CYTOKINES IN INTESTINAL INFLAMMATION - PATHOPHYSIOLOGICAL AND CLINICAL CONSIDERATIONS
CYTOKINES IN INTESTINAL INFLAMMATION - PATHOPHYSIOLOGICAL AND CLINICAL CONSIDERATIONS
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DOI:
10.1016/0016-5085(94)90614-9
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发表时间:
1994-02-01
期刊:
影响因子:
29.4
通讯作者:
SARTOR, RB
中科院分区:
文献类型:
--
作者:
SARTOR, RB
I ntestinal inflammatory states, regardless of specific initiating events, share common immunologically mediated pathways of tissue injury and repair. Activation of immune, mesenchymal, and epithelial cells; recruitment of circulating effector cells; tissue damage; and healing are the consequence of a complex balance of soluble biochemical mediators released by activated intestinal cells. These mediators include cytokines, arachidonic acid metabolites, reactive oxygen intermediates, and growth factors that have important regulatory and effector activities relevant to intestinal inflammation. Cytokines are proteins produced by activated immune cells that influence the activity, differentiation, or proliferation of other cells. These proteins play a key role in the pathogenesis of infammatory bowel disease (IBD), but have not yet been investigated in any detail in other intestinal inflammatory conditions.’However, cytokines almost certainly mediate tissue injury in infectious enterocolitis, celiac disease, microscopicicollagenous colitis, graft vs. host disease, eosinophilic gastroenteritis, and ischemicor radiation-induced enterocolitis. This review will briefly discuss the pathophysiological consequences of cytokines, their measurements in intestinal inflammation, and the clinical relevance of these molecules as markers of disease activity and targets for novel therapeutic intervention.