The cytokine milieu in the interplay of pathogenic Th1/Th17 cells and regulatory T cells in autoimmune disease

被引:183
|
作者
Leung, Stewart [1 ]
Liu, Xuebin [1 ]
Fang, Lei [1 ]
Chen, Xi [1 ]
Guo, Taylor [1 ]
Zhang, Jingwu [1 ]
机构
[1] GlaxoSmithKline Res & Dev Ctr, Dept Neuroimmunol, Shanghai 201203, Peoples R China
关键词
Autoimmune disease; Cytokine; Regulatory T cell; T helper 17 cell; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; IMMUNOLOGICAL SELF-TOLERANCE; MYELIN BASIC-PROTEIN; TRANSCRIPTION FACTOR; RHEUMATOID-ARTHRITIS; TGF-BETA; INTERLEUKIN-7; RECEPTOR; POTENTIAL TREATMENT; TH17; CELLS; IN-VITRO;
D O I
10.1038/cmi.2010.22
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The propagation and regulation of an immune response is driven by a network of effector and regulatory T (Treg) cells. The interplay of effector T and Treg cells determines the direction of the immune response towards inflammation or its resolution in an autoimmune disease setting. In autoimmune diseases, this interplay shifts the balance in favor of the development of autoreactive effector T cells, resulting in inflammatory pathology. The objective of an effective therapeutic approach for autoimmune disease is to restore this balance. In this review, we describe the characteristics and development of pathogenic T helper 1 (Th1) and Th17 cells and the beneficial Treg cells in autoimmune diseases and the crucial roles of the cytokine milieu in influencing the balance of these T-cell subsets. Given the importance of cytokines, we discuss current immunotherapeutic strategies using cytokine or cytokine receptor antibodies for the treatment of autoimmune diseases. Cellular & Molecular Immunology (2010) 7, 182-189; doi:10.1038/cmi.2010.22; published online 12 April 2010
引用
收藏
页码:182 / 189
页数:8
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