Duff R, Rapp F
J Virol. 1971 Oct;8(4):469-77. doi: 10.1128/JVI.8.4.469-477.1971.
An in vitro method which led to the transformation of hamster embryo fibroblasts after exposure to herpes simplex virus type 2 (HSV-2) inactivated with ultraviolet irradiation is described. The transformed cells (333-8-9) produced tumors when inoculated into newborn Syrian hamsters but not when injected into weanling Syrian hamsters of the same LSH inbred strain. However, after one in vivo passage, the 333-8-9 cells became highly oncogenic in weanling hamsters. No infectious virus was recovered from these cells. Herpes simplex virus antigens were detected in the transformed cells by the indirect immunofluorescence technique. Sera from tumor-bearing hamsters contained antibody with highly specific neutralizing activity against HSV-2. These studies indicate the continued involvement of the HSV-2 genome in an oncogenic cell line.
本文描述了一种体外方法,该方法可使仓鼠胚胎成纤维细胞在暴露于经紫外线照射灭活的2型单纯疱疹病毒(HSV-2)后发生转化。将转化后的细胞(333-8-9)接种到新生叙利亚仓鼠体内时会产生肿瘤,但注射到同一LSH近交系的断奶叙利亚仓鼠体内时则不会。然而,经过一次体内传代后,333-8-9细胞在断奶仓鼠中变得具有高度致癌性。从这些细胞中未检测到传染性病毒。通过间接免疫荧光技术在转化细胞中检测到单纯疱疹病毒抗原。荷瘤仓鼠的血清中含有对HSV-2具有高度特异性中和活性的抗体。这些研究表明HSV-2基因组持续参与了一个致癌细胞系的形成。