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首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >Intranasal Immunization of Mice with Inactivated Virus and Mast Cell Activator C48/80 Elicits Protective Immunity against Influenza H1 but not H5
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Intranasal Immunization of Mice with Inactivated Virus and Mast Cell Activator C48/80 Elicits Protective Immunity against Influenza H1 but not H5

机译:用灭活病毒和肥大细胞激活剂C48 / 80对小鼠进行鼻内免疫可产生针对H1流感而非H5的保护性免疫

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摘要

Vaccination represents the most economic and effective strategy of preventing influenza pandemics. We previously demonstrated that intranasal immunization of mice with recombinant hemagglutinin and the mast cell activator C48/80 elicited protective immunity against challenge with the 2009 pandemic H1N1 influenza in mice, demonstrating that the novel C48/80 mucosal adjuvant was safe and effective. The present study demonstrated that intranasal immunization with inactivated H1N1 virus and C48/80 elicited protective immunity against lethal challenge with homologous virus, however, when the immunogen was replaced with inactivated H5N1 virus protection was lost. These observations suggested that the adjuvant effects conferred by C48/80 were virus subtype specific and that its use as a broad-spectrum adjuvant for use in immunizations against all influenza viruses needs to be further analyzed.
机译:接种疫苗是预防流感大流行的最经济,最有效的策略。我们以前证明重组鼻血凝素和肥大细胞激活剂C48 / 80对小鼠进行鼻内免疫可引起针对小鼠2009年大流行H1N1流感的攻击性保护性免疫,证明新型C48 / 80粘膜佐剂是安全有效的。本研究表明,用灭活的H1N1病毒和C48 / 80进行鼻内免疫可引起针对同源病毒致死性攻击的保护性免疫,但是当用灭活的H5N1病毒替代免疫原时,其保护作用就消失了。这些观察结果表明,C48 / 80赋予的佐剂作用是病毒亚型特异性的,需要进一步分析其作为广谱佐剂用于针对所有流感病毒的免疫接种。

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