首页> 美国卫生研究院文献>Results in Immunology >The long-term immunogenicity of an inactivated split-virion 2009 pandemic influenza A H1N1 vaccine: Randomized observer-masked single-center clinical study
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The long-term immunogenicity of an inactivated split-virion 2009 pandemic influenza A H1N1 vaccine: Randomized observer-masked single-center clinical study

机译:灭活的分裂病毒2009大流行性甲型H1N1流感疫苗的长期免疫原性:随机观察者遮盖的单中心临床研究

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摘要

The aim of this study is to investigate the long-term immunogenicity of inactivated split-virion 2009 pandemic influenza A H1N1 vaccine after a single immunization. We recruited 480 adults, aged 18–60 years, for a placebo-controlled, observer-masked, single-center clinical study. We randomly assigned subjects into four groups: 15 μg, 30 μg and 45 μg of hemagglutinin (HA) dosage groups, and a placebo control group. Finally, 259 subjects completed the entire study. The rates of seroconversion and seroprotection and the geometric mean increase (GMI) fulfilled the criteria of the European Medicines Agency (EMEA) for influenza vaccine for 180 days after vaccination in all three dosage groups. However, the seroprotection rates of all dosage groups were below 70% at day 360 post vaccination, while the seroconversion rates and the GMI continued to meet the licensure criteria at this time point. In conclusion, a single dose of 15 μg HA vaccine could induce a protective immune response persisting for at least six months in adults. This study could be beneficial for the future development of influenza vaccines conferring long-term immunity.
机译:这项研究的目的是调查单次免疫后灭活的2009年分裂病毒大流行性甲型H1N1流感疫苗的长期免疫原性。我们招募了480位18至60岁的成年人,进行安慰剂对照,观察者掩盖的单中心临床研究。我们将受试者随机分为四组:15μg,30μg和45μμg血凝素(HA)剂量组和安慰剂对照组。最后,有259名受试者完成了整个研究。在所有三个剂量组中接种疫苗180天后,血清转化和血清保护的速率以及几何平均数增加(GMI)达到了欧洲药品管理局(EMEA)的流感疫苗标准。但是,在接种后第360天,所有剂量组的血清保护率均低于70%,而此时血清转化率和GMI仍符合许可标准。总之,单剂15μgHA疫苗可诱导保护性免疫应答在成人中持续至少六个月。这项研究可能有益于赋予长期免疫力的流感疫苗的未来发展。

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