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恶唑酮结肠炎是一种类似于溃疡性结肠炎的Th2型结肠炎模型,由产生白细胞介素-13的自然杀伤T细胞介导。

Oxazolone colitis, a Th2 colitis model resembling ulcerative colitis, is mediated by IL-13-producing NK-T cells.

作者信息

Heller Frank, Fuss Ivan J, Nieuwenhuis Edward E, Blumberg Richard S, Strober Warren

机构信息

Mucosal Immunity Section, Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Immunity. 2002 Nov;17(5):629-38. doi: 10.1016/s1074-7613(02)00453-3.

Abstract

Oxazolone colitis (OC) is an experimental colitis that has a histologic resemblance to human ulcerative colitis. Here we show that IL-13 production is a significant pathologic factor in OC since its neutralization by IL-13Ralpha2-Fc administration prevents colitis. We further show that OC is mediated by NK-T cells since it can be induced neither in mice depleted of NK-T cells nor in mice that cannot present antigen to NK-T cells and mice lacking an NK-T cell-associated TCR. Finally, we show that NK-T cells are the source of the IL-13, since they produce IL-13 upon stimulation by alpha-galactosylceramide, an NK-T cell-specific antigen. These data thus describe a cellular mechanism underlying an experimental colitis that may explain the pathogenesis of ulcerative colitis.

摘要

恶唑酮结肠炎(OC)是一种实验性结肠炎,其组织学特征与人类溃疡性结肠炎相似。我们在此表明,白细胞介素-13(IL-13)的产生是OC中的一个重要病理因素,因为通过给予IL-13Rα2-Fc中和该细胞因子可预防结肠炎。我们进一步表明,OC由自然杀伤T细胞(NK-T细胞)介导,因为在NK-T细胞耗竭的小鼠中、在无法向NK-T细胞呈递抗原的小鼠中以及缺乏与NK-T细胞相关的T细胞受体的小鼠中均无法诱导出OC。最后,我们表明NK-T细胞是IL-13的来源,因为它们在α-半乳糖神经酰胺(一种NK-T细胞特异性抗原)刺激下会产生IL-13。因此,这些数据描述了一种实验性结肠炎背后的细胞机制,这可能解释溃疡性结肠炎的发病机制。

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