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Interleukin-6 trans-signaling in inflammatory bowel disease

Journal

CYTOKINE & GROWTH FACTOR REVIEWS
Volume 17, Issue 6, Pages 451-461

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cytogfr.2006.09.003

Keywords

interleukin-6; gp130; soluble receptor; sgp130Fc; STAT3; Crohn's disease; ulcerative colitis

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The pathogenesis of inflammatory bowel disease (IBD) is complex, involving a wide range of molecules including cytokines. Recent investigations support the important role of an interleukin-6 (IL-6) signaling pathway in the development of IBD. However, the molecular mechanisms of this pathway in the intestine remain incompletely understood. The circulating and intestinal levels of IL-6 as well as soluble IL-6 receptor (sIL-6R) are increased in patients with IBD. It is remarkable that the mucosal T cells of IBD patients are extremely resistant to apoptosis and that a large fraction of these cells express membrane-bound gp130 but not IL-6R. The accumulated evidence strongly supports the hypothesis that the development and perpetuation of IBD relies on the increased formation of IL-6/sIL-6R complexes interacting with membrane-bound gp130 on T cells via trans-signaling. These studies suggest that IL-6 trans-signaling may play a role in the development of IBD; they therefore imply the possibility of a selective therapeutic strategy to target this signaling. (c) 2006 Elsevier Ltd. All rights reserved.

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