The presence of CLL-associated stereotypic B cell receptors in the normal BCR repertoire from healthy individuals increases with age
Autor: | Rudi W. Hendriks, Elisabeth Brouwer, Annemieke M. H. Boots, Jan A N Verhaar, Wayel H. Abdulahad, Ingrid L. M. Wolvers-Tettero, Nikos Darzentas, Jacques J. M. van Dongen, Anton W. Langerak, Alice F. Muggen, Mirjam van der Burg, Cristina Teodosio, Hanna IJspeert, Wilfred F. J. van IJcken, Madelon de Jong, Ralph Stadhouders, Martine J. Kallemeijn |
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Přispěvatelé: | Translational Immunology Groningen (TRIGR), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Microbes in Health and Disease (MHD), Immunology, Pulmonary Medicine, Cell biology, Clinical Genetics, Orthopedics and Sports Medicine |
Rok vydání: | 2019 |
Předmět: |
lcsh:Immunologic diseases. Allergy
EXPRESSION 0301 basic medicine Aging Chronic lymphocytic leukemia Immunology B-cell receptor DIVERSITY lcsh:Geriatrics B-lymphocyte 03 medical and health sciences 0302 clinical medicine hemic and lymphatic diseases medicine SUBPOPULATIONS B cell biology CHRONIC LYMPHOCYTIC-LEUKEMIA Research breakpoint cluster region HUMANS Immunosenescence Acquired immune system medicine.disease GALAXY lcsh:RC952-954.6 030104 developmental biology medicine.anatomical_structure IMMUNOGLOBULIN biology.protein Stereotypic BCR BCR repertoire Antibody lcsh:RC581-607 IGHV@ CLL 030215 immunology |
Zdroj: | Immunity & Ageing : I & A Immunity & ageing : I & A, 16(1):22. BMC Immunity and Ageing, 16(1):22. BioMed Central Ltd. Immunity and Ageing, 16(1) Immunity & Ageing, Vol 16, Iss 1, Pp 1-12 (2019) |
ISSN: | 1742-4933 |
Popis: | Background Aging is known to induce immunosenescence, resulting in alterations in both the innate and adaptive immune system. Here we evaluated the effects of aging on B cell subsets in peripheral blood of 155 immunologically healthy individuals in four age categories (range 20-95y) via multi-parameter flow cytometry. Furthermore, we studied the naive and antigen-experienced B cell receptor (BCR) repertoire of different age groups and compared it to the clonal BCR repertoire of chronic lymphocytic leukemia (CLL), a disease typically presenting in elderly individuals. Results Total numbers and relative frequencies of B cells were found to decline upon aging, with reductions in transitional B cells, memory cell types, and plasma blasts in the 70 + y group. The BCR repertoire of naive mature B cells and antigen-experienced B cells did not clearly alter until age 70y. Clear changes in IGHV gene usage were observed in naive mature B cells of 70 + y individuals, with a transitional pattern in the 50-70y group. IGHV gene usage of naive mature B cells of the 50-70y, but not the 70 + y, age group resembled that of both younger (50-70y) and older (70 + y) CLL patients. Additionally, CLL-associated stereotypic BCR were found as part of the healthy control BCR repertoire, with an age-associated increase in frequency of several stereotypic BCR (particularly subsets #2 and #5). Conclusion Composition of the peripheral B cell compartment changes with ageing, with clear reductions in non-switched and CD27 + IgG+ switched memory B cells and plasma blasts in especially the 70 + y group. The BCR repertoire is relatively stable until 70y, whereafter differences in IGHV gene usage are seen. Upon ageing, an increasing trend in the occurrence of particular CLL-associated stereotypic BCR is observed. Electronic supplementary material The online version of this article (10.1186/s12979-019-0163-x) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
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