A T cell extrinsic mechanism by which IL-2 dampens Th17 differentiation

被引:7
作者
Anderson, Ana C.
Sullivan, Jenna M.
Tan, Dewar J.
Lee, David H.
Kuchroo, Vijay K.
机构
[1] Brigham & Womens Hosp, Evergrande Ctr Immunol Dis, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Ann Romney Ctr Neurol Dis, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
IL-17; T cells; Macrophages; Cytokines; AUTOIMMUNE ENCEPHALOMYELITIS; INTERLEUKIN-27; INFLAMMATION; DISTINCT; LOCUS; MICE; IDD3; NOD; GENERATION; PATHOLOGY;
D O I
10.1016/j.jaut.2015.02.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Genetic variants in il2 and il2ra have been associated with autoimmune disease susceptibility in both genome-wide association studies (GWAS) in humans and in genetic linkage studies in experimental models of autoimmunity. Specifically, genetic variants resulting in a low IL-2 phenotype are susceptibility alleles while variants resulting in a high IL-2 phenotype are resistance alleles. The association of high IL-2 phenotypes with resistance has been attributed primarily to the T cell intrinsic promotion of regulatory T cell development, maintenance, and function; however, IL-2 can also act T cell intrinsically to dampen differentiation of pathogenic IL-17-producing Th17 cells. Here, we have uncovered a novel T cell extrinsic mechanism whereby IL-2 promotes both IFN-gamma and IL-27 production from tissue resident macrophages which in turn dampen the differentiation of pathogenic Th17 cells. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:38 / 42
页数:5
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