Haring Jodie S, Pewe Lecia L, Perlman Stanley
Department of Microbiology, University of Iowa, Iowa City, IA 52242, USA.
J Immunol. 2002 Aug 1;169(3):1550-5. doi: 10.4049/jimmunol.169.3.1550.
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.
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。