Differential roles of Fas ligand in spontaneous and actively induced autoimmune encephalomyelitis

被引:7
|
作者
Liu, TST [1 ]
Hilliard, B
Samoilova, EB
Chen, Y
机构
[1] Univ Penn, Sch Med, Inst Human Gene Therapy, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
关键词
brain; EAE/MS; autoimmunity; Fas (CD95); apoptosis;
D O I
10.1006/clim.2000.4861
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To determine the roles of Fas/Fas ligand (FasL) in autoimmunity, we studied spontaneous and actively induced autoimmune encephalomyelitis in 541 myelin basic protein-specific T cell receptor transgenic mice. We found that spontaneous autoimmune encephalomyelitis, which was initiated by unidentified microbial factors, was dramatically exacerbated in mice carrying Fas or Fast gene mutation. The exacerbation of autoimmune encephalomyelitis was reflected primarily by an increase in disease incidence and a decrease in spontaneous disease recovery. By contrast, actively induced encephalomyelitis, which was initiated by pertussis toxin, was significantly inhibited by Fas or Fast gene mutation. These results suggest that environmental factors that trigger autoimmune disease may determine not only whether disease will occur but also whether an immune molecule such as Fast will promote or inhibit the autoimmune process. (C) 2000 Academic Press.
引用
收藏
页码:203 / 211
页数:9
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