IL-21 regulates Th17 cells in rheumatoid arthritis

被引:120
作者
Niu, Xiaoyin [1 ]
He, Dongyi [2 ]
Zhang, Xin [3 ]
Yue, Tao [2 ]
Li, Ningli [1 ]
Zhang, Jingwu Z. [1 ,3 ]
Dong, Chen [4 ,5 ]
Chen, Guangjie [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Immunol, Inst Med Sci, Shanghai Inst Immunol,Sch Med, Shanghai 200030, Peoples R China
[2] GuangHua Rheumatol Hosp, Dept Rheumatol, Shanghai, Peoples R China
[3] Chinese Acad Sci, Dept Immunol, Inst Hlth Sci, Inst Biol Sci, Shanghai, Peoples R China
[4] MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[5] Tongji Univ, Ctr Immunol & Inflammat, Shanghai, Peoples R China
关键词
Autoimmune disease; Th17; cells; IL-21; Rheumatoid arthritis; INFLAMMATORY-BOWEL-DISEASE; CHEMOKINE RECEPTOR CCR6; COMMON GAMMA-CHAIN; HUMAN T-CELLS; IN-VITRO; AUTOIMMUNE INFLAMMATION; ADAPTIVE IMMUNITY; NK CELLS; ACTIVATION; DIFFERENTIATION;
D O I
10.1016/j.humimm.2010.01.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-21 is a type 1 cytokine that like IL-2, IL-4, IL-7, IL-9, and IL-15 uses the common gamma chain of cytokine receptor. IL-21 has been shown to regulate the function of T cells, B cells, natural killer cells, and dendritic cells in immune responses. Although activated CD4(+) T cells produce IL-21, recent data suggest that novel subsets of effector T cells are the major producers in immune responses. In this study, we show that IL-21 expression correlates with the presence of Th17 cells in synovial fluid (SF) and peripheral blood in rheumatoid arthritis patients. Human CCR6+ CD4(+) T cells produce high levels of both IL-21 and IL-17. Similar to mouse T cells, IL-21 auto-regulates its own production in human CD4(+) T cells. IL-21 potently enhances Th17 proliferation and suppresses Foxp3 expression, leading to the expression of RORC. IL-21 is therefore an autocrine cytokine that regulates human Th17 cells in rheumatoid arthritis, and serves as a good target for treating this autoimmune disease. (C) 2010 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:334 / 341
页数:8
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