首页> 外文期刊>Hong Kong medical journal =: Xianggang yi xue za zhi >Cross-clade immunogenicity and safety of an AS03A-adjuvanted prepandemic H5N1 influenza vaccine in Hong Kong.
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Cross-clade immunogenicity and safety of an AS03A-adjuvanted prepandemic H5N1 influenza vaccine in Hong Kong.

机译:在香港,AS03A佐剂的大流行前H5N1流感疫苗的跨疫苗免疫原性和安全性。

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OBJECTIVE: To present Hong Kong'Aispecific data from a large Asian population (also involving Thailand, Singapore, and Taiwan) on safety and manufacturing consistency across four AS03(A)-adjuvanted H5N1 vaccine formulations in terms of immune response against the A/Vietnam/1194/2004 strain. Immunogenicity against the heterologous A/Indonesia/05/2005 strain was also assessed. NCT Number: 00449670. DESIGN: Prospective, observer-blind study. SETTING: Out-patient clinic of a tertiary hospital in Hong Kong. PARTICIPANTS: A total of 360 subjects aged 18 to 60 years were randomised into six groups to receive two doses (21 days apart) of the study vaccine. INTERVENTIONS: One of the four adjuvanted formulations (3.75 microgram H5N1 haemagglutinin [HA]+AS03(A)) of the vaccine (H5N1-AS03(A)) or one of the two non-adjuvanted (3.75 microgram H5N1 [HA]) formulations of the vaccine (H5N1-DIL). MAIN OUTCOME MEASURES: Blood samples collected before vaccination and 21 days after each vaccine dose were analysed using haemagglutination-inhibition and neutralisation assays. Solicited, unsolicited, and serious adverse events were recorded. RESULTS: Manufacturing consistency across all four vaccine formulations was demonstrated. After two doses, the AS03(A)-adjuvanted prepandemic influenza vaccine demonstrated high seroprotection rates against the A/Vietnam/1194/2004 strain (95.8%) and good immunogenicity against the heterologous A/Indonesia/05/2005 strain (45.7%), as compared to the non-adjuvanted vaccine (4.6% and 1.5%, respectively). The seroconversion rates induced by the adjuvanted formulations in terms of viral neutralising antibodies against the two strains were much higher than those induced by the non-adjuvanted formulations. There were no safety concerns for any of the adjuvanted vaccine formulations. CONCLUSIONS: The AS03(A)-adjuvanted H5N1 prepandemic influenza vaccine demonstrated good immunogenicity and an acceptable safety profile in Hong Kong.
机译:目的:提供来自亚洲大批人群(也涉及泰国,新加坡和台湾)的Hong Kong'Ai特定数据,这些数据涉及四种针对AS03(A)的H5N1疫苗制剂在针对A /越南的免疫反应方面的安全性和生产一致性/ 1194/2004应变。还评估了针对异源A /印度尼西亚2005/05 /株的免疫原性。 NCT编号:00449670。设计:前瞻性,观察员盲研究。地点:香港一家三级医院的门诊。参与者:总共360名18至60岁的受试者被随机分为六组,分别接受两剂(相隔21天)的研究疫苗。干预措施:疫苗(H5N1-AS03(A))的四种佐剂制剂(3.75微克H5N1血凝素[HA] + AS03(A))之一或两种非佐剂(3.75微克H5N1 [HA])制剂之一疫苗(H5N1-DIL)。主要观察指标:使用血凝抑制和中和分析法分析疫苗接种前和每次疫苗接种后21天采集的血样。记录了主动,主动和严重不良事件。结果:证明了所有四种疫苗制剂的生产一致性。经过两剂,AS03(A)佐剂的大流行前流感疫苗对A / Vietnam / 1194/2004菌株表现出高血清保护率(95.8%),对异源A / Indonesiasia2005菌株表现出良好的免疫原性(45.7%)与非佐剂疫苗相比(分别为4.6%和1.5%)。就针对两种菌株的病毒中和抗体而言,佐剂制剂诱导的血清转化率远高于非佐剂制剂诱导的血清转化率。对于任何佐剂疫苗制剂都没有安全性问题。结论:在香港,AS03(A)佐剂的H5N1大流行前流感疫苗表现出良好的免疫原性和可接受的安全性。

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