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对EB病毒的B型特异性和交叉反应性细胞毒性T淋巴细胞反应的鉴定。

Identification of type B-specific and cross-reactive cytotoxic T-lymphocyte responses to Epstein-Barr virus.

作者信息

Kerr B M, Kienzle N, Burrows J M, Cross S, Silins S L, Buck M, Benson E M, Coupar B, Moss D J, Sculley T B

机构信息

Queensland Institute of Medical Research, The Bancroft Centre, Brisbane, Australia.

出版信息

J Virol. 1996 Dec;70(12):8858-64. doi: 10.1128/JVI.70.12.8858-8864.1996.

Abstract

Persistent Epstein-Barr virus (EBV) infection is primarily controlled by HLA class I-restricted memory cytotoxic T-cell (CTL) responses which can be reactivated in vitro by stimulation of peripheral blood lymphocytes with autologous lymphoblastoid cell lines. During an investigation of a donor infected by both type A and type B EBV, CTL specific for type B EBV were isolated. The CTL were found to recognize an epitope encoded by the EBNA-6B gene. The minimal epitope sequence was identified as QNGALAINTF, corresponding to residues 213 to 222 in the EBNA-6B protein, and presentation of this epitope was shown to be via HLA B62 (B15). This is the first report of the characterization of an epitope that is EBV type B specific. CTL recognizing sequences common to type A and type B EBV were identified as well. A cross-reactive epitope recognized by these CTL was encoded within the EBNA-6 gene of both type A and type B. This minimal sequence for this epitope was LLDFVRFMGV (residues 284 to 293 in both types), and the epitope was restricted through HLA A*0201. This second epitope sequence overlaps with a published EBV B44-restricted epitope (EENLLDFVRF). The implications of these findings are discussed with respect to the design and efficacy of epitope-based vaccines.

摘要

持续性EB病毒(EBV)感染主要由HLA I类限制性记忆细胞毒性T细胞(CTL)反应控制,通过用自体淋巴母细胞系刺激外周血淋巴细胞可在体外重新激活这种反应。在对一名同时感染A和B型EBV的供体进行调查期间,分离出了针对B型EBV的CTL。发现这些CTL识别由EBNA - 6B基因编码的一个表位。最小表位序列被确定为QNGALAINTF,对应于EBNA - 6B蛋白中的第213至222位氨基酸残基,并且该表位的呈递是通过HLA B62(B15)。这是关于B型EBV特异性表位特征描述的首次报告。也鉴定出了识别A和B型EBV共有序列的CTL。这些CTL识别的一个交叉反应性表位在A和B型的EBNA - 6基因内编码。该表位的这个最小序列是LLDFVRFMGV(两种类型中均为第284至293位氨基酸残基),并且该表位受HLA A*0201限制。第二个表位序列与已发表的EBV B44限制性表位(EENLLDFVRF)重叠。就基于表位的疫苗的设计和功效对这些发现的意义进行了讨论。

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