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首页> 外文期刊>Virology >Vaccination with recombinant adenoviruses expressing Ebola virus glycoprotein elicits protection in the interferon alpha/beta receptor knock-out mouse
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Vaccination with recombinant adenoviruses expressing Ebola virus glycoprotein elicits protection in the interferon alpha/beta receptor knock-out mouse

机译:表达埃博拉病毒糖蛋白的重组腺病毒疫苗在干扰素α/β受体敲除小鼠中引起保护

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摘要

The resistance of adult immunocompetent mice to infection with ebolaviruses has led to the development of alternative small animal models that utilise immunodeflcient mice, for example the interferon alpha/beta receptor knock-out mouse (IFNR~(-/-)). IFNR~(-/-) mice have been shown to be susceptible to infection with ebolaviruses by multiple routes but it is not known if this murine model is suitable for testing therapeutics that rely on the generation of an immune response for efficacy. We have tested recombinant adenovirus vectors for their ability to protect IFNR~(-/-) mice from challenge with Ebola virus and have analysed the humoral response generated after immunisation. The recombinant vaccines elicited good levels of protection in the knock-out mouse and the antibody response in IFNR~(-/-) mice was similar to that observed in vaccinated wild-type mice. These results indicate that the IFNR~(-/-) mouse is a relevant small animal model for studying ebolavirus-specific therapeutics.
机译:成年免疫能力强的小鼠对埃博拉病毒感染的抗性导致开发了利用免疫缺陷型小鼠的其他小型动物模型,例如干扰素α/β受体敲除小鼠(IFNR-(-/-))。 IFNR(-/-)小鼠已显示易受埃博拉病毒感染的多种途径感染,但尚不知道这种小鼠模型是否适合测试依赖免疫应答产生功效的治疗剂。我们测试了重组腺病毒载体保护IFNR〜(-/-)小鼠免受埃博拉病毒攻击的能力,并分析了免疫后产生的体液反应。重组疫苗在敲除小鼠中引起了良好的保护水平,并且在IFNR-(-/-)小鼠中的抗体反应与在接种的野生型小鼠中观察到的相似。这些结果表明,IFNR-(-/-)小鼠是用于研究埃博拉病毒特异性疗法的相关小动物模型。

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