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VH gene mutation analysis distinguishes a subgroup of chronic lymphocytic leukemia with low-mutated VH genes and inferior outcome.
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology.
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Article in journal (Refereed) Submitted
URN: urn:nbn:se:uu:diva-91899OAI: oai:DiVA.org:uu-91899DiVA: diva2:164773
Available from: 2004-05-12 Created: 2004-05-12Bibliographically approved
In thesis
1. Immunoglobulin Gene Analysis in Chronic Lymphocytic Leukemia: Characterization of New Prognostic and Biological Subsets
Open this publication in new window or tab >>Immunoglobulin Gene Analysis in Chronic Lymphocytic Leukemia: Characterization of New Prognostic and Biological Subsets
2004 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Recent studies have shown that the somatic mutation status of the immunoglobulin (Ig) VH genes can divide chronic lymphocytic leukemia (CLL) into two prognostic subsets, since cases with mutated VH genes display superior survival compared to unmutated cases. Biased VH gene usage has also been reported in CLL which may reflect antigen selection.

We performed VH gene analysis in 265 CLL cases and confirmed the prognostic impact of the VH mutation status. Preferential VH gene usage was also demonstrated in both the mutated and unmutated subset. Interestingly, CLL cases rearranging one particular VH gene, VH3-21, displayed poor outcome despite that two-thirds showed mutated VH genes. Many of the VH3-21 cases expressed λ light chains, rearranged a Vλ2-14 gene, and had homologous complementarity determining region 3s (CDR3s), implying recognition of a common antigen epitope. We believe that the VH3-21 subset comprises an additional CLL entity.

To further explore the B-cell receptors in CLL, we analyzed the VH gene rearrangements and, specifically, the heavy chain CDR3 sequences in 346 CLL cases. We identified six new subgroups with similar HCDR3 features and restricted VL gene usage as in the VH3-21-using group. Our data indicate a limited number of antigen recognition sites in these subgroups and give further evidence for antigen selection in the development of CLL.

Different cutoffs have been suggested to distinguish mutated CLL in addition to the 2% cutoff. Using three levels of somatic mutations, i.e. <2%, 2-5% and >5%, we divided 323 CLLs into subsets with divergent survival. This division revealed a low-mutated subgroup (2-5%) with inferior outcome that would have been masked using the traditional 2% cutoff.

A 1513A/C polymorphism in the P2X7 receptor gene was reported to be more frequent in CLL, but no difference in genotype frequencies was revealed in our 170 CLL cases and 200 controls. However, CLL cases with the 1513AC genotype showed superior survival than 1513AA cases and this was in particular confined to CLL with mutated VH genes.

In summary, we could define new prognostic subgroups in CLL using Ig gene rearrangement analysis. This also allowed us to gain insights in the biology and potential role of antigen involvement in the pathogenesis of CLL.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2004. 44 p.
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 0282-7476 ; 1360
Genetics, chronic lymphocytic leukemia, immunoglobulin genes, VH3-21, CDR3, P2X7, Genetik
National Category
Medical Genetics
urn:nbn:se:uu:diva-4299 (URN)91-554-5992-7 (ISBN)
Public defence
2004-06-03, Rudbecksalen, Rudbecklaboratoriet, Uppsala, 09:15
Available from: 2004-05-12 Created: 2004-05-12Bibliographically approved

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