as are Jγ1.1 and Jγ2.1.¹⁰⁹

0145Whilst the restricted <i>TCRG</i> germline repertoire facilitates PCR amplification, the limited junctional diversity of <i>TCRG</i> rearrangements complicates distinction between clonal and polyclonal PCR products. The <i>TCRG</i> locus does not contain D segments and demonstrates relatively limited nucleotide additions. <i>TCRG</i> V-J junctional length therefore varies by 20-30 bp, compared to approximately 60 bp for <i>IGH</i> and <i>TCRD.</i> The capacity to distinguish clonal from polyclonal <i>TCRG</i> rearrangements depends on the complexity of the polyclonal repertoire. In general, minor clonal populations using frequent Vγ-Jγ rearrangements such as VγfI-Jγ1.3/2.3 are at risk of being lost amidst the polyclonal repertoire, whereas rare combinations will be detected with greater sensitivity. However, occasional polyclonal T lymphocytes demonstrating rare Vγ-Jγ rearrangements may be mistaken for a clonal rearrangement, due to absence of a polyclonal background for that type of rearrangement. A further possible source of false positivity results from the presence of TCRγδ expressing T lymphocytes demonstrating "canonical" <i>TCRG</i> rearrangements, which do not demonstrate N nucleotide additions. The most commonly recognized human canonical <i>TCRG</i> rearrangement involves the Vγ9-Jγ1.2 segments and occurs in approximately 1 % of blood T-lymphocytes.^{110, 111} It is therefore extremely important to analyze <i>TCRG</i> PCR products using high resolution electrophoretic techniques or to separate PCR products on criteria other than purely on size, in order to reduce the risk of false positive results. It is also important to be aware of the profile of canonical rearrangements and the situations in which they most commonly occur. Canonical Vγ9-Jγ1.2 rearrangements, for example, are found predominantly in peripheral blood and increase in frequency with age, since they result from accumulation of TCRγδ⁺ T-lymphocytes.¹⁹

0146Unlike <i>TCRD, TCRG</i> is not deleted in TCRαβ lineage cells. Since <i>TCRG</i> rearrangements occur in both TCRαβ and TCRγδ lineage precursors, their identification cannot be used for determination of the type of T cell lineage. Similarly, <i>TCRG</i> rearrangements occur in 60% of B lineage ALLs,³⁰ implying that they can not be used for assessment of B vs. T cell lineage in immature proliferations. However, they occur much less frequently in mature B lymphoproliferative disorders, including the majority of B-NHL,¹ and might therefore be used, in combination with clinical and immunophenotypic data, to determine lineage involvement in mature lymphoproliferative disorders.

0147The limited germline repertoire allows determination of Vγ and Jγ segment utilization, either by Southern blot or PCR analysis. Identification of Vγ and Jγ usage is not of purely academic interest, since specific amplification is required for MRD analysis.¹¹²

0148We undertook to develop a minimal number of multiplex <i>TCRG</i> strategies which would maintain optimal sensitivity and informativity, minimize the risk of false positive results and allow simple Vγ and Jγ identification, including by HD analysis or monofluorescent GS strategies. We chose to include Vγ primers detecting all rearranging segments other than ψVγB (ψVγ12), given its rarity. In order to reduce the risk of falsely identifying canonical rearrangements as clonal products, we excluded the Jγ1.2 primer, since it is rarely involved in lymphoid neoplasms and is usually, although not always, associated with a <i>TCRG</i> rearrangement on the other allele.¹¹³

Primer design

0149We initially developed 3Vγ and 2 Jγ primers, to be used in two multiplex reactions, as follows: one tube with Jγ1.3/2.3 with Vγ9 specific (160-190 bp), VγfI consensus (200-230 bp) and Vγ10/11 consensus (220-250 bp) and a second tube with Jγ1.1/2.1 with Vγ9 specific (190-220 bp), VγfI consensus (230-260 bp) and Vγ10/11 consensus (250-280bp). Vγ usage was to be identified by PCR product size by HD analysis. No distinction between Jγ1.3 and Jγ2.3 or Jγ1.1 and Jγ2.1 was attempted.

Results of initial testing phase

0150While all Vγ-Jγ combinations gave the expected profiles on single PCR amplification, multiplex amplification led to competition of larger PCR products, with preferential amplification of smaller fragments, and failure to detect some VγfI and Vγ10/11 rearrangements. This was further complicated by significant primer dimer formation between the Vγ10/11 consensus and the VγfI primers. Competition between differently sized fragments and primer dimer formation both led to unsatisfactory sensitivity and informativity and this strategy was therefore abandoned.

0151We reasoned that competition would be minimized by separating the most frequently used Vγ primers (VγfI and Vγ9) and combining them with Vγ10 and Vγ11 specific primers, respectively. The latter rearrangements are rarely used and therefore minimize competition for the predominant repertoires. The Vγ10/11 consensus primer was therefore replaced by two specific Vγ primers which generated smaller PCR products (<figref idref="f0011">Figure 8B</figref>). By mixing Jγ1.3/2.3 and Jγ1.1/2.1 it was possible to maintain a two-tube multiplex which allows approximate identification on the basis of product size of Vγ usage by HD analysis and of both Jγ and Vγ usage by GS analysis.

0152The approved set of multiplex <i>TCRG</i> PCR tubes with four Vγ and two Jγ primers includes (<figref idref="f0011">Figure 8B</figref>): <tables id="tabl0002" num="0002"><table frame="none"><tgroup cols="2" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="16mm" /><colspec colnum="2" colname="col2" colwidth="50mm" /><tbody><row><entry>Tube A:</entry><entry>VγfI + Vγ10 + Jγ1.1/2.1+ Jγ1.3/2.3</entry></row><row><entry>Tube B:</entry><entry>Vγ9 + Vγ11 + Jγ1.1/2.1+ Jγ1.3/2.3</entry></row></tbody></tgroup></table></tables>

0153The position and the sequence of the primers are shown in <figref idref="f0011">Figure 8B</figref>. These primers gave satisfactory amplification in both single and multiplex PCR formats and allowed detection of virtually all known Vγ-Jγ combinations. The competition of larger PCR fragments was no longer seen, although it cannot be excluded that some competition of Vγ9 or VγfI rearrangements may occur if these are present in a minority population.

0154Sensitivity of detection varied between 1% and 10%, as a function of the complexity of the polyclonal repertoire and the position of the clonal rearrangement relative to the polyclonal Gaussian peak.¹¹⁴ Interpretation of ψVγ11 rearrangements can be difficult, since the normal repertoire is extremely restricted and since these primitive rearrangements are often present in subclones.

0155Since the Vγ4 segment is approximately 40 bp longer than the other VγfI members and Vγ4 rearrangements are relatively common in both physiological and pathological lymphoid cells, the polyclonal repertoire can be skewed towards larger sized fragments, and clonal Vγ4-Jγ1.3/2.3 rearrangements could theoretically be mistaken for VγfI-Jγ1.1/2.1 rearrangements. The proximity of the different repertoires also makes Vγ and Jγ identification much more reliable if differently labeled Jγ primers are used. For example, the use of a TET-labeled Jγ1.1/2.1 and a FAM labeled Jγ1.3/2.3 was tested in a single center and was shown to give satisfactory results (<figref idref="f0016">Figure 13B</figref>). It is, however, possible to estimate Vγ and Jγ usage following GS analysis on the basis of size alone (<figref idref="f0011">Figure 8C and D</figref>).

Results of general testing phase

0156Given the limited germline <i>TCRG</i> repertoire and the restricted junctional diversity, reactive T lymphocytes which have undergone <i>TCRG</i> rearrangements using a single Vγ and Jγ segment with variable CDR3 sequences which are of uniform length, will migrate as an apparent clonal population by GS analysis. HD formation will disperse these rearrangements more easily and will therefore prevent their erroneous interpretation as evidence of lymphoid clonality. In contrast, GS analysis provides improved resolution and sensitivity compared to HD analysis. For these reasons, optimal assessment of <i>TCRG</i> rearrangements requires both HD and GS analysis. If this is not possible, HD analysis alone is probably preferable, since it might be associated with a risk of false-negative results, whereas GS analysis alone will increase the risk of false-positive results.

0157Of the 18 <i>TCRG</i> rearrangements detected by Southern blotting in the 90 cases , 16 were also detected by PCR. The minor Vγf1-Jγ1.3/2.3 rearrangement detected by Southern in the NL-1 oligoclonal case, was only detected by PCR in a proportion of laboratories performing GS analysis. A major Vγ9-Jγ1.3/2.3 rearrangement detected in GBS-6 was found to be polyclonal by both HD and GS in all laboratories and, as such, probably represents a false-negative result.

0158Comparison of allele identification showed that, for all alleles identified by Southern blotting, PCR Vγ and Jγ identification on the basis of size gave concordant results. Seven rearrangements were detected by Southern blotting but precise allele identification was not possible. Six of these were due to Jγ1.1/2.1 usage, suggesting that PCR allows preferential detection of this type of rearrangement.

0159Seventy two samples were considered to be polyclonal by Southern. Sixteen (22%) of these demonstrated a total of 24 rearrangements by <i>TCRG</i> PCR. Of these, 13 (81%) were B lymphoid proliferations. Sixteen of the 24 clonal rearrangements were minor, with 15 only being detected by GS in the majority of laboratories. It is worth noting that, of these minor rearrangements, nine (39%) involved the ψVγ10 segment and eight (33%) Vγ9. ψVγ11 rearrangements were not detected. No ψVγ10 rearrangements were detected by Southern blot analysis. PCR therefore allowed more sensitive detection of minor clonal ψVγ10 rearrangements, particularly by GS analysis. It is likely that these rearrangements represent residual, predominantly TCRαβ lineage, T lymphocytes with a restricted repertoire, which may or may not be related to the underlying B lymphoid malignancy. These minor peaks should obviously not be interpreted as evidence of a clonal T cell disorder. They emphasize the importance of understanding the nature of <i>TCRG</i> rearrangements before using this locus as a PCR target in the lymphoid clonality diagnostic setting. Consequently, it is also extremely important to interpret <i>TCRG</i> gene results within their clinical context.

Conclusion

0160In conclusion, the two <i>TCRG</i> multiplex tubes allow detection of the vast majority of clonal <i>TCRG</i> rearrangements. The potential risk of false positive results due to overinterpretation of minor clonal peaks can be minimized by the combined use of heteroduplex analysis and GeneScanning and by interpreting results within their clinical context, particularly when the apparent clonality involved the ψVγ10 and ψVγ11 segments. The relative merits of <i>TCRG</i> compared to <i>TCRB</i> analysis for the detection of clonal T lymphoproliferative disorders should be studied prospectively. They are likely to represent complementary strategies.

EXAMPLE 7. <i>TCRD</i> gene rearrangements: V

δ

-D

δ

-J

δ

, D

δ

-D

δ

, V

δ

-D

δ

, and D

δ

-J

δ

Background

0161The human <i>TCRD</i> gene locus is located on chromosome 14q11.2 between the Vα and Jα gene segments. The major part of the <i>TCRD</i> locus (Dδ-Jδ-Cδ) is flanked by <i>TCRD</i>-deleting elements, ψJα and δREC such that rearrangement of the deleting elements to each other or rearrangement of Vα to Jα gene segments causes deletion of the intermediate <i>TCRD</i> gene locus (<figref idref="f0012">Figure 9A</figref>). The germline encoded <i>TCRD</i> locus consists of 8Vδ, 4Jδ, and 3Dδ gene segments, of which at least five of the eight Vδ gene segments can also rearrange to Jα gene segments.¹¹⁵ Other Vα gene segments may also be utilized in <i>TCRD</i> gene rearrangements in rare cases. The WHO-IUIS nomenclature¹¹⁶ for TCR gene segments uses a different numbering system for those V genes used mainly or exclusively in TCRδ chains from those which can be used in either TCRα or TCRδ chains. Thus <i>TCRDV101S1</i> (Vδ1), <i>TCRDV102S1</i> (Vδ2) and <i>TCRDV103S1</i> (Vδ3) are used almost exclusively in <i>TCRD</i> rearrangements, whereas <i>TCRADV6S1</i> (Vδ4), <i>TCRADV21S1</i> (Vδ5) and <i>TCRADV17S1</i> (Vδ6) can be used in either TCRδ or α chains. <i>TCRADV28S1</i> (Vδ7) and <i>TCRADV14S1</i> (Vδ8) are used extremely rarely in <i>TCRD</i> rearrangements.

0162The germline-encoded repertoire of the TCRγδ⁺ T cells is small compared to the TCRαβ⁺ T cells and the combinatorial repertoire is even more limited due to preferential recombination in peripheral blood and thymocyte TCRγδ⁺ T cells. At birth, the repertoire of cord blood TCRγδ⁺ T cells is broad, with no apparent restriction or preferred expression of particular Vγ/Vδ combinations. During childhood, however, the peripheral blood TCRγδ⁺ T cell repertoire is strikingly shaped so that Vγ9/Vδ2 cells clearly dominate in adults.¹¹⁷ Studies have shown that Vδ1 and Vδ2 repertoires become restricted with age leading to the appearance of oligoclonal Vδ1⁺ and Vδ2⁺ cells in blood and intestine.¹¹⁰ TCRγδ⁺ T cells are evenly distributed throughout human lymphoid tissues but there is preferential expression of particular Vδ segments in specified anatomical localizations. Notably, most intraepithelial TCRγδ T cells occurring in the small intestine and in the colon express Vδ1. Similarly, Vδ1 is expressed by normal spleen TCRγδ⁺ T cells, but TCRγδ⁺ T cells in the skin express the Vδ2 gene.

0163Although the small number of V, D and J gene segments available for recombination limits the potential combinatorial diversity, the CDR3 or junctional diversity is extensive due to the addition of N regions, P regions and random deletion of nucleotides by recombinases. This diversity is also extended by the recombination of up to three Dδ segments and therefore up to four N-regions within the rearranged <i>TCRD</i> locus. This limited germline diversity encoded at the <i>TCRD</i> locus in conjunction with extensive junctional diversity results in a useful target for PCR analysis and <i>TCRD</i> recombination events have been used most extensively as clonal markers in both T and B cell acute lymphoblastic leukemia (ALL).^{119, 120} The <i>TCRD</i> locus is the first of all TCR loci to rearrange during T cell ontogeny. The first event is a Dδ2-Dδ3 rearrangement, followed by a Vδ2-(Dδ1-Dδ2)-Dδ3 rearrangement, and finally Vδ-Dδ-Jδ rearrangement. Immature rearrangements (Vδ2-Dδ3 or Dδ2-Dδ3) occur in 70% of precursor B-ALL (and are therefore non lineage restricted)³⁰ while there is a predominance of mature rearrangements comprising incomplete Dδ2-Jδ1 and complete Vδ1, Vδ2, Vδ3 to Jδ1 found in T-ALL.^{23, 121} Thus specific primer sets can be used to identify different types of complete and incomplete rearrangements corresponding to different types of ALL.¹²²

0164TCRγδ⁺ T-ALL form a relatively small subgroup of ALL, representing 10-15% of T-ALL but still only constitute 2% of all ALL. Vδ1-Jδ1 rearrangements predominate in TCRγδ⁺ T ALL; interestingly Vδ1 is never found in combination with Jδ segments other than Jδ1.^{15, 20} Other recombinations occur in less than 25% of alleles. Furthermore, Vδ1-Jδ1-Cδ chains are almost always disulfide linked to either VγI or VγII gene families recombined to Jγ2.3-Cγ2. Such gene usage is consistent with the immature thymic origin of these leukemic cells.

0165Most T cell lymphomas express TCRαβ while the minority express TCRγδ and comprise of several distinct entities. Peripheral T cell lymphomas (PTCL) expressing TCRγδ comprise 8-13% of all PTCL and Vδ1-Jδ1 as well as other Vδ to Jδ1 recombinations have been documented.^{123, 124} Hepatosplenic γδ T-cell lymphoma is derived from splenic TCRγδ T cells which normally express Vδ1. It is an uncommon entity that exhibits distinctive clinicopathologic features and gene usage analysis has indicated clonal Vδ1-Jδ1 rearrangements associated with these lymphomas.¹²⁵ Furthermore, the rare type of cutaneous TCRγδ⁺ T cell lymphomas express Vδ2 and therefore appear to represent a clonal expansion of TCRγδ⁺ T cells which normally reside in the skin.¹²⁶ Other clonal TCRγδ proliferations include CD3⁺ TCRγδ⁺ large granular lymphocyte (LGL) proliferations which comprise about 5% of all CD3⁺ LGL and often show Vδ1-Jδ1 rearrangements.¹²⁷

0166The development of monoclonal antibodies towards framework regions of TCRγδ and more recently to specific Vδ gene segments has helped identify TCRγδ⁺ T cell populations by flow cytometric analysis,¹⁵ but PCR clonality studies are still required to identify whether these populations represent clonal or polyclonal expansions.¹²⁸

Primer design

0167The <i>TCRD</i> gene segments, consisting of eight Vδ, four Jδ and three Dδ gene segments, show little or no homology to each other and so segment-specific primers were designed which would not cross-anneal with other gene segments. Usage of Vδ7 and Vδ8 gene segments was considered too rare to justify inclusion of primers for these segments and so, following the general guidelines used in the invention for primer design, a total of 16 primers were designed: 6 Vδ, 4 Jδ and 5' and 3' of the 3 Dδ gene segments (<figref idref="f0012">Figure 9B</figref>). All primers were designed for multiplex together in any combination, but originally it was planned to have one tube (A) with all V and all J primers which would amplify all the complete V(D)J rearrangements and a second tube (B) with Vδ2, Dδ2-5', Dδ3-3' and Jδ1 primers to amplify the major partial rearrangements (Vδ2-Dδ3, Dδ2-Dδ3 and Dδ2-Jδ1). Together these tubes should amplify 95% of known rearrangements. The other primers (Dδ1-5', Dδ3-5', Dδ1-3' and Dδ2-3') could be used to amplify other Dδ-Jδ, Vδ-Dδ or Dδ-Dδ rearrangements, but were always intended to be optional.

Results of initial testing phase

0168All primer pair combinations were tested using polyclonal DNA (tonsil and MNC). Most gave products of the expected size, but some (Dδ1-5', Dδ1-3' and Dδ2-3') gave no visible product in combination with any other primer. Rearrangements involving these primer regions are likely to be extremely rare and so these; and Dδ3-5', were excluded from subsequent testing. Clonal cases for the six main rearrangements (Vδ1-Jδ1, Vδ2-Jδ1, Vδ3-Jδ1, Dδ2-Dδ3, Vδ2-Dδ3 and Dδ2-Jδ1) were tested initially in monoplex PCR and then in multiplex tubes A and B (see above). Serial dilutions of clonal DNA in polyclonal DNA (tonsil or MNC) showed detection sensitivities of at least 5% in all cases. However, in clonal cases with biallelic rearrangements, which were clearly detected in single PCR reactions, the second, usually larger, allele often failed to amplify on multiplexing. In addition, it was found, using a different set of clonal cases that several of the Vδ2-Jδ1 rearrangements failed to amplify. A polymorphic site was subsequently identified at the position of the original Vδ2 primer;¹²⁹ the frequency of this polymorphism in the general population unknown, and so this primer was redesigned to a new region of the Vδ2 gene segment, retested and found to amplify all cases. The problem with the failure to amplify the second allele was overcome by increasing the MgCl₂ concentration from 1.5 mM to 2.0 mM.

0169We also tested the possibility of combining the two tubes into a single multiplex reaction. Twelve clonal cases were tested, which had a total of 21 gene rearrangements between them. A single multiplex tube containing 12 primers (6 Vδ, 4 Jδ, Dδ2-5' and Dδ3-3') was used with ABI Gold buffer and 2.0 mM MgCl₂ to amplify all the cases. All gene rearrangements were indeed detected with a sensitivity of 0.5-10% by HD analysis when diluted in polyclonal MNC DNA (Table 7). The only problem with combining all <i>TCRD</i> primers in a single tube was the appearance of a nonspecific band at about 90 bp in all amplifications, which was not present when the two separate multiplex tubes were used. Since the band was outside the size range of the <i>TCRD</i> products and did not interfere with interpretation, it was not considered to be a problem.

Results of general testing phase

0170The testing of the 90 Southern blot-defined samples in ten laboratories raised some general issues about the <i>TCRD</i> protocol: Interpretation of some GS results was difficult. Because of the large size range of products for the <i>TCRD</i> locus, there is no classical Gaussian distribution for polyclonal samples (see <figref idref="f0012">Figure 9C</figref>) and this, coupled with the low usage of <i>TCRD</i> in many samples meant that in some cases it was hard to determine whether a sample was polyclonal or clonal. The same problem did not arise with HD analysis and so the recommendation is that GS should only be used for <i>TCRD</i> with extreme care and awareness of the potential problems. The 90 bp nonspecific band was quite intense in some laboratories, but less so in others. It appeared to be weaker when using Buffer II rather than Gold buffer (confirmed by subsequent testing) and is also sensitive to MgCl₂ concentration, becoming more intense as MgCl₂ concentration increases. This product has now been sequenced and found to be an unrelated gene utilizing the Dδ2 and Jδ3 primers.

0171The results of the general testing of the 90 Southern blot defined samples showed that the overall concordance of all the PCR groups doing the testing was very high (95%). Of the 90 cases, six were Southern blot positive for <i>TCRD</i> clonal rearrangements, five of which were found to be clonal by PCR. The remaining case (DE-10, a T-ALL with high tumor load) was found to be polyclonal by all labs. Of the 84 Southern blot negative cases, 75 were found to be polyclonal by PCR, four were found to be clonal and the remaining five cases showed discordance between the GS and HD results. Of the clonal cases, two (DE-2 and GBS-9) were T-rich B-NHLs with presumably low tumor load and so the results may reflect the increased sensitivity of PCR over Southern blotting. The other two clonal cases (GBS-15 and ES-7) had high tumor load. Of the five cases, which showed discrepancy between the GS and HD results, one (NL-1) was a difficult oligoclonal case, which caused problems for several other loci. The remaining four were found to be polyclonal by HD and clonal by GS. In three of the cases (NL-13, NL-15 and NL-18) this may reflect the greater sensitivity of GS over HD analysis, but the remaining case (PT-1, a reactive lymph node) may be attributed to "pseudoclonality" on GS analysis because of the limited repertoire of <i>TCRD</i> usage in some samples.

Conclusion

0172In conclusion, the recommended protocol for detection of <i>TCRD</i> gene rearrangements is a single tube assay containing 12 primers for detection of all major Vδ(D)Jδ, Vδ-Dδ, Dδ-Dδ and Dδ-Jδ rearrangements using Buffer II and 2.0 mM MgCl₂ to ensure maximum specificity and detection. The preferred analysis method is HD, but GS may be used with care if consideration is given to the problems of pseudoclonality caused by the limited usage of <i>TCRD</i> in some samples. However, the use of multi-color GeneScanning (see <figref idref="f0016">Figure 13C</figref>) can be helpful in rapid recognition of the different types of complete and incomplete <i>TCRD</i> gene rearrangements in the different types of ALL. With these limitations in mind, <i>TCRD</i> can nevertheless be a valuable target for the more immature T-cell leukemias as well as TCRγδ⁺ T-cell proliferations.

EXAMPLE 8. t(11;14) with <i>BCL1-IGH</i> rearrangement

Background

0173The t(11;14)(q13;q32) is characteristic for mantle cell lymphoma (MCL) because this cytogenetic reciprocal translocation was observed in 60-70% of MCL cases and only sporadically in other B-cell NHL.¹³⁰ The breakpoint region was originally cloned by Tsujimoto et al (1983) and referred to as the <i>BCL1</i>-region.¹³¹ However in only few cases with a cytogenetic t(11;14) a genomic breakpoint in the <i>BCL1</i>-region was identified. Using fiber and interphase FISH with probes covering the approximately 750 kb 11q13-<i>BCL1</i> region, in almost all MCL (33 out of 34) a breakpoint was observed and all breakpoints were confined to a region of 360 kb 5' of the cyclin D1 gene.^{132, 133} In nearly half of MCL cases (41%) the breakpoints were clustered within an 85 bp region that was referred to as the major translocation cluster region, <i>BCL1</i>-MTC.^{130, 134, 135} In most if not all cases of MCL the break at the <i>IGH</i> locus located at 14q32 involves the J_H genes juxtaposing the <i>IGH-</i>Eµ enhancer to chromosome 11q13 sequences and consequently resulting in transcriptional activation of the cyclin D1 gene.¹³⁶ Cyclin D1 together with CDK4 phosphorylates (and inactivates) pRB and allows for progression through the G1 phase of the cell cycle. Because cyclin D1 is silent in B-lymphocytes and B-cell NHL other than MCL, and the presence of this translocation correlates well with cyclin D1 expression, this gene is considered to be the biological relevant target in MCL.¹³⁶ Both expression of cyclin D1 and/or the presence of t(11;14)(q13;q32) is used as an additional tool in the differential diagnosis of NHL.² The gold standard detection strategy for the presence of the t(11;14) that will identify almost all breakpoints is interphase FISH using breakpoint-flanking probes in fresh or frozen material¹³³ as well as in archival specimens.¹³⁷ However, a PCR based detection strategy for the t(11;14) might be useful for e.g. residual disease monitoring. Many groups have developed PCR based assays to detect the BCL1/JH-breakpoints, in general using a consensus JH-primer in combination with primers in the <i>BCL1</i>-MTC region that were all located in a region of 392 bp.^54,55 Breaks within the <i>BCL1</i>-MTC region can occur upto 2 kb downstream of the MTC region, but the majority of breakpoints are tightly clustered within an 85 bp segment, immediately downstream of the reported most 3'-primer ("primer B" in ^{54, 134}). Because breaks in this <i>BCL1</i>-MTC-region account for only part of the breakpoints in the 11q13-<i>BCL1</i> region in MCL cases (41%), the PCR based strategy for t(11;14) seriously impairs the diagnostic capability with an high rate of false-negative results as compared to FISH.

0174The t(11;14)(q13;q32) has also been reported to be observed in other B-cell proliferative diseases such as multiple myeloma (20%), SLVL (30%), B-PLL (33%) and B-CLL (8%).^{130, 138, 139} One reason for the presence of the t(11;14) in B-CLL in some studies might be due to the incorrect classification of B-CLL.¹³⁰ In myeloma the breakpoints are quite different from those in MCL because (i) the frequency is much lower; (ii) most breaks involve switch-class recombination sites; and (iii) although all tested cases are located in the same 360 kb <i>BCL1</i>-region there seems to be no preferential clustering within the <i>BCL1</i>-MTC region. On the other hand, in all cases with a break the cyclin D1 gene is activated. Of note, in a subgroup of multiple myelomas with a <i>IGH</i>-switch-break <i>myeov</i>, an additional region in the 11q13-<i>BCL1</i> region, is involved.¹³⁸

Primer design

0175Based on the location of the reported most-far 5'-breakpoint and available nucleotide sequences from the <i>BCL1</i>-MTC region (GenBank accession number S77049), we designed a single <i>BCL1</i> primer (5'-GGATAAAGGCGAGGAGCATAA-3') in the 472-bp region 5' of this breakpoint by using the primer design program OLlGO6.2 relative to the consensus JH primer.

Results of initial testing phase

0176Using the consensus JH-primer in combination with the single <i>BCL1</i>-MTC-primer on a small series of MCL (n=5) previously identified as positive with an in-house BCL1/JH-PCR using a similar consensus JH18-primer (18 nt) and 5'-GCACTGTCTGGATGCACCGC-3' as <i>BCL1</i>-MTC-primer, we initially compared both assays in parallel. In contrast to the analysis of Ig/TCR gene rearrangements via GS and/or HD analysis, the <i>BCL1</i>-JH PCR products (as for <i>BCL2</i>-JH products) are identified via agarose gel electrophoresis using ethidium bromide staining only. The results on the five positive and two negative samples were identical except that the PCR products were significantly weaker. To evaluate whether we could increase the sensitivity of the PCR, we determined the effect of different concentrations of MgCl₂ and primers, and different temperatures in a Stratagene-Robocycler PCR-machine (all other PCR were done on ABI-480 or ABI-9700). Most intriguing was the variation due to small changes in MgCl₂ concentration. At 2.0 mM a weak nonspecific product of 550 bp became apparent whereas at 2.5 mM and higher this nonspecific product was very prominent in all DNAs including non-template DNA controls. At lower concentrations (less than 1.5 mM) no nonspecific fragments were observed but the expected specific products were very weak. Hybridizations with a <i>BCL1</i>-MTC-internal oligo-probe (5'-ACCGAATATGCAGTGCAGC-3') did not show hybridization to this 550 bp product. PCRs with each of the primers separately revealed that the 550 bp product could be generated by using the J_H-consensus primer only. In some MCL cases, in addition to the PCR-products ranging from 150-350 bp (<figref idref="f0013">Figure 10B</figref>), larger specific PCR-products might be apparent due to annealing of the consensus JH-primer to downstream JH5 and JH6 segments as described for <i>BCL2</i>/JH.¹⁴⁰ From the initial testing phase the most optimal PCR-conditions for the <i>BCL1</i>-MTC/JH-PCR were: annealing temperature of 60°C, 2.0 mM MgCl₂ and 10 pmol of each primer (for 35 PCR-cycles in the ABI 9700).

0177To evaluate the specificity of the PCR on a larger series of cases, the <i>BCL1-</i>MTC/JH-PCR was performed in three laboratories on DNA from in total 25 cases MCL that were all previously identified as positive with in-house <i>BCL1</i>/JH-PCR, and from 18 negative controls. None of the negative cases revealed a PCR-product whereas 22 of 25 positive cases showed products of the expected size. In the three cases that did not reveal a product on agarose-gel, a product was detected with GS suggesting that the sensitivity is lower when compared to in-house PCR.

0178The sensitivity of the PCR was evaluated by amplifying DNA dilutions of a MCL in normal tonsillar DNA. A sensitivity between 10^-3 and 10^-4 was observed on agarose gel using the developed PCR-primers. An in-house PCR performed in parallel on the same samples was at least 10x more sensitive. Hybridizations with the in-house <i>BCL1</i>-MTC-oligo-probe revealed a 10-100x higher sensitivity of both PCRs. Dilutions with DNA of an established cell line JVM2 (available through DSMZ; http://www.dsmz.de) with an <i>BCL1</i>-MTC/JH4-breakpoint⁵³ is used as our standard positive control. As a negative control normal tonsillar tissue or peripheral blood cells might be used, but almost any non-MCL B-cell NHL should be suitable because of the very low frequency of this aberration.¹³⁰

Results of general testing phase

0179To evaluate inter-laboratory variations for the detection of breakpoints at the <i>BCL1</i>-MTC region, ten groups participated in the analysis of DNA from a series of 90 histologically defined malignant and reactive lymphoproliferations using the <i>BCL1-</i>MTC/JH-PCR protocol. All cases were defined for their status at the Ig and TCR loci using Southern hybridization techniques. Of the 90 cases, seven were histologically characterized as MCL. All seven MCL cases were shown to have a clonal <i>IGH</i> rearrangement by Southern hybridization. Assessment of rearrangements within the <i>BCL1</i>-MTC-region at chromosome 11q13 by either Southern hybridization or FISH was not performed in all cases. In six of the seven MCL cases the PCR-product was identified in all ten laboratories. In MCL case NL-15 in six of the laboratories the expected 1.8 kb PCR product was identified. This particular case carries an exceptional breakpoint with an uncommon large PCR-product (normally ranging from 150 to 350 bp) and represents the 3'-most-far detectable <i>BCL1</i>-MTC-breakpoint to our knowledge. In two of six labs the PCR product was observed but initially considered as nonspecific because of its uncommon size. In ES-4, characterized histologically as MCL in none of the ten labs a PCR-product could be detected suggesting that this case carries a breakpoint outside the <i>BCL1</i>-MTC. It should be stressed that the MCL cases submitted to this series for the general testing phase were selected and thus are expected to carry breaks at the <i>BCL1-</i>MTC region at an higher incidence than normal. Importantly, except for one single case (FR-1), in all 83 other non-MCL cases including 16 cases that were histologically characterized as B-CLL, no <i>BCL1-</i> MTC/JH-PCR product was detected in any laboratory. In case FR-1 histologically characterized as B-CLL, in three of the ten labs a product was identified indicating that the number of cells with this break is low. The <i>IGH</i> status determined by Southern blot analysis revealed that this sample was composed of 90% clonal B-cells in good agreement with the histological examination. PCR-based B-cell clonality analyses for <i>IGH</i> and <i>IGK</i> (sensitivity of approximately 1%) revealed a single clone and Southern blot analysis for <i>IGK</i> showed a single major <i>IGK</i> rearrangement only . In addition, Northern blot analysis for expression of cyclin D1 did not show overexpression. All these data suggested that the very small number (less than 1%) t(11;14)-positive cells represent either (i) a subclone derived from the B-CLL, (ii) an independent second B-malignancy or (iii) normal B-cells as described for t(14;18)-positive B-cells in normal individuals.¹⁴⁰ However, with the available data of this patient at present we can not discriminate between these three alternatives. In summary, the analysis by the ten laboratories illustrates the high specificity of the <i>BCL1-</i> MTC/JH-PCR strategy.

0180To evaluate the presence of possible false-negative cases due to the relative low sensitivity of the PCR, in one laboratory the previously described in-house PCR (with about 10-fold higher sensitivity) was performed on DNA of all 90 cases and the PCR products of both assays were also hybridized with an internal-<i>BCL1</i>-MTC oligo-probe that increases the sensitivity another 10-100-fold. This analysis revealed no PCR products in other cases.

Conclusion

0181We conclude that also the sensitivity of the <i>BCL1</i>-MTC/JH PCR (between 10^-3 and 10^-4) is sufficiently high for the detection of the <i>BCL1</i>-MTC/JH-breakpoint in diagnostic material. The results of this approach are very encouraging and suggest that the definition of common approaches and reaction conditions can minimize erroneous results. However, it should be remembered that maximally about 50% of the t(11;14) breakpoints in MCL will be detected and that for diagnosis additional detection tools are recommended.

EXAMPLE 9. t(14;18) with <i>BCL2-IGH</i> rearrangement

Background

0182The t(14;18) is one of the best characterized recurrent cytogenetic abnormalities in peripheral B cell lymphoproliferative disease.¹⁴¹ It is detectable in up to 90% of follicular lymphomas and 20% of large cell B-cell lymphomas depending upon the diagnostic test used.¹⁴² As a consequence of the translocation the BCL2 gene from 18q32 is placed under the control of the strong enhancers of the <i>IGH</i> locus resulting in deregulation of its normal pattern of expression.^{143, 144} BCL2 is located on the outer mitochondrial membrane and its normal function is to antagonize apoptosis and when deregulated it is intimately involved in the pathogenesis of the tumor.^145-148 As a consequence of this role in pathogenesis the t(14;18) provides an ideal target for both diagnosis and molecular monitoring of residual disease.

0183The <i>IGH</i> locus is located at 14q32.3 with the V_H regions lying telomeric and the D_H, J_H and constant regions placed more centromeric. The transcriptional orientation is from telomere to centromere with enhancers located 5' of the V regions and between each of the constant regions. The most common form of the translocation involves the process of VDJ recombination and one of the six germline J_H regions is closely opposed to <i>BCL2.</i> Most PCR based detection strategies have utilized a consensus J_H primer that will detect the majority of translocations. ^{149, 150} In contrast to the <i>IGH</i> locus, the pattern of breaks in <i>BCL2</i> is more complicated. BCL2 is located on chromosome 18q21 and is orientated 5' to 3' from centromere to telomere. The majority of breakpoints fall within the 150 bp MBR located in the 3' untranslated region of exon 3.¹⁵¹ As a consequence of the translocation, the Sµ enhancer located 3' of the J_H regions is placed in close proximity to the BCL2 gene leading to its deregulation. As more translocations have been investigated it has become apparent that there are a number of other breakpoint regions which must be taken into account for an efficient PCR detection strategy. Positioned 4 kb downstream of the MBR is a further breakpoint region, the 3'MBR subcluster, encompassing a region of 3.8 kb.¹⁵² The mcr is located 20 kb 3' of the MBR and covers a region of 500 bp.¹⁵³ However, though analogous to the MBR, the mcr is more extensive than was initially envisaged and a region 10 kb upstream of the mcr, the 5' mcr subcluster, has been described.^{154, 155} In addition to these classical breakpoints a number of variant translocations are described where the breaks occur 5' of <i>BCL2.</i>¹⁵⁶ These are, however, rare and thus can not be taken into account using a PCR based detection strategy.

0184There is no single gold standard detection strategy for the t(14;18) and a combination of cytogenetics and Southern blotting have been generally used.^{157, 158} Interphase FISH detection strategies offer an applicable alternative that have the potential to pick up more translocations.¹⁵⁹ In contrast DNA based fiber FISH has been very informative for defining variant translocations but is unsuitable for routine application.¹⁶⁰ For molecular diagnostic laboratories PCR based detection strategies offer rapid results, are generally applicable and can be used for residual disease monitoring. However, the primers commonly used have been derived on an <i>ad hoc</i> basis and have not been designed to take into account recent information on the molecular anatomy of the breakpoints. As a consequence when compared to gold standard approaches, PCR based techniques only detect up to 60% of translocations which seriously impairs the diagnostic capability of PCR. Compounding this high percentage of false negative results is the problem of false positive results arising from contamination from other samples and previously amplified PCR products.

Primer design

0185We initially evaluated a two tube multiplex system, one tube designed to detect breakpoints within the MBR and a second tube used to identify breakpoints outside this region. The MBR strategy contained three primers MBR1, MBR2 and the consensus J_H primer. The second multiplex reaction contained five primers, MCR1, MCR2, 5'mcr, 3' MBR1 and the consensus JH (<figref idref="f0014">Figure 11A</figref>) and was designed to detect breakpoints within the mcr, 5'mcr and 3' MBR regions.

Results of initial testing phase

0186The evaluation of these primers was performed in three laboratories on DNA derived from a total of 124 cases of follicular lymphoma known to carry a t(14; 18). 109 cases (88%) were identified with an <i>BCL2-IGH</i> fusion, 83/124 (67%) were positive using the MBR multiplex and 26/124 (21%) were positive using the non-MBR multiplex strategy. In 15/124 (12%) cases there was no amplifiable PCR product. Further examination of the cases identified with the non-MBR multiplex showed that 11 (9%) had a breakpoint within the mcr, five cases (4%) within the 5'mcr and 10/124 (8%) within the 3'MBR.

0187To further investigate the value of this set of primers for the detection of breakpoints within the 5'mcr and 3'MBR sub-cluster regions a series of 32 cases of t(14;18) positive follicular lymphomas known to be germline at the MBR and mcr by Southern hybridization were analyzed in one laboratory. Five of the cases had breakpoints within the 5'mcr (260-490bp) and were amplified using both the 5'mcr primer in isolation and with the multiplex reaction. None of the remainder of cases showed a positive result. Of the series of 32 cases, nine were already known to have breakpoints within the 3'MBR region and the multiplex approach was able to detect 5/9 of these cases.

0188In order to improve the sensitivity of the assay within this region we designed three further primers that spanned the 3'MBR sub-cluster region; 3'MBR2, 3'MBR3 and 3'MBR4 and combined them with 3'MBR1 and the consensus JH in an additional multiplex reaction; 3'MBR multiplex (<figref idref="f0014">Figure 11</figref>). This new approach confirmed that eight of the 32 cases were positive but missed the ninth case. The primers were then used individually and in this experiment 11 of the 32 cases were positive. The breakpoints were distributed as follows; 2/11 cases had a breakpoint present between primer 3'MBR1 and 3'MBR2, 3/11 cases between primers 3'MBR2 and 3'MBR3, 2/11 cases between primers 3'MBR3 and 3'MBR4 and the remaining four cases amplified using primer 3'MBR4 and were distributed 200-1000bp 3' of this primer. In this series of cases there were three false negative results using the 3'MBR multiplex. One of the cases was a true false negative where the break occurred in the middle of the 3'MBR, in proximity to an Alu repeat sequence. The translocation was detected using the 3'MBR3 primer when used in isolation and a product of 450 bp was generated suggesting a reduced sensitivity of the multiplex. The remaining two false negative cases generated products larger than 1000bp with the 3'MBR4 primer, placing them in the far 3'MBR not fully covered by this approach. Further improvement in the sensitivity of the 3'MBR assay has been achieved following the general testing phase of this study. Substituting primer 3'MBR3 with a new downstream primer 5'-GGTGACAGAGCAAAACATGAACA-3' (see <figref idref="f0014">Figure 11A</figref>) significantly improved both the sensitivity and specificity of the 3'MBR assay.

0189Based on this, the 3'MBR multiplex was incorporated into our diagnostic strategy. Analysis of the Southern blot defined cases was therefore carried out using the three tube multiplex system presented in <figref idref="f0014">Figure 11A</figref>.

Results of general testing phase

0190Inter-laboratory variations feature significantly in diagnostic PCR strategies. To evaluate this, 11 groups participated in an extensive external quality control exercise. DNA was extracted from a series of 90 histologically defined malignant and reactive lymphoproliferations were analyzed using the t(14;18) multiplex protocol (<figref idref="f0014">Figure 11B</figref>, C, and D). All cases were defined for their status at the Ig and TCR loci using Southern hybridization techniques. Karyotypic confirmation of the t(14;18) was not available on this series. We therefore adopted an approach requiring greater than 70% concordance between members of the network for acceptance of the t(14;18). Of the 90 cases, 11 were characterized histologically as follicular lymphoma. All 11 cases were shown to have a clonal <i>IGH</i> rearrangement by Southern hybridization. Assessment of rearrangements within the <i>BCL2</i> gene was also performed by Southern hybridization using specific probes to the MBR, mcr and 3'MBR in 10/11 cases. 4/10 cases showed a rearrangement within the MBR that was concordant with the PCR result. A single case, GBS-7, shown to be mcr multiplex positive, gave an inconclusive SB result with the mcr probe. Immunophenotypically this case demonstrated two distinct clonal populations, representing approximately 5% and 15% of the original diagnostic material. The discrepancy between the two techniques in this case probably represents the reduced sensitivity of SB compared with PCR. There was no evidence of a 3'MBR rearrangement in any of the remaining cases by SB.

0191Of the six SB negative FCL cases, a single case; ES-7, showed a t(14;18) using the MBR multiplex. 5/11 FCL cases showed no evidence of a t(14;18) by either SB or PCR. A t(14;18) was detected in two further cases by PCR; FR-6, a case of DLBCL showed an MBR breakpoint and was identified by all 11 laboratories, this finding is compatible with previous studies that have detected a t(14; 18) in 20-40% of DLBCL cases.^{161, 162} Using the 3'MBR multiplex, 10/11 laboratories reported a positive result for sample ES-12, this was a case of Hodgkin's disease which contained very few B cells. It is difficult to explain this result in the absence of an <i>IGH</i> rearrangement by Southern blotting. Contamination or incorrect labeling of the sample at source is the most likely explanation.

0192Overall there was excellent concordance throughout the network, although small numbers of both false positive and false negative results were encountered. Overall 12 false positive results were identified, representing less than 0.4% (12/3036) of the total number of analyses. These were reported by five laboratories and involved six of the samples. The majority of the false positives (9/12) were found in three cases. Five false negative results, representing a 6% (5/88) failure rate, were reported by three laboratories, ES-7 was not detected by two laboratories, three further groups within the network commented that this case had shown weak amplification signals with the MBR multiplex. The remaining three false negative cases were reported in isolation by individual laboratories. The results of diagnoses using this approach are very encouraging and suggest that the definition of common approaches and reaction conditions can minimize erroneous results.

Conclusion

0193In conclusion, we have designed and evaluated a robust three-tube multiplex PCR in order to maximize the detection of the t(14;18). This strategy is capable of amplifying across the breakpoint region in the majority of cases of FCL with a cytogenetically defined translocation. Although the sensitivity of this strategy is lower than conventional single round or nested PCR approaches, it is still perfectly acceptable for diagnostic procedures. The widespread adoption of standardized reagents and methodologies has helped to minimize inaccurate results within this large multi-center network. However, it is noteworthy from the general testing phase of this study that it is impossible to detect a t(14;18) in all cases. This is certainly influenced by additional molecular mechanisms capable of deregulating the BCL2 gene. ^{163, 164}

<i>EXAMPLE 10: Use of DNA extracted from paraffin-embedded tissue biopsies and development of control gene primer set</i>

Background

0194Fresh/frozen tissue is considered to be the ideal sample type for extraction of DNA for use in PCR-based clonality analysis. However, fresh/frozen material is not always available to diagnostic laboratories and in many laboratories throughout Europe, paraffin-embedded tissue samples constitute the majority of diagnostic biopsies submitted for analysis. DNA extracted from paraffin-embedded material is often of poor quality and so PCR protocols need to be evaluated for use with these sample types before they can be widely used in diagnostic laboratories.

0195The integrity of DNA extracted from paraffin-embedded samples and its amplification by PCR are affected by a number of factors such as thickness of tissue, fixative type, fixative time, length of storage before analysis, DNA extraction procedures and the co-extraction of PCR inhibitors.^165-172 Ten percent neutral buffered formalin (10% NBF) is the most commonly used fixative, although laboratories also use a number of other fixatives, including unbuffered formalin and Bouins. The use of 10% NBF permits the amplification of DNA fragments of a wide range of sizes whereas Bouins appears to be the least amenable for use in PCR analysis.^{167, 168, 171, 173} The integrity of DNA fragments extracted from paraffin-embedded samples also depends on the length of time the blocks have been stored with the best results usually obtained from blocks less than 2 years old, while blocks over 15 years old tend to yield very degraded fragments.¹⁷⁴

Primer design

0196Initially, five pairs of control gene PCR primers were designed to amplify products of exactly 100, 200, 400, 600 and 1,000 bp in order to assess the quality of DNA submitted for analysis. The target genes were selected on the basis of having large exons with open reading frames to reduce the risk of selecting polymorphic regions and the primers were designed for multiplex usage in the standardized protocols. The following target genes were selected: human thromboxane synthase gene (<i>TBXAS1,</i> Exon 9; GenBank Accession No D34621), human recombination activating gene (<i>RAG1,</i> Exon 2; GenBank Accession No M29474), human promyelocytic leukemia zinc finger gene (<i>PLZF</i>, Exon 1; GenBank Accession No AF060568), and human AF4 gene (Exon 3; GenBank Accession No Z83679, and Exon 11; GenBank Accession No Z83687).

Results of initial testing phase

0197The primer pairs were tested in separate reactions and subsequently in multiple reactions using high molecular weight DNA. Due to the large size range of the products (100 to 1,000 bp), it was necessary to vary the ratio of primer concentrations to obtain bands of equal intensities in the multiplex reactions. However, it proved extremely difficult to be able to amplify all the bands reproducibly and it was decided that the 1,000 bp product was probably unnecessary, since all the PCR protocols give products of less than 600 bp. It was therefore decided to exclude the 1,000 bp product in order to improve the reproducibility of the assay. By increasing the MgCl₂ concentration to 2 mM and adding the primers in a 1:1:1:2 ratio, it was possible to reproducibly amplify four bands (100, 200, 400 and 600 bp) of equal intensity from high molecular weight DNA samples. However, for DNA extracted from paraffin blocks, it was thought that an extra size marker at 300 bp would be extremely informative and that the 600 bp marker might not be necessary. Using the gene sequence for the 1,000 bp marker (<i>PLZF</i>), primers were redesigned to generate a 300 bp product. These were tested successfully both in monoplex reactions and in multiplex reactions combining the 100, 200, 300, 400 and 600 bp primers (see <figref idref="f0015">Figure 12A</figref>).

0198Thus two primer sets are available for assessing the quality of DNA for amplification: The 100, 200, 300 and 400 bp primers used at 2.5 pmol each can be used for assessing DNA from paraffin-embedded tissues. The addition of the 600 bp primers at 5 pmol allows this set to be used to check the quality of any DNA sample for use with the disclosed primers and protocols. Both primer sets can be used with ABI Buffer II and 2.0 mM MgCl₂ under standardized amplification conditions. Products can be analyzed on 6% PAGE or 2% agarose (see <figref idref="f0015">Figure 12B</figref>).

Results of general testing phase

0199Forty five paraffin-embedded biopsies were collected corresponding to 30 of the B-cell malignancies, eight of the T-cell malignancies and seven of the reactive lymphoproliferations submitted as fresh/frozen tissue samples. The age of the paraffin blocks as well as the methods of fixation and embedding of the samples varied between National Networks. The ES samples were submitted as pre-cut sections, NL-14, 15 and 16 were submitted as DNA samples and the remaining biopsies were submitted as paraffin blocks. Five sections (10 pm each) were cut from the paraffin blocks and DNA was extracted using the QIAamp DNA Mini Kit (QIAGEN) following the manufacturer's protocol for isolation of genomic DNA from paraffin-embedded tissue. This method of

0200DNA extraction was chosen since the kit can be used to rapidly extract good quality DNA from blood, fresh/frozen tissue and paraffin-embedded tissue and thus enables the parallel processing of a variety of sample types with assured quality control. Numerous protocols for extraction of DNA from paraffin-embedded tissue for PCR analysis have been published. ^{171, 172, 175-177} Many of these aim to reduce DNA degradation and co-extraction of PCR inhibitors, but many of these methods require prolonged extraction procedures and can be unsuitable for use in the routine diagnostic laboratory. ^{166, 178, 179}

0201DNA sample concentration and integrity were estimated by spectrophotometry and by comparison of sample DNA with known standards on agarose gel electrophoresis. DNA samples (100 ng) were then analyzed for integrity and amplifiability using the control gene PCR primers (100-400 bp) and assessed for clonality at all target loci using the PCR protocols.

0202In the control gene PCR reaction of 24/45 cases the amplified products were at least 300 bp, whereas in the remaining 21 samples the amplified products were 200 bp or less. No clear correlation between the quality of the DNA and the age of the block or fixation method could be demonstrated. Therefore it is likely that a combination of factors is responsible for the DNA quality in these samples.

0203The DNA samples were evaluated for clonality using the 18 multiplex PCR reactions and were analyzed by both HD and GS. The number of paraffin samples showing clonality and translocations at the nine target loci were compared with the corresponding fresh/frozen sample data. In samples with control gene PCR products of up to 200 bp, the overall detection of clonality at the nine target loci was 9/55 (16%). Of the 46 missed rearrangements, 45 could be explained by the fact that the expected clonal PCR products had a molecular weight higher than the maximum size amplified by the sample in the control gene PCR. The remaining sample (PT-9) amplified to 100 bp in the control gene PCR but the expected 81 bp <i>TCRG</i> clonal product was not detected. In samples with control gene PCR products of at least 300 bp, the overall detection of clonality at the nine target loci was 42/55 (76%). Of the 13 missed rearrangements, five could again be explained by the fact that the expected clonal PCR products were larger than the maximum size amplified by the sample in the control gene PCR. The remaining eight missed rearrangements could not be explained directly by the quality of the DNA. One false positive clonal result (GBN-9; <i>IGL</i>) was detected in a reactive lymph node which may represent pseudoclonality.

0204PCR inhibitors are known to be present in DNA extracted from paraffin samples. Dilution of the DNA sample may reduce the concentration of these inhibitors to levels that allow successful amplification to occur. To investigate the effect of diluting DNA samples on the efficiency of amplification, four different concentrations of DNA were tested in the control gene PCR reaction: 5, 50, 100 and 500 ng. We observed that dilution of the DNA samples has a significant effect on the size of the PCR products in the control gene PCR. Overall, 24/45 cases (53%) showed an increased efficiency of amplification when diluted from 100 ng to 50 ng. The optimal DNA concentration appears to be between 50 to 100 ng whereas the use of 500 ng appears to inhibit the amplification of large products (300 bp or above). Although the use of 5 ng of DNA gives acceptable results with the control gene PCR, this can lead to false positivity in PCR-based clonality assays due to the low representation of total lymphoid cell DNA. ^{160, 161} More importantly, 5 ng of DNA has no advantage over a dilution to 50 ng of DNA.

0205To assess whether the use of 50 ng of DNA would also increase the detection of clonality, all the samples were retested at the <i>IGH</i> V-J locus using this DNA concentration. The number of clonal rearrangements detected in the three <i>IGH</i> V-J tubes using 100 ng of DNA was 12, compared with 23 using the corresponding fresh/frozen samples. The overall detection of clonality at this locus increased to 17 out of 23 when 50 ng of DNA was used, with an additional 9 FR1, 6 FR2 and 4 FR3 clonal products being detected. Thus dilution of the DNA can increase the detection of clonal products, presumably because of dilution of PCR inhibitors. Logically, dilution of DNA is only likely to improve both control gene PCR results and the detection of clonality, if PCR inhibitors are present, not if the DNA sample is highly degraded. Therefore it is recommended that at least two dilutions of DNA are tested using the control gene PCR and that the dilution that gives the better result is used in subsequent clonality analysis.

0206Nine clonal rearrangements remained undetected after initial analysis, which could not be explained by DNA quality (<i>TCRG</i> in PT-9 and NL-11; <i>TCRB</i> in GBS-4; <i>TCRD</i> in NL-15; <i>IGK</i> in GBN-4, NL-4 and NL-5; <i>IGH</i> V-J_H in GBS-6 and GBS-8). These samples were retested using 50 ng of DNA, but only one sample (GBS8; <i>IGH</i>) showed improved detection, suggesting that other, unknown, factors can prevent amplification of specific targets in a small number of cases. However, it should be noted that for seven of these samples (NL-11, GBS-4, NL-15, GBN-4, NL-5, GBS-6 &amp; GBS-8) clonal products were detected in at least one other locus. This demonstrates that testing for clonality at multiple target loci increases the likelihood of detecting clonal lymphocyte populations.

Conclusion

0207In conclusion, the protocols as provided herein work well with DNA extracted from paraffin-embedded material provided that the DNA can amplify products of 300 bp or more in the control gene PCR. Two concentrations of DNA are preferably tested in the control gene PCR and the more 'amplifiable' concentration should be used in further testing, although with the proviso that concentrations of DNA less than 20 ng may contribute to the detection of pseudoclonality due to the low representation of target lymphoid DNA. ^{180, 181} Overall the data show that assessment of DNA quality using the control gene PCR provides a good indication of the suitability of the DNA for clonality analysis using the protocols provided. It is also important to note that the control gene PCR will give no indication of the amount of lymphoid cell DNA present in the sample and therefore good quality DNA may still produce negative results for clonality analysis. To ensure monoclonal results are reproducible (and to avoid potential pseudoclonality), all clonality assays, particularly using paraffin-extracted DNA, are preferably performed in duplicate and analyzed by HD and GS, wherever possible.

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Mol Pathol 1999; 52: 104-110</text></nplcit>.</entry></row></tbody></tgroup></table></tables><tables id="tabl0004" num="0004"><table frame="topbot"><title><b>Table 1. B, T, and NK lineage of lymphoid malignancies^a</b></title><tgroup cols="8" colsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="18mm" /><colspec colnum="4" colname="col4" colwidth="31mm" /><colspec colnum="5" colname="col5" colwidth="17mm" /><colspec colnum="6" colname="col6" colwidth="20mm" /><colspec colnum="7" colname="col7" colwidth="17mm" /><colspec colnum="8" colname="col8" colwidth="31mm" /><thead><row><entry morerows="1" valign="top">Lineage</entry><entry namest="col2" nameend="col3" align="center" valign="top">ALL</entry><entry morerows="1" valign="top">Chronic lymphocytic leukemias</entry><entry namest="col5" nameend="col7" align="left" valign="top">Non-Hodgkin lymphomas</entry><entry morerows="1" valign="top">Multiple myeloma</entry></row><row><entry valign="top">childhood</entry><entry valign="top">adult</entry><entry valign="top">nodal</entry><entry valign="top">extranodal</entry><entry valign="top">skin</entry></row></thead><tbody><row rowsep="0"><entry>B</entry><entry align="right">82 - 86%</entry><entry align="right">75 - 80%</entry><entry align="right">95 - 97%</entry><entry align="right">95 - 97%</entry><entry align="right">90 - 95%</entry><entry align="right">30 - 40%</entry><entry align="right">100%</entry></row><row rowsep="0"><entry>T</entry><entry align="right">14 - 18%</entry><entry align="right">20 - 25%</entry><entry align="right">3 - 5%</entry><entry align="right">3 - 5%</entry><entry align="right">5 - 10%</entry><entry align="right">60 - 70%</entry><entry align="right">0%</entry></row><row><entry>NK</entry><entry align="right">< 1%</entry><entry align="right">< 1%</entry><entry align="right">1 - 2%</entry><entry align="right">< 2%</entry><entry align="right">< 2%</entry><entry align="right">< 2%</entry><entry align="right">0%</entry></row></tbody></tgroup><tgroup cols="8" rowsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="18mm" /><colspec colnum="4" colname="col4" colwidth="31mm" /><colspec colnum="5" colname="col5" colwidth="17mm" /><colspec colnum="6" colname="col6" colwidth="20mm" /><colspec colnum="7" colname="col7" colwidth="17mm" /><colspec colnum="8" colname="col8" colwidth="31mm" /><tbody><row><entry namest="col1" nameend="col8" align="justify">a. See Van Dongen et al. 1991 ¹, Jaffe et al. 2001 ², and Van Dongen et al. 2002 ⁵</entry></row></tbody></tgroup></table></tables><tables id="tabl0005" num="0005"><table frame="topbot"><title><b>Table 2. Estimated number of non-polymorphic human V, D, and J gene segments that can potentially be involved in Ig or TCR gene rearrangements^a</b></title><tgroup cols="8" colsep="0"><colspec colnum="1" colname="col1" colwidth="25mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><colspec colnum="6" colname="col6" colwidth="21mm" /><colspec colnum="7" colname="col7" colwidth="21mm" /><colspec colnum="8" colname="col8" colwidth="21mm" /><thead><row><entry valign="top">Gene segment</entry><entry valign="top"><i>IGH</i></entry><entry valign="top"><i>IGK</i></entry><entry valign="top"><i>IGL</i></entry><entry valign="top"><i>TCRA</i></entry><entry valign="top"><i>TCRB</i></entry><entry valign="top"><i>TCRG</i></entry><entry valign="top"><i>TCRD</i></entry></row><row rowsep="0"><entry valign="top">V segments</entry><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /></row></thead><tbody><row rowsep="0"><entry>- functional</entry><entry>44 (7)</entry><entry>43 (7)</entry><entry>38 (10)</entry><entry>46 (32)</entry><entry>47 (23)</entry><entry>6 (4)</entry><entry>8</entry></row><row rowsep="0"><entry>(family)</entry><entry>66 (7)^b</entry><entry>76 (7)</entry><entry>56 (11)</entry><entry>54 (32)</entry><entry>67 (30)</entry><entry>9 (4)</entry><entry>8</entry></row><row><entry>- rearrangeable (family)</entry><entry /><entry /><entry /><entry /><entry /><entry /><entry /></row></tbody></tgroup><tgroup cols="8" colsep="0"><colspec colnum="1" colname="col1" colwidth="25mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><colspec colnum="6" colname="col6" colwidth="21mm" /><colspec colnum="7" colname="col7" colwidth="21mm" /><colspec colnum="8" colname="col8" colwidth="21mm" /><thead><row rowsep="0"><entry valign="top">D segments</entry><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /></row></thead><tbody><row><entry>- rearrangeable (family)</entry><entry>27(7)</entry><entry>-</entry><entry>-</entry><entry>-</entry><entry>2</entry><entry>-</entry><entry>3</entry></row></tbody></tgroup><tgroup cols="8" colsep="0"><colspec colnum="1" colname="col1" colwidth="25mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><colspec colnum="6" colname="col6" colwidth="21mm" /><colspec colnum="7" colname="col7" colwidth="21mm" /><colspec colnum="8" colname="col8" colwidth="21mm" /><thead><row rowsep="0"><entry valign="top">J segments</entry><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /><entry valign="top" /></row></thead><tbody><row rowsep="0"><entry>- functional</entry><entry>6^c</entry><entry>5^d</entry><entry>4</entry><entry>53</entry><entry>13</entry><entry>5</entry><entry>4</entry></row><row><entry>- rearrangeable</entry><entry>6^c</entry><entry>5^d</entry><entry>5^e</entry><entry>61</entry><entry>13</entry><entry>5</entry><entry>4</entry></row></tbody></tgroup><tgroup cols="8" rowsep="0"><colspec colnum="1" colname="col1" colwidth="25mm" /><colspec colnum="2" colname="col2" colwidth="19mm" /><colspec colnum="3" colname="col3" colwidth="21mm" /><colspec colnum="4" colname="col4" colwidth="20mm" /><colspec colnum="5" colname="col5" colwidth="21mm" /><colspec colnum="6" colname="col6" colwidth="21mm" /><colspec colnum="7" colname="col7" colwidth="21mm" /><colspec colnum="8" colname="col8" colwidth="21mm" /><tbody><row><entry namest="col1" nameend="col8" align="justify">a. Only non-polymorphic gene segments with a suitable RSS are included in this table. b. This estimation does not include the recently discovered (generally truncated) VH pseudogenes, which are clustered in three clans c. The six J_H gene segments are highly homologous over a stretch of ∼20 nucleotides, which is sufficient for the design of a consensus primer. d. The Jκ segments have a high homology, which allows the design of 2 to 3 Jκ consensus primers. e. Five of the seven Jλ gene segments have a suitable RSS.</entry></row></tbody></tgroup></table></tables><tables id="tabl0006" num="0006"><table frame="topbot"><title><b>Table 3. Standardized PCR protocol</b></title><tgroup cols="4" colsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="30mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><colspec colnum="4" colname="col4" colwidth="28mm" colsep="1" /><thead><row rowsep="0"><entry namest="col1" nameend="col4" align="left" valign="top"><i>Reaction conditions.</i></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• buffer: ABI Buffer II or ABI Gold Buffer</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• 50 µl final volume</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• 100 ng DNA</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• 10 pmol of each primer (unlabeled or 6-FAM labeled)</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">(irrespective of total numbers of primers in each multiplex PCR tube)</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• dNTP: 200 µM final concentration</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• MgCl₂: 1.5 mM final concentration (to be optimized per target)</entry></row><row><entry namest="col1" nameend="col4" align="left">• <i>Taq</i> enzyme^a: 1U in most tubes; 2U in tubes with many primers (>15)</entry></row></tbody></tgroup><tgroup cols="4" colsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="30mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><colspec colnum="4" colname="col4" colwidth="28mm" colsep="1" /><thead><row rowsep="0"><entry namest="col1" nameend="col4" align="left" valign="top"><i>Cycling conditions</i></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• pre-activation 7 min. at 95°C</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• annealing temperature: 60°C</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">• cycling times:</entry><entry>"classical"</entry><entry>"newer"</entry></row><row><entry rowsep="0" /><entry rowsep="0" /><entry><i>PCR equipment</i></entry><entry><i>PCR equipment</i></entry></row><row rowsep="0"><entry /><entry>-denaturation</entry><entry>45 sec.</entry><entry>30 sec.</entry></row><row rowsep="0"><entry /><entry>-annealing</entry><entry>≥45 sec.</entry><entry>≥30 sec.</entry></row><row rowsep="0"><entry /><entry>-extension</entry><entry>1.30 min.</entry><entry>≥30 sec.</entry></row><row rowsep="0"><entry /><entry>-final extension</entry><entry>≥10 min.</entry><entry>≥10 min.</entry></row><row rowsep="0"><entry namest="col1" nameend="col4" align="left">• number of cycles: 35</entry></row><row><entry namest="col1" nameend="col4" align="left">• hold 15°C (or room temperature)</entry></row></tbody></tgroup><tgroup cols="4" rowsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="30mm" /><colspec colnum="3" colname="col3" colwidth="28mm" /><colspec colnum="4" colname="col4" colwidth="28mm" /><tbody><row><entry namest="col1" nameend="col4" align="justify">a. Ampli<i>Taq</i> Gold (Applied Biosystems, Foster City, CA) was used in combination with 1x ABI Buffer II or 1x ABI Gold Buffer (Applied Biosystems), depending on the target.</entry></row></tbody></tgroup></table></tables><tables id="tabl0007" num="0007"><table frame="topbot"><title><b>Table 4. Standardized protocol for heteroduplex analysis of PCR products</b></title><tgroup cols="1" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="165mm" /><thead><row><entry valign="top"><i>PCR product preparation</i></entry></row></thead><tbody><row><entry>• tube with 10-20 µl of PCR product</entry></row><row><entry>• denaturation of PCR product: 5 min. at 95°C</entry></row><row><entry>• re-annealing of PCR product: 60 min. at 4°C</entry></row><row rowsep="1"><entry /></row></tbody></tgroup><tgroup cols="1" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="165mm" /><thead><row><entry valign="top"><b><i>Electrophoresis conditions (non-commercial polyacrylamide gels)</i></b></entry></row></thead><tbody><row><entry>• gel: 6% non-denaturing polyacrylamide (acrylamide: bisacrylamide 29: 1)</entry></row><row><entry>• buffer: 0.5 x TBE</entry></row><row><entry>• loading buffer: 5 µl ice-cold non-denaturing bromophenol blue loading buffer</entry></row><row><entry>• electrophoresis: typically 2-3 hours at 110 V or overnight at 40-50 V^a</entry></row><row rowsep="1"><entry /></row></tbody></tgroup><tgroup cols="1" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="165mm" /><thead><row><entry valign="top"><i>Electrophoresis conditions (commercial polyacrylamide gels)</i></entry></row></thead><tbody><row><entry>• gel: non-denaturing polyacrylamide (e.g. BioRad PreCast Gel System or Amersham Pharmacia Biotech Gene Gel Excel Kit)</entry></row><row><entry>• buffer: 1 x TBE</entry></row><row><entry>• loading buffer: ice-cold non-denaturing bromophenol blue loading buffer</entry></row><row><entry>• electrophoresis: 1,5 hours at 100 V</entry></row><row rowsep="1"><entry /></row></tbody></tgroup><tgroup cols="1" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="165mm" /><thead><row><entry valign="top"><i>Visualization</i></entry></row></thead><tbody><row><entry>• staining: 5-10 min. in 0.5 µg/ml EtBr in H₂O</entry></row><row><entry>• destaining / washing: 2x 5-10 min. in H₂O</entry></row><row><entry>• visualization: UV illumination</entry></row><row rowsep="1"><entry>• alternative: silver staining using Amersham Pharmacia Biotech DNA Silver stain kit</entry></row></tbody></tgroup><tgroup cols="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="165mm" /><tbody><row><entry align="justify">a. Voltage and electrophoresis time depend on PCR amplicon sizes, thickness of polyacrylamide gel, and type of PCR equipment, and should be adapted accordingly.</entry></row></tbody></tgroup></table></tables><tables id="tabl0008" num="0008"><table frame="topbot"><title><b>Table 5. Standardized protocol for GeneScanning of PCR products</b></title><tgroup cols="2" colsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><thead><row rowsep="0"><entry namest="col1" nameend="col2" align="left" valign="top"><b>A. Gel-based sequencers</b></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col2" align="left" /></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left"><i>PCR product preparation</i></entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">1. PCR product dilution: initially 1: 10 in formamide or H₂O (can be altered if fluorescent signal is outside optimal range; see electrophoresis conditions)</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">2. sample volume: 2 µl diluted PCR product</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">3. loading buffer volume: 0.5 µl blue dextran loading buffer + 0.5 µl TAMRA internal standard + 2 µl deionized formamide</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">4. denaturation of PCR product: 2 min. at 95°C or higher temperature</entry></row><row><entry namest="col1" nameend="col2" align="left">5. cooling of PCR product at 4°C</entry></row></tbody></tgroup><tgroup cols="2" colsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><thead><row rowsep="0"><entry namest="col1" nameend="col2" align="left" valign="top"><i>Electrophoresis conditions</i></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col2" align="left">6. gel: 5% denaturing polyacrylamide</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">7. buffer: 1 x TBE</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">8. electrophoresis: 2-3.5 hours^a (see Table 25)</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">9. optimal fluorescent signal intensity:</entry></row><row rowsep="0"><entry /><entry>- 600-4,000 fluorescent units (373 platforms)</entry></row><row rowsep="0"><entry /><entry>- 400-7,000 fluorescent units (377 platforms)</entry></row><row><entry namest="col1" nameend="col2" align="left" /></row></tbody></tgroup><tgroup cols="2" colsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><thead><row rowsep="0"><entry namest="col1" nameend="col2" align="left" valign="top"><b>B. Capillary sequencers (to be optimized per sequencer)</b></entry></row></thead><tbody><row><entry namest="col1" nameend="col2" align="left" /></row></tbody></tgroup><tgroup cols="2" colsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><thead><row rowsep="0"><entry namest="col1" nameend="col2" align="left" valign="top"><i>PCR product preparation</i></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col2" align="left">1. 1 µl PCR product (volume of PCR product or sampling times can be altered if fluorescent signal is outside optimal range; see electrophoresis conditions)</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">2. sample volume: 1 µl PCR product + 9.5 µl (Hi-Di) formamide + 0.5 µl ROX-400 heteroduplex analysis internal standard</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">3. denaturation of PCR product: 2 min. at 95°C or higher temperature</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">4. cooling of PCR product at 4°C for an hour</entry></row><row><entry namest="col1" nameend="col2" align="left" /></row></tbody></tgroup><tgroup cols="2" colsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><thead><row rowsep="0"><entry namest="col1" nameend="col2" align="left" valign="top"><i>Electrophoresis conditions</i></entry></row></thead><tbody><row rowsep="0"><entry namest="col1" nameend="col2" align="left">5. gel: 3100 POP4 polymer</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">6. buffer: 1x 3100 buffer with EDTA</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">7. electrophoresis: 45 minutes^e</entry></row><row rowsep="0"><entry namest="col1" nameend="col2" align="left">8. optimal fluorescent signal intensity:</entry></row><row><entry /><entry>- up to 10,000 fluorescent units</entry></row></tbody></tgroup><tgroup cols="2" rowsep="0"><colspec colnum="1" colname="col1" colwidth="83mm" /><colspec colnum="2" colname="col2" colwidth="83mm" /><tbody><row><entry namest="col1" nameend="col2" align="justify">^a Electrophoresis time depends on amplicon sizes and on employed platform. ^b For 36 cm capillary; time taken depends on capillary used.</entry></row></tbody></tgroup></table></tables><tables id="tabl0009" num="0009"><table frame="topbot"><title><b>Table 6. Sensitivity of detection of clonal TCRB rearrangements</b></title><tgroup cols="7" colsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="27mm" /><colspec colnum="5" colname="col5" colwidth="26mm" /><colspec colnum="6" colname="col6" colwidth="23mm" /><colspec colnum="7" colname="col7" colwidth="27mm" colsep="1" /><thead><row><entry morerows="1" valign="top"><b><i>TCRB</i> tube</b></entry><entry namest="col2" nameend="col3" align="center"><b>Involved primer pair</b></entry><entry morerows="1" align="center"><b>Clonal Control</b></entry><entry morerows="1" align="center"><b>Size of PCR product</b></entry><entry namest="col6" nameend="col7" align="center"><b>Sensitivity of detection</b></entry></row><row><entry><b>V</b></entry><entry><b>J</b></entry><entry><b>single PCR^a</b></entry><entry><b>multiplex PCR</b></entry></row></thead><tbody><row rowsep="0"><entry valign="bottom"><b>tube A</b></entry><entry valign="bottom">Vβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.2</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">261 nt</entry><entry align="center" valign="bottom">1-5%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.3</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">267 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.6</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">267 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ7</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.2</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">254 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ8a</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.2</entry><entry valign="bottom">Jurkat</entry><entry align="center" valign="bottom">267 nt</entry><entry align="center" valign="bottom">0.1%</entry><entry align="center" valign="bottom">0.5 - 1 %</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ8a</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.7</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">264 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ10</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.7</entry><entry valign="bottom">PEER</entry><entry align="center" valign="bottom">263 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">20%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ3/12a/13a/1 5</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.6</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">278 nt</entry><entry align="center" valign="bottom"><5%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ3/12a/13a/1 5</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.7</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">286 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ17</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.7</entry><entry valign="bottom">RPMI-8402</entry><entry align="center" valign="bottom">260 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ17</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">260 nt</entry><entry align="center" valign="bottom">1%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ18</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.2</entry><entry valign="bottom">DND41</entry><entry align="center" valign="bottom">261 nt</entry><entry align="center" valign="bottom">1%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ22</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">265 nt</entry><entry align="center" valign="bottom">0.1%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ8b/23</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.2</entry><entry valign="bottom">H9</entry><entry align="center" valign="bottom">257 nt</entry><entry align="center" valign="bottom">0.1%</entry><entry align="center" valign="bottom">0.5%</entry></row><row><entry valign="bottom" /><entry valign="bottom">Vβ24</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.5</entry><entry valign="bottom">RPMI-8402</entry><entry align="center" valign="bottom">264 nt</entry><entry align="center" valign="bottom">0.5%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom"><b>tube B</b></entry><entry valign="bottom">Vβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">Molt-4</entry><entry align="center" valign="bottom">267 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ1/5</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">266 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">1-5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ6a/11</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">265 nt</entry><entry align="center" valign="bottom">1%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ6a/11</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.5</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">258 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ7</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.3</entry><entry valign="bottom">PEER</entry><entry align="center" valign="bottom">271 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ8a</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">293 nt</entry><entry align="center" valign="bottom">0.1%</entry><entry align="center" valign="bottom">1%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ3/12a/13a/1 5</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">258 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ3/12a/13a/1 5</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.3</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">258 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ16</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">258 nt</entry><entry align="center" valign="bottom">0.5%</entry><entry align="center" valign="bottom">10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Vβ17</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.5</entry><entry valign="bottom">CML-T1</entry><entry align="center" valign="bottom">270 nt</entry><entry align="center" valign="bottom">0.1 - 1%</entry><entry align="center" valign="bottom">1%</entry></row><row><entry valign="bottom" /><entry valign="bottom">Vβ21</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.3</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">282 nt</entry><entry align="center" valign="bottom">0.5%</entry><entry align="center" valign="bottom">< 10%</entry></row><row rowsep="0"><entry valign="bottom"><b>tube C</b></entry><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">304 nt</entry><entry align="center" valign="bottom">0.10%</entry><entry align="center" valign="bottom"><5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.2</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">306 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.4</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">310 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">5-10%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.6</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">320 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">20%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">309 nt</entry><entry align="center" valign="bottom">5%</entry><entry align="center" valign="bottom">20%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.7</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">307 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><5%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ1</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.5</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">310 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><1%</entry></row><row rowsep="0"><entry valign="bottom" /><entry valign="bottom">Dβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ1.4</entry><entry valign="bottom">patient</entry><entry align="center" valign="bottom">182 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom"><1%</entry></row><row><entry rowsep="0" valign="bottom" /><entry rowsep="0" valign="bottom">Dβ2</entry><entry rowsep="0" valign="bottom" align="char" char="." charoff="34">Jβ2.1</entry><entry rowsep="0" valign="bottom">patient</entry><entry rowsep="0" align="center" valign="bottom">185 nt</entry><entry rowsep="0" align="center" valign="bottom">1%</entry><entry rowsep="0" align="center" valign="bottom"><5%</entry></row><row><entry valign="bottom" /><entry valign="bottom">Dβ2</entry><entry valign="bottom" align="char" char="." charoff="34">Jβ2.5</entry><entry align="center" valign="bottom">patient</entry><entry align="center" valign="bottom">191 nt</entry><entry align="center" valign="bottom" /><entry align="center" valign="bottom">5%</entry></row></tbody></tgroup><tgroup cols="7" rowsep="0"><colspec colnum="1" colname="col1" colwidth="21mm" /><colspec colnum="2" colname="col2" colwidth="28mm" /><colspec colnum="3" colname="col3" colwidth="16mm" /><colspec colnum="4" colname="col4" colwidth="27mm" /><colspec colnum="5" colname="col5" colwidth="26mm" /><colspec colnum="6" colname="col6" colwidth="23mm" /><colspec colnum="7" colname="col7" colwidth="27mm" /><tbody><row><entry namest="col1" nameend="col7" align="justify"><i>a. The dilution experiment for assessing the sensitivity of the single PCR was not performed in each case.</i></entry></row></tbody></tgroup></table></tables><tables id="tabl0010" num="0010"><table frame="topbot"><title><b>Table 7. Sensitivity of detection of clonal <i>TCRD</i> gene rearrangements</b></title><tgroup cols="4" colsep="0"><colspec colnum="1" colname="col1" colwidth="38mm" /><colspec colnum="2" colname="col2" colwidth="22mm" /><colspec colnum="3" colname="col3" colwidth="22mm" /><colspec colnum="4" colname="col4" colwidth="65mm" /><thead><row><entry valign="top"><b><i>TCRD</i> rearrangement</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Clonal control sample</b><b>(approximate size)</b></entry><entry valign="top"><b>Sensitivity of detection by heteroduplex</b></entry></row></thead><tbody><row rowsep="0"><entry>Vδ1-Jδ1</entry><entry>patient</entry><entry>(200 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(190 nt)</entry><entry>1-5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(200 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry>Vδ2-Jδ1</entry><entry>patient</entry><entry>(200 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(220 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(210 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry>Vδ2-Jδ3</entry><entry>patient</entry><entry>(220 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry>Vδ3-Jδ1</entry><entry>patient</entry><entry>(270 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry>Vδ6-Jδ2</entry><entry>Loucy</entry><entry>(210 nt)</entry><entry>0.5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(210 nt)</entry><entry>10 %</entry></row><row rowsep="0"><entry>Dδ2-Jδ1</entry><entry>Loucy</entry><entry>(150 nt)</entry><entry>0.2%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(160 nt)</entry><entry>0.5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(135 nt)</entry><entry>0.5%</entry></row><row rowsep="0"><entry>Dδ2-Jδ3</entry><entry>patient</entry><entry>(150 nt)</entry><entry>5%</entry></row><row rowsep="0"><entry>Dδ2-Dδ3</entry><entry>NALM-16</entry><entry>(170 nt)</entry><entry>1%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(200 nt)</entry><entry>1%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(190 nt)</entry><entry>0.5%</entry></row><row rowsep="0"><entry /><entry>patient</entry><entry>(170 nt)</entry><entry>0.5%</entry></row><row rowsep="0"><entry>Vδ2-Dδ3</entry><entry>REH</entry><entry>(240 nt)</entry><entry>5-10%</entry></row><row rowsep="0"><entry /><entry>NALM-16</entry><entry>(230 nt)</entry><entry>1-5%</entry></row><row><entry /><entry>patient</entry><entry>(250 nt)</entry><entry>5%</entry></row></tbody></tgroup></table></tables><tables id="tabl0011" num="0011"><table frame="all"><title><b>Table 8. Concordance between multiplex PCR results and Southern blot (SB) analysis results (PCR/SB) on Ig/TCR gene rearrangements per (sub)category of included frozen samples</b></title><tgroup cols="7"><colspec colnum="1" colname="col1" colwidth="26mm" /><colspec colnum="2" colname="col2" colwidth="24mm" /><colspec colnum="3" colname="col3" colwidth="23mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="23mm" /><colspec colnum="6" colname="col6" colwidth="25mm" /><colspec colnum="7" colname="col7" colwidth="25mm" /><thead><row><entry valign="top"><b>Diagnosis</b></entry><entry valign="top"><b><i>IGH^a</i></b></entry><entry valign="top"><b><i>IGK</i></b></entry><entry valign="top"><b><i>IGL</i></b></entry><entry valign="top"><b><i>TCRB</i></b></entry><entry valign="top"><b><i>TCRG</i></b></entry><entry valign="top"><b><i>TCRD</i></b></entry></row></thead><tbody><row rowsep="0"><entry morerows="1">pre-follicular (n=8)</entry><entry>C^b: 8/8</entry><entry>C: 8/8</entry><entry>C: 4/4</entry><entry>C: 2/4^b</entry><entry>C: 0/0</entry><entry>C: 0/0</entry></row><row><entry>P^b: 0/0</entry><entry>P: 0/0</entry><entry>P: 4/4</entry><entry>P: 4/4</entry><entry>P: 8/8</entry><entry>P: 8/8^e</entry></row><row rowsep="0"><entry morerows="1">B-CLL (n=16)</entry><entry>C:</entry><entry>C: 16/16</entry><entry>C: 5/5</entry><entry>C: 1/1</entry><entry>C: 0/0</entry><entry>C: 2/2</entry></row><row rowsep="0"><entry>15/16</entry><entry>P: 0/0</entry><entry>P: 9/11</entry><entry>P: 15/15</entry><entry>P:</entry><entry>P:</entry></row><row><entry /><entry>P: 0/0</entry><entry /><entry /><entry /><entry>16/16</entry><entry>14/14</entry></row><row rowsep="0"><entry morerows="1">(post-)follicular (n=25)</entry><entry>C:</entry><entry>C:</entry><entry>C: 3/5</entry><entry>C: 2/4</entry><entry>C: 0/1</entry><entry>C: 0/0</entry></row><row rowsep="0"><entry>22/25^b</entry><entry>19/24^c</entry><entry>P:</entry><entry>P:</entry><entry>P:</entry><entry>P:</entry></row><row><entry /><entry>P: 0/0</entry><entry>P: 0/1</entry><entry>19/20</entry><entry>21/21^d,e</entry><entry>22/24</entry><entry>24/25^e</entry></row><row rowsep="0"><entry morerows="2">All B-cell malignancies (n=49)</entry><entry>C:</entry><entry>C:</entry><entry>C:</entry><entry>C: 4/8</entry><entry>C: 0/1</entry><entry>C: 2/2</entry></row><row rowsep="0"><entry>45/49</entry><entry>43/48</entry><entry>12/14</entry><entry>P: 41/41</entry><entry>P:</entry><entry>P:</entry></row><row rowsep="0"><entry>P: 0/0</entry><entry>P: 0/1</entry><entry>P:</entry><entry /><entry>46/48</entry><entry>46/47</entry></row><row><entry /><entry /><entry /><entry>32/35</entry><entry /><entry /><entry /></row><row rowsep="0"><entry morerows="2">T-cell malignancies (n=18)</entry><entry>C: 2/2</entry><entry>C: 0/0</entry><entry>C: 0/0</entry><entry>C: 17/17^c</entry><entry>C:</entry><entry>C: 2/3</entry></row><row rowsep="0"><entry>P:</entry><entry>P:</entry><entry>P:</entry><entry>P: 1/1</entry><entry>15/16^b</entry><entry>P_:</entry></row><row><entry>15/16^e</entry><entry>17/18</entry><entry>17/18</entry><entry /><entry>P: 1/2</entry><entry>14/15^e</entry></row><row rowsep="0"><entry morerows="2" rowsep="1">Reactive samples (n=15)</entry><entry>C: 0/0</entry><entry>C: 0/0</entry><entry>C: 0/0</entry><entry>C: 0/0</entry><entry>C: 0/0</entry><entry>C: 0/0</entry></row><row><entry rowsep="0">P:</entry><entry rowsep="0">P:</entry><entry rowsep="0">P:</entry><entry rowsep="0">P: 14/15</entry><entry rowsep="0">P:</entry><entry rowsep="0">P:</entry></row><row rowsep="0"><entry rowsep="1">15/15</entry><entry rowsep="1">15/15</entry><entry rowsep="1">15/15</entry><entry rowsep="1" /><entry rowsep="1">15/15</entry><entry rowsep="1">15/15</entry></row><row rowsep="0"><entry morerows="1">Miscellaneous (n=8)</entry><entry>C: 3/3</entry><entry>C: 2/2</entry><entry>C: 0/0</entry><entry>C: 3/3</entry><entry>C: 1/1</entry><entry>C: 1/1</entry></row><row><entry>P: 3/5</entry><entry>P: 4/6</entry><entry>P: 6/8</entry><entry>P: 5/5^d,d</entry><entry>P: 6/7</entry><entry>P: 5/7</entry></row><row rowsep="0"><entry morerows="2">All samples (n=90)</entry><entry>C:</entry><entry>C:</entry><entry>C:</entry><entry>C: 25/29</entry><entry>C:</entry><entry>C: 5/6</entry></row><row rowsep="0"><entry>50/54</entry><entry>45/50</entry><entry>12/14</entry><entry>P: 60/61</entry><entry>16/18</entry><entry>P:</entry></row><row rowsep="0"><entry>P:</entry><entry>P:</entry><entry>P:</entry><entry /><entry>P:</entry><entry>80/84</entry></row><row><entry /><entry>33/36</entry><entry>36/40</entry><entry>70/76</entry><entry /><entry>68/72</entry><entry /></row></tbody></tgroup><tgroup cols="7" rowsep="0"><colspec colnum="1" colname="col1" colwidth="26mm" /><colspec colnum="2" colname="col2" colwidth="24mm" /><colspec colnum="3" colname="col3" colwidth="23mm" /><colspec colnum="4" colname="col4" colwidth="22mm" /><colspec colnum="5" colname="col5" colwidth="23mm" /><colspec colnum="6" colname="col6" colwidth="25mm" /><colspec colnum="7" colname="col7" colwidth="25mm" /><tbody><row><entry namest="col1" nameend="col7" align="justify">a. Includes both VH-JH and DH-JH PCR analysis b. C, clonal rearrangements; P, polyclonal rearrangements c. In one sample clonality in GeneScanning only d. In one sample clonality in heteroduplex analysis only e. In one sample polyclonality in GeneScanning only f. In one sample polyclonality in heteroduplex analysis only</entry></row></tbody></tgroup></table></tables><tables id="tabl0012" num="0012"><table frame="all"><title><b>Table 9. Complementarity of different Ig multiplex PCR targets for clonality detection in Southern blot-defined B-cell malignancies</b></title><tgroup cols="5"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="33mm" /><colspec colnum="3" colname="col3" colwidth="32mm" /><colspec colnum="4" colname="col4" colwidth="35mm" /><colspec colnum="5" colname="col5" colwidth="35mm" /><thead><row><entry valign="top">Multiplex PCR tubes</entry><entry namest="col2" nameend="col5" align="center" valign="top">Diagnosis^a</entry></row><row><entry valign="top" /><entry valign="top">Pre-germinal center B (n=8)</entry><entry valign="top">B-CLL (n=16)</entry><entry valign="top">(post-)germinal center B (n=25)</entry><entry valign="top">all B-cell malignancies (n=49)</entry></row></thead><tbody><row><entry><i>IGH</i> VH-JH FR1</entry><entry>8/8^b (100 %)</entry><entry>14/16^c (88 %)</entry><entry>15/25^b (60 %)</entry><entry>37/49 (76 %)</entry></row><row><entry><i>IGH</i> VH-JH FR2</entry><entry>8/8 (100 %)</entry><entry>15/16 (94 %)</entry><entry>14/25^b (56 %)</entry><entry>37/49 (76 %)</entry></row><row><entry><i>IGH</i> VH-JH FR3</entry><entry>8/8 (100 %)</entry><entry>14/16 (88 %)</entry><entry>11/25^c (44 %)</entry><entry>33/49 (67 %)</entry></row><row><entry><i>IGH</i> VH-JH 3FR</entry><entry>8/8 (100 %)</entry><entry>15/16 (94 %)</entry><entry>17/25 (68 %)</entry><entry>40/49 (82 %)</entry></row><row><entry><i>IGH</i> D_H-J_H</entry><entry>0/8 (0 %)</entry><entry>11/16 (69 %)</entry><entry>11/25 (44 %)</entry><entry>22/49 (45 %)</entry></row><row><entry><i>IGH</i> VH-JH + <i>IGH</i> DH-JH</entry><entry>8/8 (100 %)</entry><entry>15/16 (94 %)</entry><entry>22/25 (88 %)</entry><entry>45/49 (92 %)</entry></row><row><entry><i>IGK</i></entry><entry>8/8 (100 %)</entry><entry>16/16 (100 %)</entry><entry>21/25^d (84 %)</entry><entry>45/49 (92 %)</entry></row><row><entry><i>IGL</i></entry><entry>4/8 (50 %)</entry><entry>7/16^e (44 %)</entry><entry>4/25^f (16 %)</entry><entry>15/49 (31 %)</entry></row><row><entry><i>IGH</i> VH-JH + <i>IGK</i></entry><entry>8/8 (100 %)</entry><entry>16/16 (100 %)</entry><entry>21/25 (84 %)</entry><entry>45/49 (92 %)</entry></row><row><entry><i>IGH</i> VH-JH + <i>IGL</i></entry><entry>8/8 (100 %)</entry><entry>15/16 (94 %)</entry><entry>17/25 (68 %)</entry><entry>40/49 (82 %)</entry></row><row><entry><i>IGH</i> VH-JH + <i>IGH</i> DH-JH + <i>IGK</i></entry><entry>8/8 (100 %)</entry><entry>16/16 (100 %)</entry><entry>24/25 (96 %)</entry><entry>48/49 (98 %)</entry></row><row><entry><i>IGH</i> VH-JH + <i>IGH</i> DH-JH + <i>IGK</i> + <i>IGL</i></entry><entry>8/8 (100 %)</entry><entry>16/16 (100 %)</entry><entry>24/25 (96 %)</entry><entry>48/49 (98 %)</entry></row></tbody></tgroup><tgroup cols="5" rowsep="0"><colspec colnum="1" colname="col1" colwidth="32mm" /><colspec colnum="2" colname="col2" colwidth="33mm" /><colspec colnum="3" colname="col3" colwidth="32mm" /><colspec colnum="4" colname="col4" colwidth="35mm" /><colspec colnum="5" colname="col5" colwidth="35mm" /><tbody><row><entry namest="col1" nameend="col5" align="justify">a. All samples have clonal gene rearrangements in at least the <i>IGH</i> locus as determined by Southern blot analysis b. Two cases showed clonal products in GeneScanning, but polyclonal products in heteroduplex analysis c. One case showed clonal products in GeneScanning, but polyclonal products in heteroduplex analysis d. Including case 25-NL-4 with weak clonal <i>IGH</i> but polyclonal <i>IGK</i> gene rearrangements in Southern blot analysis e. Including cases 11-NL-19 and 12-ES-1 with clonal <i>IGH</i> + <i>IGK</i> but polyclonal <i>IGL</i> gene rearrangements in Southern blot analysis</entry></row></tbody></tgroup></table></tables><tables id="tabl0013" num="0013"><table frame="topbot"><title><b>Table 10. Conditions and control samples for multiplex PCR analysis of Ig / TCR gene rearrangements and translocations t(11;14) and t(14;18)</b></title><tgroup cols="7" colsep="0"><colspec colnum="1" colname="col1" colwidth="23mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><colspec colnum="3" colname="col3" colwidth="24mm" /><colspec colnum="4" colname="col4" colwidth="26mm" /><colspec colnum="5" colname="col5" colwidth="24mm" /><colspec colnum="6" colname="col6" colwidth="24mm" /><colspec colnum="7" colname="col7" colwidth="24mm" colsep="1" /><thead><row><entry morerows="1" valign="top">Multiplex PCR</entry><entry morerows="1" valign="top">Tubes</entry><entry namest="col3" nameend="col5" align="center" valign="top">PCR conditions</entry><entry namest="col6" nameend="col7" align="center" valign="top">Positive controls (examples)</entry></row><row><entry valign="top">Buffer</entry><entry valign="top"><i>Taq</i>Gold (U)</entry><entry valign="top">MgCl₂ (mM)</entry><entry valign="top">polyclonal</entry><entry valign="top">monoclonal^a</entry></row></thead><tbody><row rowsep="0"><entry><i>IGH</i> VH-</entry><entry>A / B /</entry><entry>Gold /</entry><entry>1</entry><entry>1.5</entry><entry>tonsil</entry><entry>A: NALM-6;</entry></row><row rowsep="0"><entry>JH</entry><entry>C</entry><entry>II</entry><entry /><entry /><entry /><entry>SU-DHL-5;</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>SU-DHL-6</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>B: NALM-6;</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>SU-DHL-5;</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>SU-DHL-6</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>C: NALM-6;</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>SU-DHL-5;</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>SU-DHL-6</entry></row><row rowsep="0"><entry><i>IGH</i> DH-</entry><entry>D / E</entry><entry>Gold</entry><entry>1</entry><entry>1.5</entry><entry>tonsil</entry><entry>D: KCA; ROS15</entry></row><row rowsep="0"><entry>JH</entry><entry /><entry /><entry /><entry /><entry /><entry>E: HSB-2, HPB-ALL</entry></row><row rowsep="0"><entry><i>IGK</i></entry><entry>A / B</entry><entry>Gold / II</entry><entry>1</entry><entry>1.5</entry><entry>tonsil</entry><entry>A: KCA; ROS15 B: ROS15, 380</entry></row><row rowsep="0"><entry><i>IGL</i></entry><entry>A</entry><entry>Gold / II</entry><entry>1</entry><entry>2.5</entry><entry>tonsil</entry><entry>A: CLL-1; EB-4B; KCA</entry></row><row rowsep="0"><entry><i>TCRB</i></entry><entry>A / B / C</entry><entry>II</entry><entry>2 (A,B)^b 1 (C)</entry><entry>3.0 (A,B) 1.5 (C)</entry><entry>PB-MNC^c</entry><entry>A: RPMI-8402; Jurkat; PEER; DND-41</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>B: PEER; CML-T1, MOLT-3</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>C: Jurkat</entry></row><row rowsep="0"><entry><i>TCRG</i></entry><entry>A / B II</entry><entry /><entry>1</entry><entry>1.5</entry><entry>PB-MNC^c</entry><entry>A: MOLT-3; RPMI-8402; Jurkat; PEER</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>B: Jurkat; PEER</entry></row><row rowsep="0"><entry><i>TCRD</i></entry><entry>A</entry><entry>II</entry><entry>1</entry><entry>2.0</entry><entry>PB-MNC^c</entry><entry>A: PEER, REH</entry></row><row rowsep="0"><entry><i>BCL1-IGH</i></entry><entry>A</entry><entry>II</entry><entry>1</entry><entry>2.0</entry><entry>NA^c</entry><entry>A: JVM 2</entry></row><row rowsep="0"><entry><i>BCL2-IGH</i></entry><entry>A / B / C</entry><entry>II</entry><entry>1</entry><entry>1.5</entry><entry>NA^c</entry><entry>A: DoHH2; SU-DHL-6</entry></row><row rowsep="0"><entry /><entry /><entry /><entry /><entry /><entry /><entry>B: K231^d</entry></row><row><entry /><entry /><entry /><entry /><entry /><entry /><entry>C: OZ; SC1^d; SU-DHL-16</entry></row></tbody></tgroup><tgroup cols="7" rowsep="0"><colspec colnum="1" colname="col1" colwidth="23mm" /><colspec colnum="2" colname="col2" colwidth="23mm" /><colspec colnum="3" colname="col3" colwidth="24mm" /><colspec colnum="4" colname="col4" colwidth="26mm" /><colspec colnum="5" colname="col5" colwidth="24mm" /><colspec colnum="6" colname="col6" colwidth="24mm" /><colspec colnum="7" colname="col7" colwidth="24mm" /><tbody><row><entry namest="col1" nameend="col7" align="justify">a. Most clonal cell line controls can be obtained via the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH; contact person: dr. H.G. Drexler (address: Department of Human and Animal Cell Cultures, Mascheroder Weg 1B, 38124 Braunschweig, Germany). ^192,193 b. In most multiplex tubes only 1 U <i>Taq</i>Gold is needed, but 2 U <i>Taq</i>Gold are needed in <i>TCRB</i> tubes A and B because they contain >15 different primers. c. Abbreviations: PB-MNC, mononuclear cells from peripheral blood; NA, not applicable. d. The t(14;18) positive cell lines K231, OZ, and SC1 were kindly provided by prof. Martin Dyer, University of Leicester, Leicester, GB.</entry></row></tbody></tgroup></table></tables><tables id="tabl0014" num="0014"><table frame="all"><title><b>Table 11. Size ranges, non-specific bands, and detection method in multiplex PCR analysis of Ig/TCR gene rearrangements and chromosome aberrat</b>i<b>ons t(11;14) and t(14;18)</b></title><tgroup cols="6"><colspec colnum="1" colname="col1" colwidth="29mm" /><colspec colnum="2" colname="col2" colwidth="29mm" colsep="0" /><colspec colnum="3" colname="col3" colwidth="27mm" /><colspec colnum="4" colname="col4" colwidth="29mm" /><colspec colnum="5" colname="col5" colwidth="27mm" /><colspec colnum="6" colname="col6" colwidth="28mm" /><thead><row><entry valign="top"><b>Multipl ex PCR</b></entry><entry namest="col2" nameend="col3" align="left" valign="top"><b>Size range (bp)</b></entry><entry valign="top"><b>Nonspecific bands (bp)</b></entry><entry valign="top"><b>Preferred method of analysis</b></entry><entry valign="top"><b>GeneScan running time: gel/capilla ry</b></entry></row></thead><tbody><row rowsep="0"><entry><i>IGH</i></entry><entry><b>Tube A:</b></entry><entry>310-360</entry><entry><b>Tube A:</b> ∼85</entry><entry morerows="2" rowsep="1">GeneScanning and heteroduplex analysis equally suitable</entry><entry>3 - 3.5 h /</entry></row><row rowsep="0"><entry>VH-JH</entry><entry><b>Tube B:</b></entry><entry>250-295</entry><entry><b>Tube B:</b> -</entry><entry>45 min</entry></row><row><entry /><entry><b>Tube C:</b></entry><entry>100-170</entry><entry><b>Tube C:</b> -</entry><entry /></row><row rowsep="0"><entry><i>IGH</i> DH-JH</entry><entry><b>Tube D:</b></entry><entry>110-290 (D_H1/2/4/5/6-J_H)</entry><entry><b>Tube D:</b> 350^a</entry><entry morerows="2" rowsep="1">heteroduplex analysis slightly preferred over GeneScanning (variation of product sizes hampers GeneScanning)</entry><entry>3 - 3.5 h / 45 min</entry></row><row rowsep="0"><entry /><entry /><entry>+390-420 (D_H3-J_H)</entry><entry><b>Tube E:</b> 211^b</entry><entry /></row><row><entry /><entry><b>Tube E:</b></entry><entry>100-130</entry><entry /><entry /></row><row rowsep="0"><entry><i>IGK</i></entry><entry><b>Tube A:</b></entry><entry>120-160 (Vκ1f/6/Vκ7-Jκ) +190-210 (Vκ3f-Jκ) +260-300</entry><entry><b>Tube A:</b> -</entry><entry morerows="2" rowsep="1">heteroduplex analysis slightly preferred over GeneScanning (small junction size + variation of product sizes hampers GeneScanning)</entry><entry>3 - 3.5 h / 45 min</entry></row><row rowsep="0"><entry /><entry /><entry>(Vκ2f/Vκ4/Vκ5-J_κ)</entry><entry><b>Tube B:</b> ∼404</entry><entry /></row><row><entry /><entry><b>Tube B:</b></entry><entry>210-250 Vκlf/6/Vκ7-Kde +270-300 (Vκ3f/intron-Kde) +350-390 (Vκ2f/Vκ4/Vκ5-Kde)</entry><entry /><entry /></row><row><entry><i>IGL</i></entry><entry><b>Tube A:</b></entry><entry>140-165</entry><entry><b>Tube A:</b> -</entry><entry>heteroduplex analysis clearly preferred over GeneScanning (small junction size hampers GeneScanning)</entry><entry>2 h / 45 min</entry></row><row rowsep="0"><entry><i>TCRB</i></entry><entry><b>Tube A:</b></entry><entry>240-285</entry><entry><b>Tube A:</b></entry><entry morerows="4" rowsep="1">heteroduplex analysis slightly preferred over GeneScanning (limited repertoire, particularly in case of ψVγ10 and ψVγ11 usage)</entry><entry>2 h / 45 min</entry></row><row rowsep="0"><entry /><entry><b>Tube B:</b></entry><entry>240-285</entry><entry>(273)^c</entry><entry /></row><row rowsep="0"><entry /><entry><b>Tube C:</b></entry><entry>170-210 (Dβ2)</entry><entry><b>Tube B:</b></entry><entry /></row><row rowsep="0"><entry /><entry /><entry>+ 285-325 (Dβ1)</entry><entry><150, 221^d</entry><entry /></row><row><entry /><entry /><entry /><entry><b>Tube C:</b> 128, 337^d</entry><entry /></row><row rowsep="0"><entry><i>TCRG</i></entry><entry><b>Tube A:</b></entry><entry>145-255</entry><entry><b>Tube A:</b> -</entry><entry morerows="1" rowsep="1">GeneScanning and heteroduplex analysis equally suitable</entry><entry>2 h / 45 min</entry></row><row><entry /><entry><b>Tube B:</b></entry><entry>80-220</entry><entry><b>Tube B:</b> -</entry><entry /></row><row><entry><i>TCRD</i></entry><entry><b>Tube A:</b></entry><entry>120-280</entry><entry><b>Tube A:</b> ∼90</entry><entry>heteroduplex analysis clearly preferred over GeneScanning (low amount of template + variation of product sizes hampers GeneScanning)</entry><entry>2 h / 45 min</entry></row><row><entry><i>BCL1-IGH</i></entry><entry><b>Tube A:</b></entry><entry>150-2000</entry><entry><b>Tube A:</b> ∼550 (weak)</entry><entry>agarose</entry><entry>NA^e</entry></row><row rowsep="0"><entry><i>BCL2-</i></entry><entry><b>Tube A:</b></entry><entry>variable</entry><entry><b>Tube A:</b></entry><entry>agarose</entry><entry>NA^e</entry></row><row rowsep="0"><entry><i>IGH</i></entry><entry><b>Tube B:</b></entry><entry>variable</entry><entry><b>Tube B:</b> -</entry><entry /><entry /></row><row><entry /><entry><b>Tube C:</b></entry><entry>variable</entry><entry><b>Tube C:</b> -</entry><entry /><entry /></row></tbody></tgroup><tgroup cols="6" rowsep="0"><colspec colnum="1" colname="col1" colwidth="29mm" /><colspec colnum="2" colname="col2" colwidth="29mm" /><colspec colnum="3" colname="col3" colwidth="27mm" /><colspec colnum="4" colname="col4" colwidth="29mm" /><colspec colnum="5" colname="col5" colwidth="27mm" /><colspec colnum="6" colname="col6" colwidth="28mm" /><tbody><row><entry namest="col1" nameend="col6" align="justify">a. The nonspecific 350 bp band is the result of cross-annealing of the D_H2 primer to a sequence in the region upstream of J_H4. In GeneScanning this nonspecific band does not comigrate with D-J products (see <figref idref="f0006">Figure 5B</figref>). b. The 211 bp PCR product represents the smallest background band derived from the germline D_H7-J_H1 region. When the PCR amplification is very efficient, also longer PCR products might be obtained because of primer annealing to downstream J_H gene rearrangements; e.g. 419 bp (D_H7-J_H2), 1031 bp (D_H7-J_H3), etc. c.The 273 bp band (mainly visible by GeneScanning) is particularly seen in samples with low numbers of contaminating lymphoid cells. d. Intensity of non-specific band depends on primer quality. e. NA, not applicable</entry></row></tbody></tgroup></table></tables>