Expression and regulation of IL-22 in the IL-17-producing CD4+T lymphocytes

被引:188
作者
Chung, Yeonseok
Yang, Xuexian
Chang, Seon Hee
Ma, Li
Tian, Qiang
Dong, Chen [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[2] Inst Syst Biol, Seattle, WA 98103 USA
关键词
cytokines; helper T cells; T cell activation; gene regulation;
D O I
10.1038/sj.cr.7310106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
IL-22 is a novel cytokine in the IL-10 family that functions to promote innate immunity of tissues against infection. Although CD4+ helper T lymphocytes (TH) were found as a source of IL-22, the regulation of this cytokine has been poorly understood. Here, we show that IL-22 is expressed at both mRNA and protein levels by a novel subset of TH cells that also makes IL-17. IL-22 and IL-17 were found to be coordinately regulated by TGFP and IL-6 during TH differentiation by real-time PCR as well as ELISA analysis. However, IL-22 does not regulate TH differentiation; exogenous IL-22 or an IL-22 antagonist had no effect on TH differentiation. These data demonstrate a novel cytokine expressed by IL-17-producing T cells, and suggest interaction and synergy of IL-22 and IL-17 signaling pathways in tissue inflammation and autoimmune diseases.
引用
收藏
页码:902 / 907
页数:6
相关论文
共 12 条
[1]   Opinion - Diversification of T-helper-cell lineages: finding the family root of IL-17-producing cells [J].
Dong, C .
NATURE REVIEWS IMMUNOLOGY, 2006, 6 (04) :329-333
[2]   Cell fate decision: T-helper 1 and 2 subsets in immune responses [J].
Dong, C ;
Flavell, RA .
ARTHRITIS RESEARCH, 2000, 2 (03) :179-188
[3]   Regulation of immune and autoimmune responses by ICOS [J].
Dong, C ;
Nurieva, RI .
JOURNAL OF AUTOIMMUNITY, 2003, 21 (03) :255-260
[4]  
Glimcher LH, 2000, GENE DEV, V14, P1693
[5]   Innate immunity gone awry: Linking microbial infections to chronic inflammation and cancer [J].
Karin, M ;
Lawrence, T ;
Nizet, V .
CELL, 2006, 124 (04) :823-835
[6]   IL-23 drives a pathogenic T cell population that induces autoimmune inflammation [J].
Langrish, CL ;
Chen, Y ;
Blumenschein, WM ;
Mattson, J ;
Basham, B ;
Sedgwick, JD ;
McClanahan, T ;
Kastelein, RA ;
Cua, DJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (02) :233-240
[7]   A distinct lineage of CD4 T cells regulates tissue inflammation by producing interleukin 17 [J].
Park, H ;
Li, ZX ;
Yang, XO ;
Chang, SH ;
Nurieva, R ;
Wang, YH ;
Wang, Y ;
Hood, L ;
Zhu, Z ;
Tian, Q ;
Dong, C .
NATURE IMMUNOLOGY, 2005, 6 (11) :1133-1141
[8]   Interleukin-10 and related cytokines and receptors [J].
Pestka, S ;
Krause, CD ;
Sarkar, D ;
Walter, MR ;
Shi, YF ;
Fisher, PB .
ANNUAL REVIEW OF IMMUNOLOGY, 2004, 22 :929-979
[9]   Th17: An effector CD4 T cell lineage with regulatory T cell ties [J].
Weaver, Casey T. ;
Harrington, Laurie E. ;
Mangan, Paul R. ;
Gavrieli, Maya ;
Murphy, Kenneth M. .
IMMUNITY, 2006, 24 (06) :677-688
[10]   IL-22 increases the innate immunity of tissues [J].
Wolk, K ;
Kunz, S ;
Witte, E ;
Friedrich, M ;
Asadullah, K ;
Sabat, R .
IMMUNITY, 2004, 21 (02) :241-254