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本文引用的文献

1
A critical role for virus-specific CD8(+) CTLs in protection from Theiler's virus-induced demyelination in disease-susceptible SJL mice.病毒特异性 CD8(+) CTLs 在抵抗 SJL 易感小鼠中由 Theiler 病毒引起的脱髓鞘疾病中的关键作用。
Virology. 2010 Jun 20;402(1):102-11. doi: 10.1016/j.virol.2010.02.031. Epub 2010 Apr 8.
2
Antiviral immune responses: triggers of or triggered by autoimmunity?抗病毒免疫反应:自身免疫的触发因素还是由自身免疫引发?
Nat Rev Immunol. 2009 Apr;9(4):246-58. doi: 10.1038/nri2527.
3
Regulatory T cells promote early influx of CD8+ T cells in the lungs of respiratory syncytial virus-infected mice and diminish immunodominance disparities.调节性T细胞促进呼吸道合胞病毒感染小鼠肺部CD8 + T细胞的早期流入,并减少免疫优势差异。
J Virol. 2009 Apr;83(7):3019-28. doi: 10.1128/JVI.00036-09. Epub 2009 Jan 19.
4
Acute hemorrhagic demyelination in a murine model of multiple sclerosis.多发性硬化症小鼠模型中的急性出血性脱髓鞘病变
J Neuroinflammation. 2008 Jul 7;5:31. doi: 10.1186/1742-2094-5-31.
5
The genetics of multiple sclerosis: SNPs to pathways to pathogenesis.多发性硬化症的遗传学:从单核苷酸多态性到发病机制的途径
Nat Rev Genet. 2008 Jul;9(7):516-26. doi: 10.1038/nrg2395. Epub 2008 Jun 10.
6
In vitro-generated antigen-specific CD4+ CD25+ Foxp3+ regulatory T cells control the severity of herpes simplex virus-induced ocular immunoinflammatory lesions.体外产生的抗原特异性CD4+CD25+Foxp3+调节性T细胞可控制单纯疱疹病毒诱导的眼部免疫炎性病变的严重程度。
J Virol. 2008 Jul;82(14):6838-51. doi: 10.1128/JVI.00697-08. Epub 2008 May 14.
7
Expansion of hepatitis C-specific CD4+CD25+ regulatory T cells after viral clearance: a mechanism to limit collateral damage?病毒清除后丙型肝炎特异性CD4+CD25+调节性T细胞的扩增:一种限制附带损害的机制?
J Allergy Clin Immunol. 2008 May;121(5):1277-1284.e3. doi: 10.1016/j.jaci.2008.01.070. Epub 2008 Mar 19.
8
Identification and in vitro expansion of functional antigen-specific CD25+ FoxP3+ regulatory T cells in hepatitis C virus infection.丙型肝炎病毒感染中功能性抗原特异性CD25 + FoxP3 +调节性T细胞的鉴定及体外扩增
J Virol. 2008 May;82(10):5043-53. doi: 10.1128/JVI.01548-07. Epub 2008 Mar 12.
9
Foxp3+ regulatory T cells in the control of experimental CNS autoimmune disease.Foxp3 +调节性T细胞对实验性中枢神经系统自身免疫性疾病的控制作用
J Neuroimmunol. 2008 Jan;193(1-2):1-11. doi: 10.1016/j.jneuroim.2007.11.016.
10
Risk alleles for multiple sclerosis identified by a genomewide study.一项全基因组研究确定的多发性硬化症风险等位基因。
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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.

DOI:10.1016/j.jaut.2010.12.005
PMID:21273044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3046315/
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。