IL-27 Is a Key Regulator of IL-10 and IL-17 Production by Human CD4+ T Cells

被引:225
|
作者
Murugaiyan, Gopal [1 ]
Mittal, Akanksha [1 ]
Lopez-Diego, Rocio [1 ]
Maier, Lisa M. [1 ]
Anderson, David E. [1 ]
Weiner, Howard L. [1 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 183卷 / 04期
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR-BETA; CUTTING EDGE; AUTOIMMUNE INFLAMMATION; DENDRITIC CELLS; T-H-17; CELLS; TGF-BETA; DIFFERENTIATION; INDUCTION; INTERLEUKIN-27; CYTOKINE;
D O I
10.4049/jimmunol.0900568
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although the physiologic pathways that control regulatory T cells (Foxp3-expressing regulatory T cells, IL-10-secreting Tr1 cells) and Th17 cells in rodents have been defined, the factors that control these differentiation pathways in humans are not well understood. In this study, we show that IL-27 promotes the differentiation of IL-10-secreting Tr1 cells while inhibiting Th17 generation and molecules associated with Th17 function. Furthermore, IL-27 inhibits IL-17-polarizing cytokines on dendritic cells, which in turn decrease IL-17 secretion from T cells. Our results demonstrate that IL-27 plays a key role in human T cells by promoting IL-10-secreting Tr1 cells and inhibiting Th17 cells and thus provides a dual regulatory mechanism to control auto-immunity and tissue inflammation. The Journal of Immunology, 2009, 183: 2435-2443.
引用
收藏
页码:2435 / 2443
页数:9
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