Neutralization of interleukin-17 aggravates dextran sulfate sodium-induced colitis in mice

被引:393
|
作者
Ogawa, A [1 ]
Andoh, A [1 ]
Araki, Y [1 ]
Bamba, T [1 ]
Fujiyama, Y [1 ]
机构
[1] Shiga Univ Med Sci, Dept Internal Med, Otsu, Shiga 5202192, Japan
关键词
cytokine; T cell; monocytes/macrophages;
D O I
10.1016/j.clim.2003.09.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We evaluated the effects of rat anti-mouse IL-17 neutralizing monoclonal antibody (mAb) on the development of dextran sulfate sodium (DSS)-induced colitis. Tissue samples were evaluated by standard immunohistochemical procedure. The mucosal mRNA expression of cytokines was analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR). In the mice treated with the anti-IL-17 mAb, the body weight was significantly lower, and anal prolapse and colon shortening were apparent. A histological analysis indicated that the anti-IL-17 mAb markedly enhanced the severity of colitis. The mucosal infiltration of CD4-positive helper T cells and CD11b-positive granulocytes-monocytes was increased in the anti-IL-17 mAb-treated mice. Treatment with the anti-IL-17 mAb increased the mucosal expression of mRNAs of tumor necrosis factor (TNF)-alpha, interferon (IFN)-gamma, IL-6, RANTES, and IP-10. Blocking of IL-17 activity in vivo using the anti-IL-17 mAb enhanced the development of DSS-colitis in mice. This suggests an inhibitory role for IL-17 in the development of DSS-colitis. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 62
页数:8
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