Yoshiyama H, Shimizu N, Takada K
Department of Virology and Parasitology, Yamaguchi University School of Medicine, Japan.
EMBO J. 1995 Aug 1;14(15):3706-11. doi: 10.1002/j.1460-2075.1995.tb00040.x.
The growth transforming potential of Epstein-Barr virus (EBV) for Burkitt's lymphoma and nasopharyngeal carcinoma is now extended to other neoplasia, such as Hodgkin's disease, peripheral T-cell tumor and gastric cancer. We have generated an EBV recombinant with a selectable marker at the viral thymidine kinase locus. Recombinant EBV was successfully infected into a human T-cell line, MT-2. Following incubation in the selective medium, drug resistant MT-2 cell clones were isolated and proved to be infected with recombinant EBV. EBV-infected MT-2 cell clones expressed EBNA 1 and LMP 1 and very little of EBNA 2, showing the BamHI F promoter-driven latency II form of infection, which is seen in non-B-cell tumors. This is the first report of in vitro generation of latency II type EBV infection. The present system of persistent EBV infection in T cells should be a good model for investigating the pathogenic role of EBV in non-B-cell tumors.
爱泼斯坦-巴尔病毒(EBV)对伯基特淋巴瘤和鼻咽癌的生长转化潜能现已扩展到其他肿瘤,如霍奇金病、外周T细胞肿瘤和胃癌。我们在病毒胸苷激酶基因座处构建了带有选择标记的EBV重组体。重组EBV成功感染了人T细胞系MT-2。在选择性培养基中培养后,分离出耐药的MT-2细胞克隆,并证明其感染了重组EBV。EBV感染的MT-2细胞克隆表达EBNA 1和LMP 1,而EBNA 2表达很少,呈现出BamHI F启动子驱动的潜伏II型感染形式,这种形式在非B细胞肿瘤中可见。这是关于体外产生潜伏II型EBV感染的首次报道。目前T细胞中持续性EBV感染的系统应是研究EBV在非B细胞肿瘤中致病作用较好的模型。