A dominant function for interleukin 27 in generating interleukin 10-producing anti-inflammatory T cells

被引:653
作者
Awasthi, Amit
Carrier, Yijun
Peron, Jean P. S.
Bettelli, Estelle
Kamanaka, Masahito
Flavell, Richard A.
Kuchroo, Vijay K.
Oukka, Mohamed [1 ]
Weiner, Howard L.
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Neurol Dis, Cambridge, MA 02139 USA
[2] Harvard Univ, Brigham & Womens Hosp, Sch Med, Ctr Neurol Dis, Boston, MA 02115 USA
[3] Univ Sao Paulo, Inst Biomed Sci, Dept Immunol, BR-05508900 Sao Paulo, Brazil
[4] Yale Univ, Sch Med, Immunobiol Sect, New Haven, CT 06520 USA
关键词
D O I
10.1038/ni1541
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (T-reg cells) expressing the transcription factor Foxp3 are key in maintaining the balance of immune homeostasis. However, distinct induced T regulatory type 1 ( Tr1) cells that lack Foxp3 expression also regulate T cell function, mainly by producing the immunosuppressive cytokine interleukin 10 (IL-10). However, the factors required for the induction of IL-10-producing suppressive T cells are not fully understood. Here we demonstrate that dendritic cells modified by Treg cells induced the generation of IL-10-producing Tr1 cells. The differentiation of naive CD4(+) T cells into IL-10-producing cells was mediated by IL-27 produced by the T-reg cell-modified dendritic cells, and transforming growth factor-beta amplified the generation of induced IL-10(+) Tr1 cells by IL-27. Thus, IL-27 and transforming growth factor-beta promote the generation of IL-10-producing Tr1 cells.
引用
收藏
页码:1380 / 1389
页数:10
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