Follicular regulatory T cells expressing Foxp3 and Bcl-6 suppress germinal center reactions

被引:888
作者
Chung, Yeonseok [1 ,2 ]
Tanaka, Shinya [1 ]
Chu, Fuliang [3 ]
Nurieva, Roza I. [1 ]
Martinez, Gustavo J. [1 ]
Rawal, Seema [3 ]
Wang, Yi-Hong [1 ]
Lim, Hoyong [2 ]
Reynolds, Joseph M. [1 ]
Zhou, Xiao-hui [4 ]
Fan, Hui-min [4 ]
Liu, Zhong-ming [4 ]
Neelapu, Sattva S. [3 ]
Dong, Chen [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Ctr Canc Immunol Res, Houston, TX 77030 USA
[2] Univ Texas Hlth Sci Ctr Houston, Inst Mol Med, Ctr Immunol & Autoimmune Dis, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Ctr Canc Immunol Res, Houston, TX 77030 USA
[4] Shanghai Dong Fang Hosp, Shanghai, Peoples R China
基金
美国国家卫生研究院;
关键词
CXC CHEMOKINE RECEPTOR-5; TRANSCRIPTION FACTOR; HELPER-CELLS; GENERATION; DIFFERENTIATION; INTERLEUKIN-21; FOLLICLES; BLIMP-1; IRF4; ACTS;
D O I
10.1038/nm.2426
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Foxp3(+) regulatory T (T-reg) cells suppress different types of immune responses to help maintain homeostasis in the body. How T-reg cells regulate humoral immunity, including germinal center reactions, is unclear. Here we identify a subset of Treg cells expressing CXCR5 and Bcl-6 that localize to the germinal centers in mice and humans. The expression of CXCR5 on T-reg cells depends on Bcl-6. These CXCR5(+) Bcl-6(+) T-reg cells are absent in the thymus but can be generated de novo from CXCR5-Foxp3(+) natural T-reg precursors. A lack of CXCR5+ T-reg cells leads to greater germinal center reactions including germinal center B cells, affinity maturation of antibodies and the differentiation of plasma cells. These results unveil a Bcl-6-CXCR5 axis in T-reg cells that drives the development of follicular regulatory T (T-FR) cells that function to inhibit the germinal center reactions.
引用
收藏
页码:983 / U102
页数:7
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