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一种MF59佐剂H5N1大流行前流感疫苗在接种同源或异源H5N1疫苗的健康成年人中的安全性和免疫原性:一项观察性研究。

The safety and immunogenicity of a MF59-adjuvanted H5N1 prepandemic influenza vaccine in healthy adults primed with homologous or heterologous H5N1 vaccines: an observational study.

作者信息

Wei Sung-Hsi, Liu Ming-Tsan, Tsai Yao-Chou, Liao Chung-Hsin, Chen Chih-Ming, Wang Wei-Yao, Huang Yi-Lung, Chang Feng-Yee, Chou Pesus

机构信息

Community Medicine Research Center and Institute of Public Health, National Yang-Ming University, No 155, Sec 2, Linong St., Beitou Dist, Taipei City, 112, Taiwan.

Centers for Disease Control, No.6, Linsen S Rd, Zhongzheng Dist, Taipei City, 10050, Taiwan.

出版信息

BMC Infect Dis. 2014 Nov 14;14:587. doi: 10.1186/s12879-014-0587-z.

Abstract

BACKGROUND

World Health Organization (WHO) has recommended individuals with increased risk of contracting influenza A H5N1 infection to be immunized against the virus during the inter-pandemic period. Safety and immunogenicity of H5N1 vaccine among participants primed with homologous or heterologous H5N1 vaccines produced by diverse manufactures have not been reported.

METHODS

Healthy individuals aged 20 to 60 years old were recruited and stratified into three groups: participants without priming (control group), participants primed with A/Indonesia/05/2005 vaccine, participants primed with A/Vietnam/1194/2004 vaccine and A/Indonesia/05/2005 vaccine. Enrolled participants received two doses of MF59-adjuvanted A/Vietnam/1194/2004 vaccine (study vaccine). Solicited reactions were recorded by vaccine recipients. Blood samples were obtained for hemagglutination inhibition test.

RESULTS

A total of 131 participants were enrolled. No significant adverse events were recorded. Tenderness, fatigue and general muscle ache were the most common solicited reactions which alleviated within one week of immunization. Three weeks after two doses of the study vaccine, 63%, 68% and 88% were in seroprotective status in the control group, A/Indonesia/05/2005 primed group and A/Vietnam/1194/2004 and A/Indonesia/05/2005 primed group, respectively. Participants primed with A/Vietnam/1194/2004 and A/Indonesia/05/2005 showed high immune response after booster with one dose of the study vaccine.

CONCLUSION

The study vaccine did not cause severe adverse events. It elicited mostly mild to moderate reactions among participants. Participants primed with A/Vietnam/1194/2004 and A/Indonesia/05/2005 vaccine showed higher immune response than those without priming or primed with A/Indonesia/05/2005 vaccine. The report suggested those with an increased risk of influenza A H5N1 virus exposure may benefit from receiving influenza A H5N1 priming during the inter-pandemic period if the antigenicity of the pandemic influenza strain is similar to that of the priming strain.

摘要

背景

世界卫生组织(WHO)建议,在大流行间期,感染甲型H5N1流感风险增加的个体应接种该病毒疫苗。不同厂家生产的同源或异源H5N1疫苗在接种者中的安全性和免疫原性尚未见报道。

方法

招募20至60岁的健康个体,并将其分为三组:未接种疫苗的参与者(对照组)、接种A/印度尼西亚/05/2005疫苗的参与者、接种A/越南/1194/2004疫苗和A/印度尼西亚/05/2005疫苗的参与者。入选的参与者接种两剂含MF59佐剂的A/越南/1194/2004疫苗(研究疫苗)。疫苗接种者记录了接种疫苗后的反应。采集血样进行血凝抑制试验。

结果

共招募了131名参与者。未记录到显著不良事件。压痛、疲劳和全身肌肉酸痛是最常见的接种疫苗后的反应,在免疫接种后一周内缓解。接种两剂研究疫苗三周后,对照组、接种A/印度尼西亚/05/2005疫苗组和接种A/越南/1194/2004疫苗及A/印度尼西亚/05/2005疫苗组的血清保护率分别为63%、68%和88%。接种A/越南/1194/2004疫苗和A/印度尼西亚/05/2005疫苗的参与者在接种一剂研究疫苗加强免疫后显示出高免疫反应。

结论

研究疫苗未引起严重不良事件。它在参与者中大多引起轻度至中度反应。接种A/越南/1194/2004疫苗和A/印度尼西亚/05/2005疫苗的参与者比未接种疫苗或接种A/印度尼西亚/05/2005疫苗的参与者显示出更高的免疫反应。该报告表明,如果大流行性流感毒株的抗原性与接种疫苗毒株相似,那么甲型H5N1病毒暴露风险增加的人群可能会从大流行间期接种甲型H5N1疫苗中受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ee7/4236496/fa791d22c815/12879_2014_Article_587_Fig1_HTML.jpg

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