Distinct roles of IL-22 in human psoriasis and inflammatory bowel disease

被引:111
作者
Ouyang, Wenjun [1 ]
机构
[1] Genentech Inc, Dept Immunol, San Francisco, CA 94080 USA
关键词
IL-22; IBD; Psoriasis; Th17; GENOME-WIDE ASSOCIATION; NATURAL-KILLER-CELLS; PROINFLAMMATORY GENE-EXPRESSION; ACTIVE CROHNS-DISEASE; II CYTOKINE RECEPTOR; INDUCER-LIKE CELLS; TH17; T-CELLS; ROR-GAMMA-T; SKIN INFLAMMATION; INTESTINAL INFLAMMATION;
D O I
10.1016/j.cytogfr.2010.10.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IL-22, an IL-10 family cytokine, is produced by different leukocyte subsets, including T cells, NK cells and lymphoid tissue inducer (LTi) cells. IL-22 mediates the crosstalk between leukocytes and tissue epithelia because its receptor is preferentially expressed on various tissue epithelial cells. IL-22 is essential for host defense against infections of extracellular pathogens, such as bacteria and yeasts, by eliciting various innate defensive mechanisms from tissue epithelial cells and promoting wound-healing responses. In autoimmune diseases, however, diverse tissue microenvironments and underlying pathogenic mechanisms may result in opposing contributions of IL-22 in disease progression. For example, in psoriasis, IL-22 can synergize with other proinflammatory cytokines to induce many of the pathogenic phenotypes from keratinocytes and exacerbate disease progression. In contrast, IL-22 plays a beneficial role in IBD by enhancing barrier integrity and epithelial innate immunity of intestinal tract. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:435 / 441
页数:7
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