Lawman M J, Rouse B T, Courtney R J, Walker R D
Infect Immun. 1980 Jan;27(1):133-9. doi: 10.1128/iai.27.1.133-139.1980.
The conditions required for the induction of both primary cytotoxic T lymphocytes (CTL) in vivo and secondary CTL in vitro against herpes simplex virus type 1 (HSV-1)-infected cells were defined. Primary CTL responses occurred only in mice exposed to infectious HSV-1. These responses, which were shown to be mediated by T lymphocytes, peaked at 1 week and had disappeared by 2 weeks after infection. The level of primary cytotoxicity was enhanced by treatment of mice with cyclophosphamide before infection. Secondary in vitro CTL responses were more pronounced and were induced by some forms of inactivated virus as well as by infectious HSV-1. Thus, both ultraviolet light- and glutaraldehyde-inactivated preparations of HSV-1 induced CTL, but heat-inactivated and detergent-extracted antigens failed to do so. The reasons for the differing efficiency of infectious and noninfectious HSV-1 for induction of CTL are discussed.
确定了在体内诱导针对1型单纯疱疹病毒(HSV-1)感染细胞的原发性细胞毒性T淋巴细胞(CTL)以及在体外诱导继发性CTL所需的条件。原发性CTL反应仅在暴露于传染性HSV-1的小鼠中出现。这些反应被证明是由T淋巴细胞介导的,在感染后1周达到峰值,并在2周后消失。感染前用环磷酰胺治疗小鼠可增强原发性细胞毒性水平。继发性体外CTL反应更为明显,可由某些形式的灭活病毒以及传染性HSV-1诱导产生。因此,HSV-1的紫外线和戊二醛灭活制剂均可诱导CTL,但热灭活和去污剂提取的抗原则不能。文中讨论了传染性和非传染性HSV-1诱导CTL效率不同的原因。