首页> 美国卫生研究院文献>Journal of Virology >Epstein-Barr virus-specific cytotoxic T-cell recognition of transfectants expressing the virus-coded latent membrane protein LMP.
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Epstein-Barr virus-specific cytotoxic T-cell recognition of transfectants expressing the virus-coded latent membrane protein LMP.

机译:表达病毒编码潜伏膜蛋白LMP的转染子的爱泼斯坦-巴尔病毒特异的细胞毒性T细胞识别。

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摘要

Cytotoxic T cells from Epstein-Barr virus (EBV)-immune individuals specifically kill EBV-transformed B cells from HLA class I antigen-matched donors even though the latently infected cells express only a restricted set of virus genes. The virus-induced target antigens recognized by these immune T cells have not been identified. In our experiments, EBV DNA sequences encoding the virus latent gene products Epstein-Barr nuclear antigen (EBNA)1, EBNA 2, and EBNA-LP and the latent membrane protein (LMP) were individually expressed in a virus-negative human B-lymphoma cell line, Louckes. Transfected clones expressing LMP were killed by EBV-specific cytotoxic T-cell preparations from each of three virus-immune donors HLA matched with Louckes through HLA-A2, B44 antigens; control transfectants or clones expressing one of the EBNA proteins were not recognized. Expression of LMP in a second virus-negative B-cell line, BL41, sensitized these cells to EBV-specific cytolysis restricted through the HLA-A11 antigen. To distinguish between the viral protein and an induced human B-cell activation antigen as the target for T-cell recognition, LMP was then expressed in a murine mastocytoma cell line, P815-A11-restricted human T cells. The LMP-expressing P815-A11 transfectants were susceptible to lysis by EBV-specific cytotoxic T cells from three HLA-A11-positive individuals. Both Louckes and P815-A11 cells were also transfected with constructs capable of encoding a truncated form of LMP (Tr-LMP) which lacks the N-terminal 128 amino acids of the full-length protein. Tr-LMP-expressing transfectants were not recognized by the above T-cell preparations. The results suggest that LMP, and, in particular, epitopes derived from the N-terminal region of the protein, provides one of the target antigens for the EBV-induced human cytotoxic T-cell response.
机译:来自爱泼斯坦-巴尔病毒(EBV)免疫个体的细胞毒性T细胞可特异性杀死HLA I类抗原匹配供体的EBV转化B细胞,即使潜伏感染的细胞仅表达有限的一组病毒基因。这些免疫T细胞识别的病毒诱导的靶抗原尚未鉴定。在我们的实验中,编码病毒潜伏基因产物爱泼斯坦-巴尔核抗原(EBNA)1,EBNA 2和EBNA-LP的EBV DNA序列和潜伏膜蛋白(LMP)在病毒阴性的人类B淋巴瘤中单独表达细胞系,Louckes。转染了表达LMP的克隆被EBV特异性细胞毒性T细胞制剂杀死,该制剂来​​自三个通过HLA-A2,B44抗原与Louckes配对的HLA病毒免疫供体。不能识别表达EBNA蛋白之一的对照转染子或克隆。 LMP在第二种病毒阴性B细胞系BL41中的表达使这些细胞对受HLA-A11抗原限制的EBV特异性细胞溶解敏感。为了区分病毒蛋白和诱导的人B细胞活化抗原作为T细胞识别的靶标,然后在鼠肥大细胞瘤细胞系P815-A11限制的人T细胞中表达LMP。表达LMP的P815-A11转染子易受来自三个HLA-A11阳性个体的EBV特异性细胞毒性T细胞裂解的影响。 Louckes细胞和P815-A11细胞也都用能够编码截短形式的LMP(Tr-LMP)的构建体转染,LMP(Tr-LMP)缺少全长蛋白质的N端128个氨基酸。上述T细胞制品不能识别表达Tr-LMP的转染子。结果表明,LMP,特别是衍生自蛋白质N端区域的表位,为EBV诱导的人细胞毒性T细胞反应提供了一种靶抗原。

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