The multifaceted functions of follicular regulatory T cells

被引:35
|
作者
Sage, Peter T. [1 ]
Sharpe, Arlene H. [2 ,3 ,4 ,5 ,6 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Transplantat Res Ctr, Div Renal, Boston, MA 02115 USA
[2] Harvard Med Sch, Blavatnik Inst, Dept Immunol, Boston, MA 02115 USA
[3] Harvard Med Sch, Evergrande Ctr Immunol Dis, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[6] Harvard Med Sch, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
GERMINAL CENTER REACTION; HELPER; RESPONSES; INHIBITION; FOXP3; RATIO;
D O I
10.1016/j.coi.2020.10.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immune system is capable of generating robust antibody responses to foreign antigens during infection and vaccination, while simultaneously limiting antibodies to self-antigens. T follicular regulatory (Tfr) cells are a subset of follicular T cell with specialized roles in regulating humoral immunity. Although Tfr cells have been studied for the past 10 years, their roles have remained elusive. In this review we discuss the current understanding of Tfr cell functions in autoimmunity and how Tfr cells simultaneously control foreign and autoantigen specific antibody responses. We highlight new tools that enable in-depth study of Tfr cells in vivo and recent data suggesting an important role for Tfr cells in limiting participation of autoreactive B cells in germinal centers.
引用
收藏
页码:68 / 74
页数:7
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