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用阿昔洛韦和干扰素治疗小鼠巨细胞病毒肺炎。

Treatment of murine cytomegalovirus pneumonia with acyclovir and interferon.

作者信息

Rose R M, Crumpacker C, Waner J L, Brain J D

出版信息

Am Rev Respir Dis. 1983 Feb;127(2):198-203. doi: 10.1164/arrd.1983.127.2.198.

Abstract

A murine model of lethal cytomegalovirus pneumonia following intratracheal inoculation of normal mice was used to study the effects of antiviral therapy with acyclovir (ACV) and interferon (IF), alone and in combination. Five hundred units of fibroblast IF administered intraperitoneally the day prior to infection and 100 mg/kg/day ACV administered intraperitoneally for 7 days beginning within 3 h of infection were both highly effective in preventing mortality. Compared to the condition of untreated animals, each drug reduced viral titers in lung homogenates of the treated animals 7 days after infection. However ACV, unlike IF, diminished viral growth in the lung at 14 days, prevented viral dissemination to spleens and salivary glands in some animals, and significantly protected animals from reactivation of virus during immunosuppression 2 months after infection. The combination of ACV + IF offered no increased antiviral activity compared to ACV alone and failed to protect animals from reactivation. In these experiments the overall antiviral activity of ACV alone was greater than IF and the combination of ACV + IF.

摘要

采用气管内接种正常小鼠建立致死性巨细胞病毒性肺炎的小鼠模型,以研究单独及联合使用阿昔洛韦(ACV)和干扰素(IF)进行抗病毒治疗的效果。感染前一天腹腔注射500单位成纤维细胞IF,感染后3小时内开始腹腔注射100mg/kg/天ACV,连续7天,二者在预防死亡方面均非常有效。与未治疗动物的情况相比,每种药物在感染后7天均降低了治疗动物肺匀浆中的病毒滴度。然而,与IF不同,ACV在14天时减少了肺内病毒生长,在一些动物中防止了病毒扩散至脾脏和唾液腺,并在感染后2个月免疫抑制期间显著保护动物免受病毒再激活。与单独使用ACV相比,ACV + IF联合用药未显示出增强的抗病毒活性,且未能保护动物免受病毒再激活。在这些实验中,单独使用ACV的总体抗病毒活性大于IF以及ACV + IF联合用药。

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