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首页> 外文期刊>Cytokine >Protective effects of recombinant human granulocyte macrophage colony stimulating factor on H1N1 influenza virus-induced pneumonia in mice.
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Protective effects of recombinant human granulocyte macrophage colony stimulating factor on H1N1 influenza virus-induced pneumonia in mice.

机译:重组人粒细胞巨噬细胞集落刺激因子对H1N1流感病毒诱导的小鼠肺炎的保护作用。

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摘要

Protective effects of recombinant human granulocyte macrophage colony stimulating factor (rHuGM-CSF) on H1N1 influenza virus infection was studied in vivo and in vitro. Mice were infected with H1N1 influenza A viruses and rHuGM-CSF at doses of 0.34, 0.67, and 1.34mgkg(-1)d(-1) was administrated for 7days before the mice were infected with influenza virus and continued for a further 3days. Compared with control mice, rHuGM-CSF was demonstrated to increase the survival rate of the infected mice by 50.0%, 55.6%, and 80.0% and increased the mean survival days by 25.7%, 30.0%, and 46.8%, respectively. Histopathological study of the lungs in pneumonia mice found that pre-treatment with rHuGM-CSF significantly ameliorated lung injury induced by influenza virus infection. In vitro study demonstrated that when rHuGM-CSF were co-incubated with peripheral blood mononuclear cells (PBMCs), the PBMCs culture supernatant induced a dose-dependent reduction of virus-induced cytopathic effect (CPE) in Madin-Darby canine kidney (MDCK) cells in vitro. These results suggested that rHuGM-CSF might be an effective and potential protection for H1N1 influenza virus-induced pneumonia.
机译:体内和体外研究了重组人粒细胞巨噬细胞集落刺激因子(rHuGM-CSF)对H1N1流感病毒感染的保护作用。在小鼠感染流感病毒之前,将小鼠感染H1N1甲型流感病毒和rHuGM-CSF,剂量分别为0.34、0.67和1.34mgkg(-1)d(-1)7天,并再持续3天。与对照小鼠相比,rHuGM-CSF被证明可将感染小鼠的存活率提高50.0%,55.6%和80.0%,并将平均存活天数分别提高25.7%,30.0%和46.8%。对肺炎小鼠肺部的组织病理学研究发现,rHuGM-CSF预处理可显着减轻流感病毒感染引起的肺部损伤。体外研究表明,当将rHuGM-CSF与外周血单个核细胞(PBMC)共同孵育时,PBMCs培养上清液可导致Madin-Darby犬肾(MDCK)剂量依赖性降低病毒诱导的细胞病变作用(CPE)。体外细胞。这些结果表明,rHuGM-CSF可能是对H1N1流感病毒引起的肺炎的有效和潜在的保护。

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