Sun Xiangjie, Belser Jessica A, Pulit-Penaloza Joanna A, Creager Hannah M, Guo Zhu, Jefferson Stacie N, Liu Feng, York Ian A, Stevens James, Maines Taronna R, Jernigan Daniel B, Katz Jacqueline M, Levine Min Z, Tumpey Terrence M
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States; Emory University, Atlanta, GA 30322, United States.
Virology. 2017 Aug;508:164-169. doi: 10.1016/j.virol.2017.05.010. Epub 2017 May 26.
Avian influenza viruses, notably H5 subtype viruses, pose a continuous threat to public health due to their pandemic potential. In recent years, influenza virus H5 subtype split vaccines with novel oil-in-water emulsion based adjuvants (e.g. AS03, MF59) have been shown to be safe, immunogenic, and able to induce broad immune responses in clinical trials, providing strong scientific support for vaccine stockpiling. However, whether such vaccines can provide protection from infection with emerging, antigenically distinct clades of H5 viruses has not been adequately addressed. Here, we selected two AS03-adjuvanted H5N1 vaccines from the US national pre-pandemic influenza vaccine stockpile and assessed whether the 2004-05 vaccines could provide protection against a 2014 highly pathogenic avian influenza (HPAI) H5N2 virus (A/northern pintail/Washington/40964/2014), a clade 2.3.4.4 virus responsible for mass culling of poultry in North America. Ferrets received two doses of adjuvanted vaccine containing 7.5µg of hemagglutinin (HA) from A/Vietnam/1203/2004 (clade 1) or A/Anhui/1/2005 (clade 2.3.4) virus either in a homologous or heterologous prime-boost vaccination regime. We found that both vaccination regimens elicited robust antibody responses against the 2004-05 vaccine viruses and could reduce virus-induced morbidity and viral replication in the lower respiratory tract upon heterologous challenge despite the low level of cross-reactive antibody titers to the challenge H5N2 virus. This study supports the value of existing stockpiled 2004-05 influenza H5N1 vaccines, combined with AS03-adjuvant for early use in the event of an emerging pandemic with H5N2-like clade 2.3.4.4 viruses.
禽流感病毒,尤其是H5亚型病毒,因其具有大流行的潜力,对公众健康构成持续威胁。近年来,基于新型水包油乳剂佐剂(如AS03、MF59)的H5亚型流感病毒裂解疫苗在临床试验中已显示出安全、具有免疫原性,并且能够诱导广泛的免疫反应,为疫苗储备提供了有力的科学支持。然而,此类疫苗能否对新出现的、抗原性不同的H5病毒分支感染提供保护,尚未得到充分研究。在此,我们从美国国家大流行前流感疫苗储备中选取了两种AS03佐剂的H5N1疫苗,并评估2004 - 2005年的疫苗是否能抵御2014年高致病性禽流感(HPAI)H5N2病毒(A/针尾鸭/华盛顿/40964/2014),这是一种2.3.4.4分支病毒,曾导致北美大量家禽被扑杀。雪貂接受两剂含有7.5μg来自A/越南/1203/2004(分支1)或A/安徽/1/2005(分支2.3.4)病毒血凝素(HA)的佐剂疫苗,采用同源或异源初免 - 加强免疫方案。我们发现,尽管对攻击的H5N2病毒的交叉反应抗体滴度较低,但两种免疫方案均能引发针对2004 - 2005年疫苗病毒的强劲抗体反应,并且在异源攻击后能够降低病毒诱导的发病率以及下呼吸道中的病毒复制。本研究支持现有储备的2004 - 2005年H5N1流感疫苗与AS03佐剂相结合在出现类似2.3.4.4分支H5N2病毒的大流行时早期使用的价值。