Resistance to glucocorticoid-induced apoptosis in PLP peptide-specific T cell clones from patients with progressive MS

被引:26
作者
Correale, J
Gilmore, W
Li, S
Walsh, J
Bassani, MM
Lund, B
Arias, M
Weiner, LP
机构
[1] Univ So Calif, Dept Neurol, Sch Med, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Mol Microbiol & Immunol, Sch Med, Los Angeles, CA 90033 USA
[3] Inst Neurol Res Dr Raul Carrea, FLENI, Dept Neurol, RA-1428 Buenos Aires, DF, Argentina
[4] Univ So Calif, Dept Cell & Neurobiol, Sch Med, Los Angeles, CA 90033 USA
基金
美国国家卫生研究院;
关键词
multiple sclerosis; apoptosis; glucocorticoids; T cell clones; autoimmunity;
D O I
10.1016/S0165-5728(00)00326-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glucocorticoids (GC) are commonly used to treat inflammatory disorders such as multiple sclerosis (MS) and may exert their immunosuppressive activity by inducing apoptosis in activated lymphocytes. However, unlike relapsing-remitting MS patients, those with progressive disease respond poorly to GC treatment. The data in this communication indicate that PLP peptide specific T cell clones from progressive, but not relapsing-remitting MS patients are resistant to GC-induced apoptosis in vitro, in a fashion associated with expression of B-7 co-stimulatory molecules. Thus, failure to respond to GC treatment may reflect defect in apoptosis that develop during the progressive stages of chronic inflammatory disease. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:197 / 210
页数:14
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