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预防性给予小鼠γ干扰素治疗后,感染小鼠巨细胞病毒的小鼠死亡率降低。

Reduced mortality in murine cytomegalovirus infected mice following prophylactic murine interferon-gamma treatment.

作者信息

Fennie E H, Lie Y S, Low M A, Gribling P, Anderson K P

机构信息

Department of Pharmacological Sciences, Genentech, Inc., South San Francisco, CA 94080.

出版信息

Antiviral Res. 1988 Nov;10(1-3):27-39. doi: 10.1016/0166-3542(88)90012-5.

Abstract

Efficacy of recombinant DNA-derived murine IFN-gamma was investigated in a murine model of cytomegalovirus infection. Treatment of 3-week-old Swiss Webster mice with murine IFN-gamma prior to infection with murine cytomegalovirus (MCMV) significantly reduced mortality due to MCMV infection. Efficacy was dose-dependent and was observed using either intraperitoneal or intramuscular injection as the route of administration. Two doses, one at 24 h and one at 4 h prior to MCMV infection, were required for optimum efficacy, and doses administered after MCMV infection had no apparent effect. Reduced infectious MCMV titers were observed in critical organs of IFN-gamma treated mice and histopathologic lesions induced by MCMV infection were in general less severe and resolved sooner than lesions in untreated mice. Results in this murine model of cytomegalovirus infection suggest that IFN-gamma treatment may be useful as prophylactic therapy for human cytomegalovirus infections when a high probability of exposure to the virus exists and consequences of infection may be severe.

摘要

在巨细胞病毒感染的小鼠模型中研究了重组DNA衍生的鼠干扰素-γ的疗效。在用鼠巨细胞病毒(MCMV)感染前,用鼠干扰素-γ治疗3周龄的瑞士韦伯斯特小鼠,可显著降低因MCMV感染导致的死亡率。疗效呈剂量依赖性,且通过腹腔注射或肌肉注射作为给药途径均观察到了该疗效。为达到最佳疗效,需要在MCMV感染前24小时和4小时各给药一次,MCMV感染后给药则无明显效果。在接受干扰素-γ治疗的小鼠的关键器官中观察到感染性MCMV滴度降低,并且MCMV感染诱导的组织病理学损伤总体上比未治疗小鼠的损伤更轻,且愈合更快。在这个巨细胞病毒感染的小鼠模型中的结果表明,当存在高暴露于该病毒的可能性且感染后果可能很严重时,干扰素-γ治疗可能作为人类巨细胞病毒感染的预防性治疗手段。

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