The Coinhibitory Receptor CTLA-4 Controls B Cell Responses by Modulating T Follicular Helper, T Follicular Regulatory, and T Regulatory Cells

被引:328
作者
Sage, Peter T. [1 ,2 ,3 ]
Paterson, Alison M. [1 ,2 ,3 ]
Lovitch, Scott B. [1 ,2 ,3 ,4 ]
Sharpe, Arlene H. [1 ,2 ,3 ,4 ]
机构
[1] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Evergrande Ctr Immunol Dis, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
IN-VIVO; ANTIBODY-RESPONSES; DIFFERENTIATION; GENERATION; INDUCTION; SELECTION; IMMUNITY; INHIBIT; TRANS; ICOS;
D O I
10.1016/j.immuni.2014.12.005
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 receptor CTLA-4 has been implicated in controlling B cell responses, but the mechanisms by which CTLA-4 regulates antibody production are not known. Here we showed deletion of CTLA-4 in adult mice increased Tfh and Tfr cell numbers and augmented B cell responses. In the effector phase, loss of CTLA-4 on Tfh cells resulted in heightened B cell responses, whereas loss of CTLA-4 on Tfr cells resulted in defective suppression of antigen-specific antibody responses. We also found that non-Tfr Treg cells could suppress B cell responses through CTLA-4 and that Treg and/or Tfr cells might downregulate B7-2 on B cells outside germinal centers as a means of suppression. Within the germinal center, however, Tfr cells potently suppress B cells through CTLA-4, but with a mechanism independent of altering B7-1 or B7-2. Thus, we identify multifaceted regulatory roles for CTLA-4 in Tfh, Tfr, and Treg cells, which together control humoral immunity.
引用
收藏
页码:1026 / 1039
页数:14
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