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小鼠肝炎病毒的JHM株可诱导一种刺突蛋白特异性的Db限制性细胞毒性T细胞反应。

The JHM strain of mouse hepatitis virus induces a spike protein-specific Db-restricted cytotoxic T cell response.

作者信息

Bergmann C C, Yao Q, Lin M, 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 Gen Virol. 1996 Feb;77 ( Pt 2 ):315-25. doi: 10.1099/0022-1317-77-2-315.

Abstract

Cytotoxic T lymphocyte (CTL) activity specific for mouse hepatitis virus (MHV) JHM strain (JHMV or MHV-4) was examined using in vitro stimulated spleen cells derived from immunized C57BL/6 (H-2b) mice. Target cells infected with JHMV were specifically recognized; however, analysis of target cells expressing the virus structural proteins via recombinant vaccinia viruses showed no recognition of the viral nucleocapsid (N), membrane (M), small membrane (sM) or haemagglutinin-esterase (HE) proteins. Only target cells expressing the virus spike (S) protein were recognized. Furthermore, the majority of CTL activity was restricted to target cells expressing the MHC class I Db molecules. Analysis of truncations and deletions of the S protein expressed by recombinant vaccinia viruses and peptide coated targets identified a single antigenic epitope, aa 510-518, conforming to the Db binding motif. These amino acids are contained within a domain deleted from a number of strains of mouse hepatitis virus, suggesting a role for immune pressure. To determine the potential for CTL specific for an epitope(s) within a non-structural protein, 24 CTL lines were established and characterized. No evidence for the induction of non-specific CTL activity or virus-specific CTL restricted to an epitope in a non-structural protein was obtained. These data indicate that the predominant CTL activity in JHMV-infected C57BL/6 mice is Db restricted and specific for a single epitope contained within aa 510-518 of the S protein.

摘要

利用来自免疫的C57BL/6(H-2b)小鼠的体外刺激脾细胞,检测了对小鼠肝炎病毒(MHV)JHM株(JHMV或MHV-4)具有特异性的细胞毒性T淋巴细胞(CTL)活性。感染JHMV的靶细胞被特异性识别;然而,通过重组痘苗病毒表达病毒结构蛋白的靶细胞分析显示,未识别出病毒核衣壳(N)、膜(M)、小膜(sM)或血凝素酯酶(HE)蛋白。仅识别表达病毒刺突(S)蛋白的靶细胞。此外,大多数CTL活性仅限于表达MHC I类Db分子的靶细胞。对重组痘苗病毒表达的S蛋白截短和缺失以及肽包被靶标的分析确定了一个单一抗原表位,即氨基酸510-518,符合Db结合基序。这些氨基酸包含在许多小鼠肝炎病毒株缺失的一个结构域内,提示免疫压力的作用。为了确定针对非结构蛋白内一个或多个表位的CTL潜力,建立并鉴定了24个CTL系。未获得诱导非特异性CTL活性或局限于非结构蛋白中一个表位的病毒特异性CTL的证据。这些数据表明,在感染JHMV的C57BL/6小鼠中,主要的CTL活性受Db限制,且对S蛋白氨基酸510-518内包含的单一表位具有特异性。

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