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Translating transitions - How to decipher peripheral human B cell development

Review article
Authors Mats Bemark
Published in Journal of Biomedical Research
Volume 29
Issue 4
Pages 264-284
ISSN 1674-8301
Publication year 2015
Published at Institute of Biomedicine, Department of Microbiology and Immunology
Pages 264-284
Language en
Links dx.doi.org/10.7555/JBR.29.20150035
Keywords B cell, differentiation
Subject categories Immunology, Immunobiology

Abstract

© 2015 by the Journal of Biomedical Research. During the last two decades our understanding of human B cell differentiation has developed considerably. Our understanding of the human B cell compartment has advanced from a point where essentially all assays were based on the presence or not of class-switched antibodies to a level where a substantial diversity is appreciated among the cells involved. Several consecutive transitional stages that newly formed IgM expressing B cells go through after they leave the bone marrow, but before they are fully mature, have been described, and a significant complexity is also acknowledged within the IgM expressing and class-switched memory B cell compartments. It is possible to isolate plasma blasts in blood to follow the formation of plasma cells during immune responses, and the importance and uniqueness of the mucosal IgA system is now much more appreciated. Current data suggest the presence of at least one lineage of human innate-like B cells akin to B1 and/or marginal zone B cells in mice. In addition, regulatory B cells with the ability to produce IL-10 have been identified. Clinically, B cell depletion therapy is used for a broad range of conditions. The ability to define different human B cell subtypes using flow cytometry has therefore started to come into clinical use, but as our understanding of human B cell development further progresses, B cell subtype analysis will be of increasing importance in diagnosis, to measure the effect of immune therapy and to understand the underlying causes for diseases. In this review the diversity of human B cells will be discussed, with special focus on current data regarding their phenotypes and functions.

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Denna text är utskriven från följande webbsida:
http://www.gu.se/english/research/publication/?publicationId=227320
Utskriftsdatum: 2019-09-21