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从病毒感染的C57BL/6小鼠中识别被中枢神经系统浸润的CD4 + T细胞识别的泰勒氏病毒衣壳表位。

Identification of capsid epitopes of Theiler's virus recognized by CNS-infiltrating CD4+ T cells from virus-infected C57BL/6 mice.

作者信息

Kang Bongsu, Kang Hee-Kap, Kim Byung S

机构信息

Department of Microbiology-Immunology, Northwestern University Feinberg Medical School, 303 East Chicago Avenue, Chicago, IL 60611, USA.

出版信息

Virus Res. 2005 Mar;108(1-2):57-61. doi: 10.1016/j.virusres.2004.08.001.

Abstract

Intracerebral infection of Theiler's murine encephalomyelitis virus (TMEV) induces immune-mediated demyelinating disease in some mouse strains but not in others. We report here for the first time two new predominant capsid epitopes (VP4(21-40) and VP2(201-220)) recognized by CD4+ T cells from virus-infected resistant C57BL/6 mice based on IFNgamma ELISPOT assay utilizing a 20-mer peptide library covering the entire capsid proteins. Further experiments by IFNgamma ELISPOT and flow cytometry for intracellular IFNgamma production using truncated peptides indicated that the epitope regions recognized by CNS-infiltrating CD4+ T cells are VP4(25-38) and VP2(206-220), respectively. No apparent reduction in the T cell response to these viral epitopes is seen in the CNS of IL-12- and ICAM-1-deficient C57BL/6 mice compared to those in control C57BL/6 mice, suggesting that T cell response to TMEV in the CNS is largely insensitive to the absence of these proinflammatory cytokine and adhesion molecules. Therefore, these newly defined CD4+ T cell epitopes are likely to provide an important tool to investigate the role of CD4+ T cell responses in H-2b-bearing congenic strains.

摘要

泰勒氏小鼠脑脊髓炎病毒(TMEV)的脑内感染在一些小鼠品系中会引发免疫介导的脱髓鞘疾病,而在其他品系中则不会。我们在此首次报告,基于使用覆盖整个衣壳蛋白的20肽库的IFNγ ELISPOT分析,从病毒感染的抗性C57BL/6小鼠中识别出两种新的主要衣壳表位(VP4(21 - 40)和VP2(201 - 220)),它们可被CD4 + T细胞识别。使用截短肽进行的IFNγ ELISPOT和细胞内IFNγ产生的流式细胞术进一步实验表明,中枢神经系统浸润的CD4 + T细胞识别的表位区域分别为VP4(25 - 38)和VP2(206 - 220)。与对照C57BL/6小鼠相比,IL - 12和ICAM - 1缺陷的C57BL/6小鼠中枢神经系统中对这些病毒表位的T细胞反应没有明显降低,这表明中枢神经系统中TMEV的T细胞反应在很大程度上对这些促炎细胞因子和黏附分子的缺失不敏感。因此,这些新定义的CD4 + T细胞表位可能为研究CD4 + T细胞反应在携带H - 2b的同源品系中的作用提供重要工具。

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