Germinal center-dependent and -independent memory B cells produced throughout the immune response

被引:53
作者
Viant, Charlotte [1 ]
Wirthmiller, Tobias [1 ]
ElTanbouly, Mohamed A. [1 ]
Chen, Spencer T. [1 ]
Cipolla, Melissa [1 ]
Ramos, Victor [1 ]
Oliveira, Thiago Y. [1 ]
Stamatatos, Leonidas [2 ,3 ]
Nussenzweig, Michel C. [1 ,4 ]
机构
[1] Rockefeller Univ, Lab Mol Immunol, New York, NY 10065 USA
[2] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1124 Columbia St, Seattle, WA 98104 USA
[3] Univ Washington, Dept Global Hlth, Seattle, WA USA
[4] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
SOMATIC HYPERMUTATION; PLASMA-CELLS; ANTIGEN; SELECTION; DIFFERENTIATION; ANTIBODIES; APOPTOSIS; MOUSE; TAIL;
D O I
10.1084/jem.20202489
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory B cells comprise a heterogenous group of cells that differ in origin and phenotype. During the early phases of the immune response, activated B cells can differentiate into IgM-expressing memory cells, short-lived plasma cells, or seed germinal centers (GCs). The memory compartment is subsequently enriched by B cells that have been through several rounds of division and selection in the GC. Here, we report on the use of an unbiased lineage-tracking approach to explore the origins and properties of memory B cell subsets in mice with an intact immune system. We find that activated B cells continue to differentiate into memory B cells throughout the immune response. When defined on the basis of their origins, the memory B cells originating from activated B cells or GCs differ in isotype and overall gene expression, somatic hypermutation, and their affinity for antigen.
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页数:19
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