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H-2 L(d) 限制性细胞毒性T淋巴细胞对小鼠肝炎病毒核衣壳蛋白反应的特异性

Specificity of the H-2 L(d)-restricted cytotoxic T-lymphocyte response to the mouse hepatitis virus nucleocapsid protein.

作者信息

Bergmann C C, Stohlman S A

机构信息

Department of Neurology, University of Southern California School of Medicine, Los Angeles 90033, USA.

出版信息

J Virol. 1996 May;70(5):3252-7. doi: 10.1128/JVI.70.5.3252-3257.1996.

Abstract

Cytotoxic T lymphocytes provide protection against persistent infection of the central nervous system by the JHM strain of mouse hepatitis virus. In BALB/c (H-2d) mice, the dominant response is directed against an Ld-restricted peptide in the nucleocapsid protein (APTAGAFFF). Characterization of the fine specificity of this response revealed that the predicted anchor residues at positions 2 and 9 were the most critical for class I binding. Amino acids at positions 7 and 8 were identified as T-cell receptor contact residues. Virus-induced cytotoxic T lymphocytes to other Ld motif-containing nucleocapsid peptides were not detected, despite the identification of two epitopes with reduced Ld affinity. These data suggest that mutations within four residues of the dominant epitope could contribute to the persistence of the JHM strain of mouse hepatitis virus.

摘要

细胞毒性T淋巴细胞可提供针对小鼠肝炎病毒JHM株对中枢神经系统持续感染的保护作用。在BALB/c(H-2d)小鼠中,主要反应针对核衣壳蛋白中的一种Ld限制性肽(APTAGAFFF)。对该反应精细特异性的表征显示,第2和9位预测的锚定残基对于I类结合最为关键。第7和8位的氨基酸被确定为T细胞受体接触残基。尽管鉴定出两个与Ld亲和力降低的表位,但未检测到针对其他含Ld基序的核衣壳肽的病毒诱导的细胞毒性T淋巴细胞。这些数据表明,主要表位四个残基内的突变可能导致小鼠肝炎病毒JHM株的持续存在。

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