在流感病毒攻击前给予小鼠Muramyl肽和多肌苷-多细胞酸可减少肺部疾病和死亡率。

P R Wyde, H R Six, M W Ambrose, B J Throop
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引用次数: 0

摘要

在小鼠流感病毒模型中检测了Muramyl二肽(MDP)、murab肽(MDP的衍生物)、小鼠α -干扰素(MoIFN)和多肌苷-多胞酸(poly (I-C))的抗流感病毒活性。在病毒攻击之前单独给药的这些化合物都不能保护小鼠免受流感病毒感染。相比之下,在甲型流感/香港/68病毒攻击前2天和在病毒攻击前1天给予MDP或murabutide的小鼠,与同样攻击的对照组小鼠相比,肺部病毒滴度和死亡率显著降低。如果用MoIFN代替poly I-C,肺部病毒滴度和死亡率没有显著降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Muramyl peptides and polyinosinic-polycytodylic acid given to mice prior to influenza virus challenge reduces pulmonary disease and mortality.

Muramyl dipeptide (MDP), murabutide (a derivative of MDP), mouse alpha-interferon (MoIFN), and polyinosinic-polycytodylic acid (poly (I-C) were tested in a mouse-influenza virus model for anti-influenza virus activity. None of these compounds administered alone prior to virus challenge had more than minimal ability to protect mice from influenza virus infection. In contrast, mice given either MDP or murabutide 2 days prior to challenge with influenza A/Hong Kong/68 virus and poly I-C 1 day prior to virus challenge had significantly reduced pulmonary virus titers and mortality compared to comparably challenged control mice. No significant reductions in pulmonary virus titers or mortality were seen if MoIFN was given in place of poly I-C in this sequence.

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