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中枢神经系统病毒感染后旁观者CD8 T细胞介导的脱髓鞘作用。

Bystander CD8 T cell-mediated demyelination after viral infection of the central nervous system.

作者信息

Haring Jodie S, Pewe Lecia L, Perlman Stanley

机构信息

Department of Microbiology, University of Iowa, Iowa City, IA 52242, USA.

出版信息

J Immunol. 2002 Aug 1;169(3):1550-5. doi: 10.4049/jimmunol.169.3.1550.

Abstract

Multiple sclerosis, a chronic inflammatory disease of the CNS, is characterized by immune-mediated demyelination. Many patients have a remitting-relapsing course of disease with exacerbations often following unrelated microbial illnesses. The relationship between the two events remains obscure. One possibility is that T cells specific for the inciting microbial pathogen are able to effect demyelination at a site of ongoing inflammation within the CNS. This possibility was examined in mice infected with mouse hepatitis virus, a well-described model of virus-induced demyelination. Using transgenic TCR/recombination activation gene 2(-/-) mice with only non-mouse hepatitis virus-specific T cells, we show that CD8 T cells are able to cause demyelination in the absence of cognate Ag in the CNS, but only if specifically activated. These findings demonstrate a novel mechanism for immune-mediated neuropathology and show that activated CD8 T cells may serve as important mediators of bystander demyelination during times of infection, including in patients with multiple sclerosis.

摘要

多发性硬化症是一种中枢神经系统的慢性炎症性疾病,其特征为免疫介导的脱髓鞘。许多患者的病程呈复发-缓解型,病情加重常发生在无关的微生物感染之后。这两种事件之间的关系仍不清楚。一种可能性是,针对引发感染的微生物病原体的特异性T细胞能够在中枢神经系统内正在发生炎症的部位导致脱髓鞘。在感染小鼠肝炎病毒的小鼠中对这种可能性进行了研究,小鼠肝炎病毒是一种广为人知的病毒诱导脱髓鞘模型。使用仅具有非小鼠肝炎病毒特异性T细胞的转基因T细胞受体/重组激活基因2(-/-)小鼠,我们发现CD8 T细胞能够在中枢神经系统中不存在同源抗原的情况下导致脱髓鞘,但前提是经过特异性激活。这些发现证明了免疫介导的神经病理学的一种新机制,并表明活化的CD8 T细胞可能是感染期间旁观者脱髓鞘的重要介质,包括在多发性硬化症患者中。

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