The long-term immunogenicity of an inactivated split-virion 2009 pandemic influenza A H1N1 vaccine: Randomized, observer-masked, single-center clinical study

Results in immunology Pub Date : 2012-01-01 Epub Date: 2012-10-09 DOI:10.1016/j.rinim.2012.10.001
Zhongdong Yang , Shilei Wang , Wei Li , Changgui Li , Jinrong Dong , Fangjun Li , Shuqiao Wang , Wenqing Chai , Bing Sun , Ze Chen
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引用次数: 4

Abstract

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.

一种灭活分裂病毒体2009大流行性甲型H1N1流感疫苗的长期免疫原性:随机、观察者屏蔽、单中心临床研究
本研究旨在探讨2009年甲型H1N1大流行性流感病毒颗粒灭活疫苗单次免疫后的长期免疫原性。我们招募了480名年龄在18-60岁之间的成年人,进行安慰剂对照、观察者屏蔽、单中心临床研究。我们将受试者随机分为四组:15 μg、30 μg和45 μg血凝素(HA)剂量组和安慰剂对照组。最终,259名受试者完成了整个研究。所有三个剂量组的血清转换率和血清保护率以及几何平均增加(GMI)在接种后180天内均符合欧洲药品管理局(EMEA)对流感疫苗的标准。然而,在接种后360天,所有剂量组的血清保护率均低于70%,而血清转化率和GMI在此时间点继续满足许可标准。综上所述,单剂量15 μg的HA疫苗可在成人中诱导持续至少6个月的保护性免疫反应。这项研究可能有助于未来开发具有长期免疫功能的流感疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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