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Commentary Free access | 10.1172/JCI21412

Ig V region restrictions in human chronic lymphocytic leukemia suggest some cases have a common origin

Grant R. Kolar and J. Donald Capra

Program in Molecular Immunogenetics, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.

Address correspondence to: J. Donald Capra, Program in Molecular Immunogenetics, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, Oklahoma 73104, USA. Phone: (405) 271-7210; Fax: (405) 271-8237; E-mail: donald-capra@omrf.ouhsc.edu.

Find articles by Kolar, G. in: JCI | PubMed | Google Scholar

Program in Molecular Immunogenetics, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA.

Address correspondence to: J. Donald Capra, Program in Molecular Immunogenetics, Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, Oklahoma 73104, USA. Phone: (405) 271-7210; Fax: (405) 271-8237; E-mail: donald-capra@omrf.ouhsc.edu.

Find articles by Capra, J. in: JCI | PubMed | Google Scholar

Published April 1, 2004 - More info

Published in Volume 113, Issue 7 on April 1, 2004
J Clin Invest. 2004;113(7):952–954. https://doi.org/10.1172/JCI21412.
© 2004 The American Society for Clinical Investigation
Published April 1, 2004 - Version history
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Abstract

The factors that contribute to the development of B cell chronic lymphocytic leukemia (B-CLL) are unknown, and the groups of individuals at the greatest risk for developing this common leukemia are not well defined. Molecular features are important for classifying cases of B-CLL, and it is now apparent that similarities among Ig rearrangements between patients may give important clues to the origin of this disease.

B-CLL classification depends on histological and molecular features

B cell chronic lymphocytic leukemia (B-CLL) is the most common form of leukemia in Western countries and most frequently manifests with advancing age. It is characterized by a progressive accumulation of small, long-lived, mature lymphocytes in the blood, bone marrow, and lymphoid tissues as classified by the Revised European/American Lymphoma/WHO (REAL/WHO) classification system (1, 2). B-CLL can be staged according Binet (3) or Rai (4). Most B-CLL cells divide slowly and are distinctive in their CD19+CD5+CD23+ phenotype with low levels of surface membrane immunoglobulin (5). There are no clear genetic predispositions to the development of B-CLL or globally consistent chromosomal abnormalities among patients. Consequently, the etiology of the disease has thus far been elusive.

The Binet and Rai systems can be supplemented by recent findings that further subdivide cases of B-CLL. Cases in which Ig rearrangements are somatically hypermutated result in a milder clinical disease course and better overall survival, while cases in which the Ig sequences remain germline are more severe (6–9). Some cases of B-CLL have even been shown to carry out ongoing somatic hypermutation and class-switch recombination subsequent to activation-induced deaminase (AID) expression much as in germinal center cells (6, 10). An inverse correlation of Zap70 or CD38 expression has also been exploited for use in the clinical setting in order to distinguish B-CLLs of differing severity (11–13). Recent studies of gene expression and surface phenotype of B-CLL cells have revealed that most have a memory B cell phenotype (14, 15) regardless of mutation status. While it is possible that B-CLLs originate from an antigen-exposed memory B cell population, it is also conceivable that memory cell characteristics are acquired following transformation.

Common Ig rearrangements between patients are extremely unusual

While the etiology of B-CLL is yet unknown, an important study in this issue of the JCI by Ghiotto et al. (16), which complements previous reports (17, 18) (reviewed in refs. 19, 20), has yielded valuable insights into factors in the development of B-CLL. Ghiotto et al. report that 20% of a large panel of genetically unrelated IgG class-switched B-CLL cases contained identical Ig VJ and VDJ gene segments. For such a finding to occur by chance is extraordinarily remote. The Ig repertoire has the capacity to produce over 3.4 million functional rearrangements ([44VH × 27DH × 6JH] × [46Vκ × 5Jκ] or [36Vλ × 7Jλ]), yet our laboratory has never found a duplicate rearrangement between patients among a library of 10,000 sequences of normal tonsillar Ig transcripts. This suggests that a process of selection has enforced the use of the gene segment combination described by Ghiotto et al. While it is uncommon to find the particular gene segment combinations in patients with IgM+ B-CLL that the authors observed in patients with IgG+ B-CLL (VH4–39, DH6–13, and JH5), we have found that the VH4–39 gene segment has an increased representation in tonsils of aging adults (Kolar and Capra, unpublished observations). Fais et al. (17) found an increased use of unmutated VH1–69 rearrangements in patients with IgM+ B-CLLs that had a restricted set of DH and JH6 gene segments, but later these segments were not found to be increased in normal blood (21). While still unclear, it is possible that individual or tissue-specific gene segment distributions in aging individuals have a role in particular antigen interactions of B-CLL clones.

Clonotypic Igs are seen in other disease processes

Other immunological diseases that have similar widespread clonotypic Ig manifestations have also been shown to be associated with infection or antigen. One such example is essential mixed cryoglobulinemia (EMC), in which monoclonal IgM antibodies are reactive to polyclonal IgG at temperatures lower than 37°C. Long after EMC was discovered, it was found to be associated with hepatitis C virus (HCV) infection (22, 23) and often makes use of the VH1–69 gene segment, as do responses to HCV (24). B-CLL is not associated with HCV infection (25), but the antigen-induced expansion of clonotypic B cells may be similar. Over twenty-five years ago, our laboratory showed that the similarity among heavy chain complementarity-determining regions (CDRs) 2 and 3 in the mixed cryoglobulin rheumatoid factors Pom and Lay (26, 27) was perhaps an early hint of similar results to those reported by Ghiotto et al. in this issue (16). EMC now is thought to arise from CD5– immunocytomas that are considered marginal zone lymphomas. It is noteworthy that one of the patients described by Ghiotto et al. was identified as an immunocytoma case. Indeed, monoclonal cryoglobulins are often associated with underlying B-CLL or other lymphoproliferative diseases. In the subset of IgG+ B-CLL sequences reported in the study by Ghiotto et al., the CDR3 amino acid sequences are nearly identical, lending the possibility that they arise as a result of similar mechanisms.

Foreign or autoantigens may play a role in B-CLL

It remains to be determined, however, in the case of B-CLL whether a foreign or autoantigen is involved and what role it plays in the progression of the disease (Figure 1). The similarity of Ig clones that have been encountered in the Ghiotto et al. study (16) may provide an important clue to the identification of the antigen. Using Ars as an immunogen, our laboratory showed many years ago that the same Ig rearrangements were used in response to this very small hapten in spite of being isolated from different (albeit genetically identical) mice (28–31). Such findings have been reported in other systems involving immunization with small haptens. In the arsonate system, the amino acid junction sequences of the rearrangements were identical, and an arginine residue at position 99 of the light chain VJ junction of anti-Ars antibodies was shown to be essential for the antibody to recognize this hapten (32). While certain gene segments have been commonly associated with B-CLL (indeed, this led to the discovery of the VH5 gene segment family, ref. 33), the primary structure of the B cell receptor in B-CLL, particularly IgG clones, appears to be more restricted than has previously been thought. There is ample evidence of highly restricted immune responses from the mouse myelomas to carbohydrates (34), raising the possibility that clonal populations in B-CLL patients may be specific for carbohydrate antigens. Marginal zone B cells appear to be important for polysaccharide responses (35–38) and may be involved in the development of B-CLL.

Antigen may play a role in the progression of class-switched B-CLL in a numFigure 1

Antigen may play a role in the progression of class-switched B-CLL in a number of ways: (A) a foreign agent is recognized by an unmutated B cell and aids in the transformation of the cell once it is internalized, or (B) an unmutated IgG memory cell may serve as a starting point prior to transformation. Alternatively (C or D) B-CLL cells with a particular rearrangement may recognize an autoantigen or foreign antigen and in response expand and undergo class-switch recombination. Freq, frequency; Ag, antigen; CSR, class switch recombination.

Ghiotto et al. (16) discuss features of the antigen-binding domain of the B-CLL clones that were visualized by homology modeling. The remarkable similarity among the entire rearrangement and heavy-light chain combinations also resembles those seen in several model systems in responses to small haptens. Of particular interest is a conserved arginine in the base of the binding pocket (which is the result of a recombination) much like that seen in anti-Ars responses in mice. A prominent bulge on the side of three of the five heavy-chain CDR3s was also evident and may provide an unusual surface for an antibody-antigen interaction.

Studies concerning the role and nature of antigens involved in the natural history of B-CLL will clearly have important clinical implications. B-CLLs appear to originate from existing cells, perhaps in the marginal zone, that have special cell phenotypes, producing antibodies against what is likely a very small ligand. Chronic antigenic stimulation of a defined subset of B cells may play an important role in the development of B-CLL pathogenesis. It is possible that individuals have different genetic predispositions, due to polymorphic variations in their immunoglobulin loci, to developing B-CLL clonal expansions in response to certain antigens. Targeted vaccination or methods to maintain tolerance for particular autoantigens may play an important future role in preventative therapies. More practically, the presence of frequent types of rearrangements raises the possibility of developing anti-idiotypic antibodies or even hapten/antigen–binding cytotoxic drugs that could be used for the targeted delivery of therapeutic agents to leukemic cells.

Footnotes

See the related article beginning on page 1008.

Nonstandard abbreviations used: B cell chronic lymphocytic leukemia (B-CLL); complementarity-determining region (CDR); essential mixed cryoglobulinemia (EMC); hepatitis C virus (HCV).

Conflict of interest: The authors have declared that no conflict of interest exists.

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