Autocrine Transforming Growth Factor-β1 Promotes In Vivo Th17 Cell Differentiation

被引:258
作者
Gutcher, Ilona [1 ]
Donkor, Moses K. [1 ]
Ma, Qian [1 ]
Rudensky, Alexander Y. [1 ,3 ]
Flavell, Richard A. [2 ,3 ]
Li, Ming O. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Program Immunol, New York, NY 10065 USA
[2] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
GROWTH-FACTOR-BETA; REGULATORY T-CELLS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; TGF-BETA; MULTIPLE-SCLEROSIS; INFLAMMATION; LINEAGE; MICE; EXPRESSION; DISEASE;
D O I
10.1016/j.immuni.2011.03.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
TGF-beta 1 is a regulatory cytokine that has an important role in controlling T cell differentiation. T cell-produced TGF-beta 1 acts on T cells to promote Th17 cell differentiation and the development of experimental autoimmune encephalomyelitis (EAE). However, the exact TGF-beta 1-producing T cell subset required for Th17 cell generation and its cellular mechanism of action remain unknown. Here we showed that deletion of the Tgfb1 gene from activated T cells and Treg cells, but not Treg cells alone, abrogated Th17 cell differentiation, resulting in almost complete protection from EAE. Furthermore, differentiation of T cells both in vitro and in vivo demonstrated that TGF-beta 1 was highly expressed by Th17 cells and acted in a predominantly autocrine manner to maintain Th17 cells in vivo. These findings reveal an essential role for activated T cell-produced TGF-beta 1 in promoting the differentiation of Th17 cells and controlling inflammatory diseases.
引用
收藏
页码:396 / 408
页数:13
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