Jordan M C, Takagi J L, Stevens J G
J Infect Dis. 1982 May;145(5):699-705. doi: 10.1093/infdis/145.2.699.
Many cytomegalovirus (CMV) infections result from activation of virus previously latent in the host. Murine models of latent CMV infection have been developed in which latent virus can be activated in vivo by immunosuppression or by coculture of splenic lymphocytes in vitro. In the present study, latent murine CMV (MCMV) could be activated from lymphocytes of mice regardless of genetic strain, age at time of virus inoculation, or use of syngeneic or allogeneic fibroblasts for coculture. After intraperitoneal inoculation, virulent virus was activated from lymphocytes more often than attenuated MCMV (69% vs. 20% of lymphocyte cocultures were positive, respectively). Latent MCMV was not detected in lymphocytes after subcutaneous inoculation of weanling mice but could be activated from mice infected subcutaneously as newborns. The absence of latent infection in the lymphocytes of the mice that had been inoculated as weanlings was due to lack of virus replication in the spleen during acute infection.
许多巨细胞病毒(CMV)感染是由宿主中先前潜伏的病毒激活所致。已经建立了潜伏性CMV感染的小鼠模型,其中潜伏病毒可通过免疫抑制或体外脾淋巴细胞共培养在体内被激活。在本研究中,无论遗传品系、接种病毒时的年龄,或使用同基因或异基因成纤维细胞进行共培养,潜伏性小鼠巨细胞病毒(MCMV)均可从小鼠淋巴细胞中被激活。腹腔接种后,强毒株病毒比减毒MCMV更常从淋巴细胞中被激活(淋巴细胞共培养阳性率分别为69%和20%)。对断奶小鼠进行皮下接种后,淋巴细胞中未检测到潜伏性MCMV,但可从新生时即被皮下感染的小鼠中激活潜伏性MCMV。断奶时接种的小鼠淋巴细胞中无潜伏感染,是由于急性感染期间脾脏中缺乏病毒复制。