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初始与活化的泰勒氏病毒表位特异性CD8 + 细胞毒性T细胞在耐受性诱导中的不同结果。

Differential outcome of tolerance induction in naive versus activated Theiler's virus epitope-specific CD8+ cytotoxic T cells.

作者信息

Getts Meghann Teague, Kim Byung S, Miller Stephen D

机构信息

Department of Microbiology and Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA.

出版信息

J Virol. 2007 Jun;81(12):6584-93. doi: 10.1128/JVI.00008-07. Epub 2007 Apr 11.

DOI:10.1128/JVI.00008-07
PMID:17428853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1900084/
Abstract

Tolerance induced by the intravenous injection of peptide-pulsed, ethylene carbodiimide (ECDI)-fixed splenic antigen-presenting cells (Ag-SP) is a safe and effective method of inducing specific unresponsiveness in CD4+ T cells for the prevention and treatment of a variety of autoimmune diseases. We determined whether Ag-SP tolerance could also be used to tolerize CD8+ T cells. We show in the Theiler's murine encephalomyelitis virus (TMEV)-induced demyelinating disease model of multiple sclerosis that CD8+ T cells specific for both dominant and subdominant epitopes can be rendered tolerant. Interestingly, although virus clearance was delayed, lack of the virus-specific cytotoxic T-lymphocyte response did not result in the conversion of normally TMEV-resistant C57BL/6 mice to a susceptible phenotype. Importantly, we found that Ag-SP tolerance may not be a practical treatment for human diseases in which CD8+ T cells play a major role in pathogenesis, as tolerance induction in mice previously infected with TMEV led to a severe, often fatal reaction.

摘要

通过静脉注射肽脉冲、碳二亚胺(ECDI)固定的脾抗原呈递细胞(Ag-SP)诱导的耐受性是一种安全有效的方法,可诱导CD4+ T细胞产生特异性无反应性,用于预防和治疗多种自身免疫性疾病。我们确定了Ag-SP耐受性是否也可用于使CD8+ T细胞产生耐受性。我们在多发性硬化症的泰勒氏鼠脑脊髓炎病毒(TMEV)诱导的脱髓鞘疾病模型中表明,对显性和隐性表位均特异的CD8+ T细胞可产生耐受性。有趣的是,尽管病毒清除延迟,但缺乏病毒特异性细胞毒性T淋巴细胞反应并未导致正常对TMEV有抗性的C57BL/6小鼠转变为易感表型。重要的是,我们发现Ag-SP耐受性可能不是治疗CD8+ T细胞在发病机制中起主要作用的人类疾病的实用方法,因为在先前感染TMEV的小鼠中诱导耐受性会导致严重的、通常是致命的反应。

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