Katz E, Mitrani-Rosenbaum S, Margalith E, Ben-Bassat H
Intervirology. 1981;16(1):33-42. doi: 10.1159/000149245.
The growth of herpes simplex virus (HSV) type 1 in human lymphoid cell lines, arrested at various stages of differentiation, was studied. The synthesis of viral DNA and antigens and the production of infectious virus were followed in null, B and T leukemia-lymphoma cell lines. It was found that while "nondifferentiated" null cells and cells differentiating along the B pathway, even at very early stages of differentiation, supported HSV growth, cell lines of T origin at all stages of differentiation were generally nonpermissive. The failure of T cells to support the growth of HSV did not result from inefficient adsorption to the host cells. However, viral DNA synthesis was not detected, and a significant reduction in the ability of synthesize HSV antigens was observed. It is suggested that the block in the growth cycle of the virus occurs at a stage after adsorption of the virion to the cells, but prior to synthesis of its DNA and proteins.
对单纯疱疹病毒1型(HSV)在处于不同分化阶段的人淋巴细胞系中的生长情况进行了研究。在无特征性、B淋巴细胞和T淋巴细胞白血病 - 淋巴瘤细胞系中追踪了病毒DNA和抗原的合成以及传染性病毒的产生。结果发现,虽然“未分化”的无特征性细胞以及沿B途径分化的细胞,即使在分化的非常早期阶段,也支持HSV生长,但处于所有分化阶段的T来源细胞系通常不允许HSV生长。T细胞不能支持HSV生长并非由于对宿主细胞的吸附效率低下。然而,未检测到病毒DNA合成,并且观察到合成HSV抗原的能力显著降低。提示病毒生长周期的阻断发生在病毒粒子吸附到细胞之后,但在其DNA和蛋白质合成之前的阶段。