The ageing human B cell repertoire: a failure of selection?
Author(s) -
DunnWalters D. K.
Publication year - 2016
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12700
Subject(s) - breakpoint cluster region , repertoire , biology , b cell receptor , b cell , antibody , immunology , gene , memory b cell , negative selection , selection (genetic algorithm) , antigen , microbiology and biotechnology , genetics , genome , artificial intelligence , computer science , physics , acoustics
Summary B cells undergo a number of different developmental stages, from initial formation of their B cell receptor (BCR) genes to differentiation into antibody‐secreting plasma cells. Because the BCR is vital in these differentiation steps, autoreactive and exogenous antigen binding to the BCR exert critical selection pressures to shape the B cell repertoire. Older people are more prone to infectious disease, less able to respond well to vaccination and more likely to have autoreactive antibodies. Here we review evidence of changes in B cell repertoires in older people, which may be a reflection of age‐related changes in B cell selection processes.
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