Plasma cells negatively regulate the follicular helper T cell program

被引:111
作者
Pelletier, Nadege [1 ]
McHeyzer-Williams, Louise J. [1 ]
Wong, Kurt A. [1 ]
Urich, Eduard [1 ]
Fazilleau, Nicolas [1 ]
McHeyzer-Williams, Michael G. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
MEMORY B-CELLS; GERMINAL-CENTERS; IN-VIVO; DENDRITIC CELLS; BONE-MARROW; LYMPH-NODE; BLIMP-1; DIFFERENTIATION; EXPRESSION; ANTIBODY;
D O I
10.1038/ni.1954
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B lymphocytes differentiate into antibody-secreting cells under the antigen-specific control of follicular helper T cells (T-FH cells). Here we demonstrate that isotype-switched plasma cells expressed major histocompatibility complex (MHC) class II, the costimulatory molecules CD80 and CD86, and the intracellular machinery required for antigen presentation. Antigen-specific plasma cells accessed, processed and presented sufficient antigen in vivo to induce multiple helper T cell functions. Notably, antigen-primed plasma cells failed to induce interleukin 21 (IL-21) or the transcriptional repressor Bcl-6 in naive helper T cells and actively decreased these key molecules in antigen-activated T-FH cells. Mice lacking plasma cells showed altered T-FH cell activity, which provided evidence of this negative feedback loop. Hence, antigen presentation by plasma cells defines a previously unknown layer of cognate regulation that limits the antigen-specific T-FH cell program that controls ongoing B cell immunity.
引用
收藏
页码:1110 / U132
页数:10
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