IL-17 inhibits human Th1 differentiation through IL-12Rβ2 downregulation

被引:40
作者
Toh, Myew-Ling
Kawashima, Masanori
Zrioual, Saloua
Hot, Arnaud
Miossec, Philippe
Miossec, Pierre
机构
[1] Univ Lyon, Edouard Herriot Hosp, Dept Immunol, Immunogen & Inflammat Res Unit EA 4130, Lyon, France
[2] Univ Lyon, Edouard Herriot Hosp, Dept Rheumatol, Immunogen & Inflammat Res Unit EA 4130, Lyon, France
关键词
IL-17; Th17; IL-12R beta 2; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; IL-17-PRODUCING T-CELLS; NF-KAPPA-B; PERIPHERAL-BLOOD; RHEUMATOID-ARTHRITIS; HELPER-CELLS; IN-VIVO; RECEPTOR; EXPRESSION; INFLAMMATION;
D O I
10.1016/j.cyto.2009.07.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Th17 cells are critical in adaptive immunity and autoimmune disease. The polarized development of Th17, Th1 and Th2 cells is dependent on counterregulatory effects on each other. Whereas IFN-gamma inhibits Th17 development, the effect of IL-17 in human Th1 development is not known. We report a novel negative regulatory role of IL-17 on IL-12R beta 2 expression associated with reduced IL-12 responsiveness. IL-17 decreased IL-12-induced IFN-gamma expression in PBMC and developing Th1 cells, associated with a selective reduction in IL-12R beta 2, and not IL-23R, IL-12R beta 1 or T-bet. Counterregulatory effects of human Th17 on Th1 lineage cytokines may contribute to lineage divergence. In autoimmune disease, IL-17 may reinforce its own developmental programme by reducing IL-12 responsiveness, thus limiting inhibitory effects of IFN-gamma on Th17 development. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:226 / 230
页数:5
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