Cutting Edge: STAT1 Is Required for IL-6-Mediated Bcl6 Induction for Early Follicular Helper Cell Differentiation

被引:242
|
作者
Choi, Youn Soo [1 ]
Eto, Danelle [1 ]
Yang, Jessica A. [1 ]
Lao, Christopher [1 ]
Crotty, Shane [1 ,2 ,3 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Vaccine Discovery, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92037 USA
[3] Ctr HIV AIDS Vaccine Immunol & Immunogen Discover, La Jolla, CA 92037 USA
来源
JOURNAL OF IMMUNOLOGY | 2013年 / 190卷 / 07期
基金
美国国家卫生研究院;
关键词
CHRONIC VIRAL-INFECTION; CD4; T-CELLS; RESPONSES; FH; INTERLEUKIN-21; GENERATION; LINEAGES; VIRUS; MICE;
D O I
10.4049/jimmunol.1203032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bcl6 is required for CD4 T cell differentiation into T follicular helper cells (Tfh). In this study, we examined the role of IL-6 in early processes of in vivo Tfh differentiation, because the timing and mechanism of action of IL-6 in Tfh differentiation have been controversial in vivo. We found that early Bcl6(+) CXCR5(+) Tfh differentiation was severely impaired in the absence of IL-6; however, STAT3 deficiency failed to recapitulate that defect. IL-6R signaling activates the transcription factor STAT1 specifically in CD4 T cells. Strikingly, we found that STAT1 activity was required for Bcl6 induction and early Tfh differentiation in vivo. IL-6 mediated STAT3 activation is important for downregulation of IL-2Ra to limit Th1 cell differentiation in an acute viral infection. Thus, IL-6 signaling is a major early inducer of the Tfh differentiation program unexpectedly mediated by both STAT3 and STAT1 transcription factors. The Journal of Immunology, 2013, 190: 3049-3053.
引用
收藏
页码:3049 / 3053
页数:5
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