Suppressive influences of IFN-α on IL-17 expression in human CD4+T cells

被引:11
作者
Hirohata, Shunsei [1 ]
Shibuya, Hideki [2 ]
Tejima, Satoko [1 ]
机构
[1] Kitasato Univ, Sch Med, Dept Rheumatol & Infect Dis, Kanagawa 2288555, Japan
[2] Tokyo Teishin Hosp, Dept Resp Med, Tokyo 1028798, Japan
关键词
Human; Th17; IFN-alpha; IL-17; RCRC; Fox-P3; ROR-GAMMA-T; TGF-BETA; DIFFERENTIATION; CYTOKINES; RESPONSES; TH1;
D O I
10.1016/j.clim.2009.11.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We examined the direct effects of IFN-alpha. on the development of Th17 with a system using immobilized anti-CD3, which permits activation of CD4+ T cells in the complete absence of accessory cells. Highly purified CD4+ T cells obtained from healthy donors were stimulated with immobilized anti-CD3 with or without IFN-a. IFN-a suppressed the production of IL-17 of immobilized anti-CD3-stimulated CD4+ T cells in a dose-response manner. Accordingly, IFN-alpha inhibited IL-17 mRNA expression in immobilized anti-CD3-stimulated CD4+ T celts. IFN-alpha did not affect the production of TGF-beta or IL-6, but inhibited RORC mRNA expression of anti-CD3-stimutated CD4+ T cells. These results indicate that IFN-alpha suppresses IL-17 expression and Th17 differentiation through down-regulation of RORC mRNA expression. It is therefore suggested that these effects might play a rote in the mode of action of IFN-alpha in the treatment of various inflammatory diseases. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:340 / 344
页数:5
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