The IL-17 pathway as a major therapeutic target in autoimmune diseases

被引:102
作者
Hu, Yan [2 ]
Shen, Fang [1 ]
Crellin, Natasha K. [1 ]
Ouyang, Wenjun [1 ]
机构
[1] Genentech Inc, Dept Immunol, San Francisco, CA 94080 USA
[2] C2N Diagnost, St Louis, MO USA
来源
YEAR IN IMMUNOLOGY | 2011年 / 1217卷
关键词
IL-17; receptors; Th17; host defense; autoimmunity; COLLAGEN-INDUCED ARTHRITIS; TUMOR-NECROSIS-FACTOR; GROWTH-FACTOR-BETA; NF-KAPPA-B; INFLAMMATORY-BOWEL-DISEASE; ACTIVATED PROTEIN-KINASE; CENTRAL-NERVOUS-SYSTEM; T-HELPER-CELLS; HUMAN OSTEOARTHRITIC CHONDROCYTES; COLONY-STIMULATING FACTOR;
D O I
10.1111/j.1749-6632.2010.05825.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Th17 cells are a subset of T helper cells that have been recently found to play important functions in host defense and the pathogenesis of various human autoimmune and inflammatory diseases. Th17 cells produce IL-17A, IL-17F, IL-22, and IL-21, of which IL-17A and IL-17F mediate many of the downstream pathologic functions of these cells. IL-17A and IL-17F signal through IL-17RA and IL-17RC heterodimeric receptors that are mainly expressed on tissue epithelial cells and fibroblasts. While IL-17A and IL-17F are important for host defense against many extracellular pathogens, they can also cause excessive tissue damage and exacerbate proinflammatory responses during autoimmunity. The IL-17 pathway, therefore, is a primary therapeutic target downstream of Th17 cells.
引用
收藏
页码:60 / 76
页数:17
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