Yasukawa M, Hatta N, Sada E, Inoue Y, Murakami T, Onji M, Fujita S
First Department of Internal Medicine, Ehime University School of Medicine, Shigenobu, Japan.
J Gen Virol. 1996 Dec;77 ( Pt 12):3103-6. doi: 10.1099/0022-1317-77-12-3103.
To evaluate the role of the OKT4 epitope in human herpesvirus 7 (HHV-7) infection, we studied the susceptibility to HHV-7 infection of CD4+ T cells isolated from two individuals with OKT4 epitope deficiency. HHV-7-infected OKT4-Leu3a+ T cells exhibited the characteristic cytopathic effect, reactivity with HHV-7-seropositive serum by immunofluorescence and down-modulation of surface CD4 in a manner similar to HHV-7-infected OKT4+Leu3a+ T cells. A semiquantitative PCR revealed that the amounts of HHV-7 replicated in OKT4+Leu3a+ T cells and OKT4-Leu3a+ T cells were not significantly different. Although it has been reported that OKT4 monoclonal antibody efficiently inhibits HHV-7 infection, the present study demonstrated that the interaction of HHV-7 with CD4+ T cells does not require participation of the epitope defined by OKT4 monoclonal antibody.
为评估OKT4表位在人疱疹病毒7型(HHV-7)感染中的作用,我们研究了从两名存在OKT4表位缺陷的个体中分离出的CD4⁺ T细胞对HHV-7感染的易感性。被HHV-7感染的OKT4-Leu3a⁺ T细胞表现出特征性细胞病变效应,通过免疫荧光法显示与HHV-7血清阳性血清有反应性,并且表面CD4呈下调状态,其方式类似于被HHV-7感染的OKT4⁺Leu3a⁺ T细胞。半定量PCR显示,在OKT4⁺Leu3a⁺ T细胞和OKT4-Leu3a⁺ T细胞中复制的HHV-7量没有显著差异。尽管已有报道称OKT4单克隆抗体可有效抑制HHV-7感染,但本研究表明,HHV-7与CD4⁺ T细胞的相互作用并不需要OKT4单克隆抗体所定义的表位参与。