CD45RB(high) CD4(+) T cells from IFN-gamma knockout mice do not induce wasting disease

被引:57
作者
Ito, H [1 ]
Fathman, CG [1 ]
机构
[1] STANFORD UNIV, SCH MED, DEPT MED, DIV RHEUMATOL & IMMUNOL, STANFORD, CA 94305 USA
关键词
wasting disease; IFN-gamma knockout mice; inflammatory bowel disease; T cell subsets (CD45RB); cytokine function (IFN-gamma);
D O I
10.1016/S0896-8411(97)90152-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transfer of CD45RB(high) CD4(+) T cells from normal mice to congenic SCID mice induces wasting disease, a murine model of inflammatory bowel disease. In this model, colonic inflammation is considered to be caused by a disregulated Th1 response, and Th1 cytokines, especially IFN-gamma, have been suggested to play an important role in the pathogenesis of wasting disease. In order to elucidate the potential role of IFN-gamma in the pathogenesis of wasting disease, we transferred CD45RB(high) CD4(+) T cells from IFN-gamma knockout (GKO) mice to congenic SCID mice. The recipient mice were absolutely free of symptoms and clinical signs of disease and showed body-weight gain similar to that seen in normal mice. These data demonstrate the essential and non-redundant role of IFN-gamma in the pathogenesis of wasting disease. (C) 1997 Academic Press Limited.
引用
收藏
页码:455 / 459
页数:5
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