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Blood · 2011

Is there a role for antigen selection in mantle cell lymphoma? Immunogenetic support from a series of 807 cases.

СтатьяМногоцентровое исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Hadzidimitriou Anastasia, Agathangelidis Andreas, Darzentas Nikos, Murray Fiona, Delfau-Larue Marie-Helene, Pedersen Lone Bredo, Lopez Alba Navarro, Dagklis Antonis, Rombout Paul, Beldjord Kheira, Kolstad Arne, Dreyling Martin H, Anagnostopoulos Achilles, Tsaftaris Athanasios, Mavragani-Tsipidou Penelope, Rosenwald Andreas, Ponzoni Maurilio, Groenen Patricia, Ghia Paolo, Sander Birgitta, Papadaki Theodora, Campo Elias, Geisler Christian, Rosenquist Richard, Davi Frederic, Pott Christiane, Stamatopoulos Kostas

Аннотация

We examined 807 productive IGHV-IGHD-IGHJ gene rearrangements from mantle cell lymphoma (MCL) cases, by far the largest series to date. The IGHV gene repertoire was remarkably biased, with IGHV3-21, IGHV4-34, IGHV1-8, and IGHV3-23 accounting for 46.3% of the cohort. Eighty-four of 807 (10.4%) cases, mainly using the IGHV3-21 and IGHV4-34 genes, were found to bear stereotyped heavy complementarity-determining region 3 (VH CDR3) sequences and were placed in 38 clusters. Notably, the MCL stereotypes were distinct from those reported for chronic lymphocytic leukemia. Based on somatic hypermutation (SHM) status, 238/807 sequences (29.5%) carried IGHV genes with 100% germ line identity; the remainder (569/807; 70.5%) exhibited different SHM impact, ranging from minimal (in most cases) to pronounced. Shared replacement mutations across the IGHV gene were identified for certain subgroups, especially those using IGHV3-21, IGHV1-8, and IGHV3-23. Comparison with other entities, in particular CLL, revealed that several of these mutations were "MCL-biased." In conclusion, MCL is characterized by a highly restricted immunoglobulin gene repertoire with stereotyped VH CDR3s and very precise SHM targeting, strongly implying a role for antigen-driven selection of the clonogenic progenitors. Hence, an antigen-driven origin of MCL could be envisaged, at least for subsets of cases.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты