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Comparison of the Long-Term Immunogenicity of Two Pandemic Influenza A/H1N1 2009 Vaccines, the MF59-Adjuvanted and Unadjuvanted Vaccines, in Adults

机译:成人两种大流行性流感A / H1N1 2009疫苗(MF59佐剂和非佐剂)的长期免疫原性比较

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Since the first reports of the A/H1N1 virus in April 2009, the pandemic influenza virus spread globally and circulated for a long time. The primary method for the control of influenza is vaccination, but levels of influenza vaccine-induced antibody are known to decline rapidly during a 6-month period. In adults aged 18 to 64 years, we compared the long-term immunogenicity of two of the influenza A/H1N1 2009 monovalent vaccines, 3.75-μg MF59-adjuvanted vaccine and 15-μg unadjuvanted vaccine. The serum hemagglutinin inhibition (HI) titers were determined prevaccination and at 1, 6, and 10 months after vaccination. One hundred six (88.3%) of the 120 subjects were monitored for the entire 10-month period after receiving the influenza A/H1N1 2009 monovalent vaccine. There were 60 patients who received the unadjuvanted vaccine and 46 patients who received the MF59-adjuvanted vaccine. The seroprotection rates, seroconversion rates, and the geometric mean titer (GMT) folds fulfilled the criteria of the European Medicines Agency (EMA) for influenza A/California/7/2009 (H1N1) at 1 month after vaccination irrespective of the vaccine composition. Although the GMTs at 1 month postvaccination were somewhat higher in the unadjuvanted vaccine recipients than in the MF59-adjuvanted vaccine recipients, the difference was not significant (P = 0.29). The seroprotection rates at 6 and 10 months postvaccination were preserved above 70% but only in the MF59-adjuvanted vaccine recipients. In conclusion, low-dose MF59-adjuvanted influenza vaccine, even with 3.75 μg hemagglutinin antigen, might induce excellent long-term immunity that is comparable to the conventional dose of unadjuvanted vaccine among healthy adults aged 18 to 64 years.
机译:自2009年4月首次报道A / H1N1病毒以来,大流行性流感病毒在全球范围内传播并传播了很长时间。控制流感的主要方法是接种疫苗,但已知流感疫苗诱导的抗体水平在6个月内迅速下降。在18至64岁的成年人中,我们比较了两种流感A / H1N1 2009单价疫苗,3.75μgMF59佐剂疫苗和15μg非佐剂疫苗的长期免疫原性。疫苗接种前,接种后1、6和10个月测定血清血凝素抑制(HI)滴度。在接受A / H1N1 2009流感单价疫苗接种后的整个10个月期间,对120名受试者中的166名(88.3%)进行了监测。 60例患者接受了无佐剂疫苗,46例患者接受了MF59佐剂疫苗。接种疫苗后1个月的血清保护率,血清转化率和几何平均滴度(GMT)折叠均符合欧洲药品管理局(EMA)的A / California / 7/2009(H1N1)流感标准,而与疫苗成分无关。尽管未佐剂疫苗接种者在接种后1个月的GMT略高于MF59佐剂疫苗接种者,但差异并不显着( P = 0.29)。接种后6个月和10个月的血清保护率保持在70%以上,但仅在MF59佐剂的疫苗接种者中。总之,低剂量的MF59佐剂型流感疫苗,即使含有3.75μg血凝素抗原,也可以诱导出色的长期免疫性,这与18至64岁健康成人的常规剂量的非佐剂类疫苗相当。

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