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泰勒病毒VP1蛋白上的淋巴细胞识别元件。

Lymphocyte recognition elements on the VP1 protein of Theiler's virus.

作者信息

Usherwood E J, Johnston I C, Lovelidge L J, Tonks P, Nash A A

机构信息

Department of Pathology, University of Cambridge, UK.

出版信息

Immunology. 1995 Jun;85(2):190-7.

Abstract

Theiler's virus is a murine picornavirus that persists in the central nervous system in susceptible mouse strains, and gives rise to immune mediated demyelinating disease. Antiviral CD4 T cells are necessary to protect from overwhelming virus replication in the acute phase of the disease, and are thought to act by stimulating the antibody response. The present study used overlapping synthetic peptides to map the location of epitopes recognized by CD4 T cells. One T-cell epitope was identified between amino acids 33-47 of VP1, which was recognized by virus-reactive T cells. 'Cryptic' epitopes were also present within VP1 at positions 153-167, 166-180, 225-239 and 233-247. A linear B-cell epitope was identified in the C-terminal region 225-276. Immunization of CBA mice with inactivated virus, but not peptides containing VP1 B- or T-cell epitopes, reduced the virus titre in the CNS in the acute phase of the disease.

摘要

泰勒氏病毒是一种鼠微小核糖核酸病毒,可在易感小鼠品系的中枢神经系统中持续存在,并引发免疫介导的脱髓鞘疾病。抗病毒CD4 T细胞对于在疾病急性期防止病毒大量复制至关重要,并且被认为通过刺激抗体反应发挥作用。本研究使用重叠合成肽来定位CD4 T细胞识别的表位位置。在病毒反应性T细胞识别的VP1的33-47位氨基酸之间鉴定出一个T细胞表位。“隐蔽”表位也存在于VP1的153-167、166-180、225-239和233-247位。在C末端区域225-276中鉴定出一个线性B细胞表位。用灭活病毒免疫CBA小鼠,但不用含有VP1 B或T细胞表位的肽免疫,可在疾病急性期降低中枢神经系统中的病毒滴度。

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