首页> 美国卫生研究院文献>Virology Journal >An H5N1 M2e-based multiple antigenic peptide vaccine confers heterosubtypic protection from lethal infection with pandemic 2009 H1N1 virus
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An H5N1 M2e-based multiple antigenic peptide vaccine confers heterosubtypic protection from lethal infection with pandemic 2009 H1N1 virus

机译:基于H5N1 M2e的多抗原肽疫苗可赋予异亚型保护使其免受2009 H1N1大流行性病毒的致命感染

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摘要

BackgroundA 2009 global influenza pandemic caused by a novel swine-origin H1N1 influenza A virus has posted an increasing threat of a potential pandemic by the highly pathogenic avian influenza (HPAI) H5N1 virus, driving us to develop an influenza vaccine which confers cross-protection against both H5N1 and H1N1 viruses. Previously, we have shown that a tetra-branched multiple antigenic peptide (MAP) vaccine based on the extracellular domain of M2 protein (M2e) from H5N1 virus (H5N1-M2e-MAP) induced strong immune responses and cross-protection against different clades of HPAI H5N1 viruses. In this report, we investigated whether such M2e-MAP presenting the H5N1-M2e consensus sequence can afford heterosubtypic protection from lethal challenge with the pandemic 2009 H1N1 virus.
机译:背景技术由新型猪源性H1N1甲型流感病毒引起的2009年全球流感大流行已报告了高致病性禽流感(HPAI)H5N1病毒对潜在大流行的威胁不断增加,驱使我们开发出可以交叉防御的流感疫苗H5N1和H1N1病毒。以前,我们已经表明,基于H5N1病毒(H5N1-M2e-MAP)的M2蛋白(M2e)的细胞外结构域的四支多抗原肽(MAP)疫苗诱导了强大的免疫反应和针对不同进化枝的交叉保护HPAI H5N1病毒。在本报告中,我们调查了呈现H5N1-M2e共有序列的M2e-MAP是否能够提供2009年大流行H1N1病毒致死性攻击的异亚型保护。

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