Yasukawa M, Inoue Y, Kimura N, Fujita S
First Department of Internal Medicine, Ehime University School of Medicine, Japan.
J Virol. 1995 Dec;69(12):8114-7. doi: 10.1128/JVI.69.12.8114-8117.1995.
Herpesvirus saimiri (HVS) has recently been shown to immortalize human CD4+ and CD8+ T cells expressing T-cell receptor alpha beta (TCR-alpha beta) with the maintenance of their original phenotypes and functional properties. However, the immortalization of human T cells expressing TCR-gamma delta by HVS has not been successful. Here we report that HVS can also infect and immortalize human T cells expressing TCR-gamma delta. Two human TCR-gamma delta+ T-cell clones, which continuously proliferated in interleukin-2-containing culture medium without any exogenous stimulation or addition of feeder cells for more than 8 months, were established by HVS infection. Morphologically, the HVS-transformed TCR-gamma delta+ T-cell clones were granular lymphocytes which exhibited wide-range HLA-unrestricted cytotoxicity as untransformed TCR-gamma delta+ T cells. Their phenotypes and cytotoxic activities were not altered during long-term culture. The immortalization of human TCR-gamma delta+ T cells by HVS infection would be useful for functional analysis of this lymphocyte population, which is believed to play an important role in protection against various infectious diseases.
最近研究表明,赛米利疱疹病毒(HVS)可使表达αβ型T细胞受体(TCR-αβ)的人CD4⁺和CD8⁺T细胞永生化,并维持其原始表型和功能特性。然而,HVS未能成功使表达γδ型T细胞受体(TCR-γδ)的人T细胞永生化。在此,我们报告HVS也可感染并使表达TCR-γδ的人T细胞永生化。通过HVS感染建立了两个人TCR-γδ⁺T细胞克隆,它们在含白细胞介素-2的培养基中持续增殖超过8个月,无需任何外源性刺激或添加饲养细胞。形态学上,HVS转化的TCR-γδ⁺T细胞克隆为颗粒淋巴细胞,与未转化的TCR-γδ⁺T细胞一样,表现出广泛的HLA非限制性细胞毒性。在长期培养过程中,它们的表型和细胞毒性活性未发生改变。通过HVS感染使人类TCR-γδ⁺T细胞永生化,将有助于对这一淋巴细胞群体进行功能分析,据信该群体在抵御各种传染病中发挥着重要作用。