Shanley J D, Pesanti E L, Nugent K M
J Infect Dis. 1982 Sep;146(3):388-96. doi: 10.1093/infdis/146.3.388.
Virus replication and interstitial pneumonia were studied in BALB/c mice inoculated intranasally with murine cytomegalovirus (MCMV). In normal mice MCMV replicated in lung tissue but did not produce any consistent histologic abnormalities through day 21. The addition of a single dose of cyclophosphamide (0.20 mg/g) 24 hr after virus inoculation resulted in a slight increase in lung virus titers on day 10. No histologic abnormalities were noted before day 10. However, 22 or 32 virus-infected mice treated with a single dose of cyclophosphamide but only two of 26 simultaneously mock-infected, cyclophosphamide-treated mice developed severe interstitial pneumonia 10-14 days after inoculation. In contrast, animals given cyclophosphamide (0.05 mg/g) every five days after the initial dose developed a 10-fold increase in lung virus titer, but interstitial pneumonia was not observed. These data suggest that the interstitial pneumonitis seen with MCMV pulmonary infection may be immunologically mediated rather than the result of direct viral damage to the lung.
对经鼻接种鼠巨细胞病毒(MCMV)的BALB/c小鼠的病毒复制和间质性肺炎进行了研究。在正常小鼠中,MCMV在肺组织中复制,但直到第21天未产生任何一致的组织学异常。在病毒接种后24小时给予单剂量环磷酰胺(0.20mg/g)导致第10天肺病毒滴度略有增加。在第10天之前未观察到组织学异常。然而,22只或32只接受单剂量环磷酰胺治疗的病毒感染小鼠中,只有2只同时接受假感染、环磷酰胺治疗的26只小鼠中的2只在接种后10 - 14天出现严重间质性肺炎。相比之下,初始剂量后每五天给予环磷酰胺(0.05mg/g)的动物肺病毒滴度增加了10倍,但未观察到间质性肺炎。这些数据表明,MCMV肺部感染所见的间质性肺炎可能是免疫介导的,而非病毒直接损伤肺的结果。