Human mucosal-associated invariant T (MAIT) cells possess capacity for B cell help

被引:66
|
作者
Bennett, Michael S. [1 ,3 ]
Trivedi, Shubhanshi [1 ]
Iyer, Anita S. [1 ]
Hale, J. Scott [2 ]
Leung, Daniel T. [1 ,2 ]
机构
[1] Univ Utah, Sch Med, Div Infect Dis, Dept Internal Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Sch Med, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT 84132 USA
[3] ARUP Labs, ARUP Inst Clin & Expt Pathol, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
plasmablast; B cell help; MR-1; antibody; RECEPTOR HETEROGENEITY; IMMUNE-RESPONSES; ACTIVATION; MR1; PROLIFERATION; MECHANISM; ANTIGENS; INNATE; GAMMA;
D O I
10.1189/jlb.4A0317-116R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human MAIT cells have the capacity to provide help to B cells through induction of plasmablast differentiation and antibody production. Mucosal-associated invariant T (MAIT) cells are an innate-like T cell subset, restricted by the nonclassic MHC class I-related protein MR1 and enriched at mucosal sites. Human studies have shown an association between MAIT cells and pathogen-specific antibody responses. In this study, we investigate the effect of human MAIT cells on B cells ex vivo. We found that supernatants from microbe- or cytokine-stimulated MAIT cells, when added to purified autologous B cells, increase frequencies of plasmablasts and promote IgA, IgG, and IgM production. We found effects to be mostly MR1-dependent and that the increases in plasmablasts are likely a result of increased differentiation from memory B cells. Furthermore, microbe-activated MAIT cell supernatant contains multiple cytokines known to stimulate B cells, including IL-6, -10, and -21. This study thus provides the first direct evidence of a newly identified role of MAIT cells in providing help to B cells.
引用
收藏
页码:1261 / 1269
页数:9
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