Transcriptional regulation of follicular T-helper (Tfh) cells

被引：129

作者：

Liu, Xindong ^{[1
,2
,3
]}

Nurieva, Roza I. ^{[1
,2
,3
]}

Dong, Chen ^{[1
,2
,3
]}

机构：

[1] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77054 USA

[2] Univ Texas MD Anderson Canc Ctr, Ctr Inflammat, Houston, TX 77054 USA

[3] Univ Texas MD Anderson Canc Ctr, Ctr Canc, Houston, TX 77054 USA

来源：

IMMUNOLOGICAL REVIEWS | 2013年 / 252卷

关键词：

dendritic cells; T-cell lineages and subsets; Tfh cells; GERMINAL-CENTER FORMATION; CXC CHEMOKINE RECEPTOR-5; FACTOR BATF CONTROLS; CENTER B-CELL; DENDRITIC CELLS; IN-VIVO; IMMUNE-RESPONSES; BCL6; EXPRESSION; TERNARY COMPLEX; PROVIDE HELP;

D O I：

10.1111/imr.12040

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

T-follicular helper (Tfh) cells are a new subset of effector CD4(+) T cells that are specialized in helping B cells in the germinal center reaction. Tfh cells are distinct from other established CD4(+) T-cell lineages, Th1, Th2, Th17, and T-regulatory cells, in their gene expression profiles. Tfh cell differentiation results from a network of transcriptional regulation by a master transcriptional factor Bcl6 as well as IRF4, c-Maf, Batf, and STAT3/5. During Tfh cell ontogeny, increased CXCR5 expression directs activated T-cell migration to the follicles, and their interaction with B cells leads to Bcl6 upregulation, which helps establish effector and memory Tfh cell program. This review summarizes the recent progress in molecular mechanisms underlying Tfh differentiation and discusses the future perspectives for this important area of research.

引用

页码：139 / 145

页数：7

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