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环孢素诱导的自身免疫中T细胞成熟与克隆清除

T-cell maturation and clonal deletion in cyclosporine-induced autoimmunity.

作者信息

Prud'homme G J, Sanders R, Parfrey N A, Ste-Croix H

机构信息

Department of Pathology, McGill University, Montreal, Canada.

出版信息

J Autoimmun. 1991 Apr;4(2):357-68. doi: 10.1016/0896-8411(91)90030-g.

Abstract

In some circumstances cyclosporine (CyA) induces autoimmune phenomena, and a lethal form of syngeneic graft-vs-host disease (SGVHD) can be induced in rats by the administration of CyA. Although several rat strains develop this disease, in this study, we report that of six mouse strains tested, only the DBA/2 strain developed SGVHD. A comparison of the effect of CyA on thymocytic and peripheral T-cell populations revealed that CyA-induced alterations were similar in the two species, although more marked in rats. Notably, CyA-treated syngeneic bone marrow chimeras (SBMC) had transiently increased numbers of peripheral CD4+ CD8+ T-cells, expressing a marker normally limited to thymocytes. Examination of T-cell receptor (TCR) V beta expression in CyA-treated mice revealed a normal pattern of clonal deletion in all strains (including disease-prone DBA/2 mice), suggesting that CyA may induce autoimmunity without blocking intrathymic clonal deletion.

摘要

在某些情况下,环孢素(CyA)会诱发自身免疫现象,给大鼠施用CyA可诱发一种致死性的同基因移植物抗宿主病(SGVHD)。尽管有几种大鼠品系会患上这种疾病,但在本研究中,我们报告称,在测试的六个小鼠品系中,只有DBA/2品系患上了SGVHD。对CyA对胸腺细胞和外周T细胞群体的影响进行比较后发现,CyA诱导的变化在两个物种中相似,尽管在大鼠中更为明显。值得注意的是,经CyA处理的同基因骨髓嵌合体(SBMC)外周CD4+CD8+T细胞数量短暂增加,这些细胞表达一种通常仅限于胸腺细胞的标志物。对经CyA处理的小鼠的T细胞受体(TCR)Vβ表达进行检测发现,所有品系(包括易患疾病的DBA/2小鼠)的克隆缺失模式均正常,这表明CyA可能在不阻断胸腺内克隆缺失的情况下诱发自身免疫。

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