Germinal center B cells that acquire nuclear proteins are specifically suppressed by follicular regulatory T cells

被引:14
作者
Ke, Fang [1 ]
Benet, Zachary L. [1 ]
Maz, Mitra P. [2 ]
Liu, Jianhua [2 ]
Dent, Alexander L. [3 ]
Kahlenberg, Joanne Michelle [2 ]
Grigorova, Irina L. [1 ]
Kurosaki, Tomohiro
机构
[1] Univ Michigan Ann Arbor, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
[2] Univ Michigan Ann Arbor, Dept Internal Med, Div Rheumatol, Ann Arbor, MI USA
[3] Indiana Univ Sch Med, Dept Microbiol & Immunol, Indianapolis, IN USA
关键词
follicular regulatory T cells; germinal center b cells; immunologic tolerance; nuclear proteins; Human; Mouse; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RESPONSES; BCL6; MODEL;
D O I
10.7554/eLife.83908
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Follicular regulatory T cells (Tfr) restrict development of autoantibodies and autoimmunity while supporting high-affinity foreign antigen-specific humoral response. However, whether Tfr can directly repress germinal center (GC) B cells that acquire autoantigens is unclear. Moreover, TCR specificity of Tfr to self-antigens is not known. Our study suggests that nuclear proteins contain antigens specific to Tfr. Targeting of these proteins to antigen-specific B cells in mice triggers rapid accumulation of Tfr with immunosuppressive characteristics. Tfr then exert negative regulation of GC B cells with predominant inhibition of the nuclear protein-acquiring GC B cells, suggesting an important role of direct cognate Tfr-GC B cells interactions for the control of effector B cell response.
引用
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页数:22
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