Hügin A W, Flexner C, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institute of Health, Bethesda, Maryland 20892.
Cell Immunol. 1993 Dec;152(2):499-509. doi: 10.1006/cimm.1993.1307.
Recombinant vaccinia viruses that express the human or mouse IL-2 gene are rapidly eliminated from immunoincompetent nude mice whereas control viruses cause lethal infections. To understand the role that virus-encoded IL-2 plays in attenuation, we investigated the mechanism of virus elimination from nude mice. Survival correlated with accelerated clearance of the virus. Treatment of infected mice with antibodies to eliminate NK cells or to neutralize interferon-gamma suggested that both are involved in the elimination of IL-2-producing virus. However, lytic activity of NK cells was not necessary as shown by studies with beige mice. Coinfection with IL-2-expressing and control virus resulted in lethal infection of nude mice, indicating the absence of significant systemic immunity. Focally acting immunopotentiating and chemotactic activities of virus-encoded IL-2 and host-derived interferon-gamma seem to confer protection in this novel approach to virus attenuation.
表达人或小鼠白细胞介素-2(IL-2)基因的重组痘苗病毒在免疫功能不全的裸鼠中会迅速被清除,而对照病毒则会引发致命感染。为了了解病毒编码的IL-2在减毒过程中所起的作用,我们研究了裸鼠体内病毒清除的机制。存活情况与病毒清除加速相关。用抗体处理感染小鼠以清除自然杀伤细胞(NK细胞)或中和γ干扰素,结果表明二者都参与了产生IL-2病毒的清除。然而,正如对米色小鼠的研究所显示的,NK细胞的裂解活性并非必需。同时感染表达IL-2的病毒和对照病毒会导致裸鼠致命感染,这表明不存在显著的全身免疫。病毒编码的IL-2和宿主来源的γ干扰素的局部免疫增强和趋化活性似乎在这种新型病毒减毒方法中提供了保护作用。