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病毒扩增的调节性 T 细胞控制多发性硬化症 Theiler 病毒小鼠模型的疾病严重程度。

Virus expanded regulatory T cells control disease severity in the Theiler's virus mouse model of MS.

机构信息

Department of Microbiology-immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

J Autoimmun. 2011 Mar;36(2):142-54. doi: 10.1016/j.jaut.2010.12.005. Epub 2011 Jan 26.

Abstract

Theiler's murine encephalomyelitis virus (TMEV)-induced demyelinating disease (TMEV-IDD) serves as virus-induced model of chronic progressive multiple sclerosis. Infection of susceptible SJL/J mice leads to life-long CNS virus persistence and a progressive autoimmune demyelinating disease mediated by myelin-specific T cells activated via epitope spreading. In contrast, virus is rapidly cleared by a robust CTL response in TMEV-IDD-resistant C57BL/6 mice. We investigated whether differential induction of regulatory T cells (Tregs) controls susceptibility to TMEV-IDD. Infection of disease-susceptible SJL/J, but not B6 mice, leads to rapid activation and expansion of Tregs resulting in an unfavorable CNS ratio of Treg:Teffector cells. In addition, anti-CD25-induced inactivation of Tregs in susceptible SJL/J, but not resistant B6, mice results in significantly decreased clinical disease concomitant with enhanced anti-viral CD4(+), CD8(+) and antibody responses resulting in decreased CNS viral titers. This is the first demonstration that virus-induced Treg activation regulates susceptibility to autoimmune disease differentially in susceptible and resistant strains of mice and provides a new mechanistic explanation for the etiology of infection-induced autoimmunity.

摘要

Theiler 氏鼠脑脊髓炎病毒(TMEV)诱导的脱髓鞘疾病(TMEV-IDD)是一种慢性进行性多发性硬化症的病毒诱导模型。易感 SJL/J 小鼠感染后会导致终生中枢神经系统病毒持续存在,并通过通过表位扩展激活的针对髓鞘的 T 细胞介导进行进行性自身免疫性脱髓鞘。相比之下,TMEV-IDD 抗性 C57BL/6 小鼠中快速的 CTL 反应会迅速清除病毒。我们研究了调节性 T 细胞(Tregs)的差异诱导是否会控制对 TMEV-IDD 的易感性。易感 SJL/J 感染会导致 Tregs 的快速激活和扩增,但 B6 小鼠不会,导致不利的中枢神经系统 Treg:Teffector 细胞比例。此外,在易感 SJL/J 但不是抗性 B6 小鼠中,抗 CD25 诱导的 Tregs 失活会导致临床疾病显著减少,同时增强抗病毒 CD4(+)、CD8(+) 和抗体反应,从而降低中枢神经系统病毒滴度。这是首次证明病毒诱导的 Treg 激活在易感和抗性小鼠品系中对自身免疫性疾病的易感性具有差异调节作用,并为感染诱导自身免疫的病因学提供了新的机制解释。

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