Memory B Cells in Mouse Models

被引:24
作者
Bergmann, B. [1 ]
Grimsholm, O. [1 ]
Thorarinsdottir, K. [1 ]
Ren, W. [1 ]
Jirholt, P. [1 ]
Gjertsson, I. [1 ]
Martensson, I. -L. [1 ]
机构
[1] Univ Gothenburg, Dept Rheumatol & Inflammat Res, SE-40530 Gothenburg, Sweden
关键词
HELPER T-CELLS; TERTIARY LYMPHOID STRUCTURES; CLASS SWITCH RECOMBINATION; GERMINAL CENTER FORMATION; PRIMARY IMMUNE-RESPONSE; PLASMA-CELLS; SOMATIC HYPERMUTATION; ANTIBODY-RESPONSES; CLONAL SELECTION; AUTOIMMUNE-DISEASE;
D O I
10.1111/sji.12073
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
One of the principles behind vaccination, as shown by Edward Jenner in 1796, and host protection is immunological memory, and one of the cells central to this is the antigen-experienced memory B cell that responds rapidly upon re-exposure to the initiating antigen. Classically, memory B cells have been defined as progenies of germinal centre (GC) B cells expressing isotype-switched and substantially mutated B cell receptors (BCRs), that is, membrane-bound antibodies. However, it has become apparent over the last decade that this is not the only pathway to B cell memory. Here, we will discuss memory B cells in mice, as defined by (1) cell surface markers; (2) multiple layers; (3) formation in a T cell-dependent and either GC-dependent or GC-independent manner; (4) formation in a T cell-independent fashion. Lastly, we will touch upon memory B cells in; (5) mouse models of autoimmune diseases.
引用
收藏
页码:149 / 156
页数:8
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