The role of Fas-FasL in CD8+ T-cell-mediated insulin-dependent diabetes mellitus (IDDM)

被引:16
|
作者
Kreuwel, HTC [1 ]
Sherman, LA [1 ]
机构
[1] Scripps Res Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
CD8(+) T cells; autoimmune diabetes; perforin; FasFasL; transgenic mice;
D O I
10.1023/A:1006780629564
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the past few years a number of studies have evaluated the contributions of different cytolytic pathways in the autoimmune destruction of pancreatic beta cells, which results in insulin-dependent (type 1) diabetes mellitus. Conflicting results continue to emerge regarding the role of Fas-mediated apoptosis in beta-cell destruction. This is likely to reflect differences inherent to the model systems under investigation, as well as the pleiotropic nature of the genes that are involved in cytotoxicity. Despite these complications, it may be possible to reconcile some of these apparently conflicting results by considering that T-cell-mediated cytotoxicity can occur simultaneously by several mechanisms and that variables such as the cytokine milieu and the strength of the signal to the T cell received through the T-cell receptor complex may alter the relative contribution of each cytolytic pathway to beta-cell destruction.
引用
收藏
页码:15 / 18
页数:4
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