InterIeukin-23/Th17 Pathways and Inflammatory Bowel Disease

被引:234
作者
Abraham, Clara [1 ]
Cho, Judy [1 ]
机构
[1] Yale Univ, Dept Med, New Haven, CT 06520 USA
关键词
inflammatory bowel disease; inflammation; autoimmunity; IL-23; Th17; cells; GENOME-WIDE ASSOCIATION; IL-17-PRODUCING T-CELLS; GROWTH-FACTOR-BETA; ROR-GAMMA-T; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; COLONIC SUBEPITHELIAL MYOFIBROBLASTS; PEDIATRIC CROHNS-DISEASE; CHEMOKINE RECEPTOR CCR6; PROPRIA DENDRITIC CELLS; ULCERATIVE-COLITIS;
D O I
10.1002/ibd.20894
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The IL-23/Th17pathway has recently been identified to play a critical role in a number of chronic inflammatory diseases including inflammatory bowel disease (IBD). The identification in IBD patients of associations in IL23R and regions that include other genes in the IL-23/Th17pathway has highlighted the importance of proper IL-23/Th17pathway regulation in intestinal immune homeostasis. IL-23 plays a role in CD4+ Th17 lineage cells, characterized by IL-17 secretion and the expression of the transcription factor retinoic acid-related orphan receptor (ROR)gamma tau, and in other immune and nonimmune cells. The balance between effector T cell Subsets, Such as Th17cells, and CD4+ T regulatory subsets is finely regulated: dysregulation of this balance can lead to inflammation and autoimmunity. As such, the IL-23/Th17pathway contributes to immune responses that play a role in defenses to microbial infection, as well as in the intestinal inflammation observed in both animal models of colitis and human IBD. (Inflamm Bowel Dis 2009:15:1090-1100)
引用
收藏
页码:1090 / 1100
页数:11
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