Interleukin-17 in pulmonary host defense

被引:62
作者
Aujla, Shean J. [1 ,2 ]
Dubin, Patricia J. [1 ,2 ]
Kolls, Jay K. [1 ,2 ]
机构
[1] Childrens Hosp Pittsburgh, Div Pulm, Dept Pediat, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Pittsburgh, PA 15213 USA
关键词
cytokines; immunity; T-cells;
D O I
10.1080/01902140701756604
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Interleukin (IL)-17A and IL-17F are produced by a novel class of effector alpha beta T cells called Th17 cells as well as gamma delta T cells are alpha beta IL-17-producing T cells are controlled by the tran.scriplio-n factor ROR gamma t and develop independent of GATA-3, T-bet, Stat 4, and Stat 6. Effector molecules produced by these cells include IL-17A, IL-17F, anal IL-22. IL-17A and IL-17F bind to IL-17 receptor (IL-17R) and receptor signaling is critical for host defense against, extracellular bacteria by regulating chemokine gradients for neutrophil emigration into infected tissue sites as well as via regulation of host granulopoiesis. Furthermore, it has recently been shown, that IL-17 and IL-22 regulate the production of antimicrobial proteins in. epithelium. Although Th17 cells are important in nntcosal host defense, in, the setting of retained antigenic stimulation, such as in the setting of asthma or chronic infection, such as in cystic fibrosis, or in the selling of autoimmnnity, these cells cart mediate imrnunopathology.
引用
收藏
页码:507 / 518
页数:12
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