Oshansky Christine M, King James, Lu Di, Zhou James, Pavetto Corrina, Horwith Gary, Biscardi Karen, Nguyen Bai, Treanor John J, Chen Li-Mei, Jepson Brett, Bright Rick A, Johnson Robert A, Cioce Vittoria, Donis Ruben O
Biomedical Advanced Research and Development Authority (BARDA), Office of the Assistant Secretary for Preparedness and Response (ASPR), Department of Health and Human Services (HHS), Washington, DC, USA.
Rho, Inc., Durham, NC, USA.
NPJ Vaccines. 2021 Mar 19;6(1):41. doi: 10.1038/s41541-021-00287-7.
An unprecedented number of human infections with avian influenza A(H7N9) in the fifth epidemic wave during the winter of 2016-2017 in China and their antigenic divergence from the viruses that emerged in 2013 prompted development of updated vaccines for pandemic preparedness. We report on the findings of a clinical study in healthy adults designed to evaluate the safety and immunogenicity of three dose levels of recombinant influenza vaccine derived from highly pathogenic A/Guangdong/17SF003/2016 (H7N9) virus adjuvanted with AS03 or MF59 oil-in water emulsions. Most of the six study groups meet the FDA CBER-specified vaccine licensure criterion of 70% seroprotection rate (SPR) for hemagglutination inhibition antibodies to the homologous virus. A substantial proportion of subjects show high cross-reactivity to antigenically distinct heterologous A(H7N9) viruses from the first epidemic wave of 2013. These results provide critical information to develop a pandemic response strategy and support regulatory requirements for vaccination under Emergency Use Authorization.
2016 - 2017年冬季中国第五波疫情期间,甲型H7N9禽流感病毒感染人类的病例数量空前,且该病毒与2013年出现的病毒存在抗原差异,这促使人们开发更新的大流行防范疫苗。我们报告了一项针对健康成年人的临床研究结果,该研究旨在评估三种剂量水平的重组流感疫苗的安全性和免疫原性,这些疫苗由高致病性A/广东/17SF003/2016(H7N9)病毒制备,并佐以AS03或MF59水包油乳剂。六个研究组中的大多数都达到了美国食品药品监督管理局生物制品评估和研究中心(FDA CBER)规定的疫苗许可标准,即针对同源病毒的血凝抑制抗体血清保护率(SPR)达到70%。相当一部分受试者对2013年第一波疫情中抗原性不同的异源A(H7N9)病毒表现出高交叉反应性。这些结果为制定大流行应对策略提供了关键信息,并支持紧急使用授权下疫苗接种的监管要求。