Center for Vaccines and Immunology, University of Georgia, Athens, Georgia, USA.
Department of Infectious Diseases, University of Georgia, Athens, Georgia, USA.
J Virol. 2020 Dec 22;95(2). doi: 10.1128/JVI.01526-20.
Influenza viruses have caused numerous pandemics throughout human history. The 1957 influenza pandemic was initiated by an H2N2 influenza virus. This H2N2 influenza virus was the result of a reassortment event between a circulating H2N2 avian virus and the seasonal H1N1 viruses in humans. Previously, our group has demonstrated the effectiveness of hemagglutinin (HA) antigens derived using computationally optimized broadly reactive antigen (COBRA) methodology against H1N1, H3N2, and H5N1 viruses. Using the COBRA methodology, H2 HA COBRA antigens were designed using sequences from H2N2 viruses isolated from humans in the 1950s and 1960s, as well as H2Nx viruses isolated from avian and mammalian species between the 1950s and 2016. In this study, the effectiveness of H2 COBRA HA antigens (Z1, Z3, Z5, and Z7) was evaluated in DBA/2J mice and compared to that of wild-type H2 HA antigens. The COBRA HA vaccines elicited neutralizing antibodies to the majority of viruses in our H2 HA panel and across all three clades as measured by hemagglutination inhibition (HAI) and neutralization assays. Comparatively, several wild-type HA vaccines elicited antibodies against a majority of the viruses in the H2 HA panel. DBA/2J mice vaccinated with COBRA vaccines showed increase survival for all three viral challenges compared to the wild-type H2 vaccines. In particular, the Z1 COBRA is a promising candidate for future work toward a pandemic H2 influenza vaccine. H2N2 influenza has caused at least one pandemic in the past. Given that individuals born after 1968 have not been exposed to H2N2 influenza viruses, a future pandemic caused by H2 influenza is likely. An effective H2 influenza vaccine would need to elicit broadly cross-reactive antibodies to multiple H2 influenza viruses. Choosing a wild-type virus to create a vaccine may elicit a narrow immune response and not protect against multiple H2 influenza viruses. COBRA H2 HA vaccines were developed and evaluated in mice along with wild-type H2 HA vaccines. Multiple COBRA H2 HA vaccines protected mice from all three viral challenges and produced broadly cross-reactive neutralizing antibodies to H2 influenza viruses.
流感病毒在人类历史上引发了无数次大流行。1957 年的流感大流行是由 H2N2 流感病毒引发的。这种 H2N2 流感病毒是一种循环的 H2N2 禽流感病毒与人类季节性 H1N1 病毒重组的结果。在此之前,我们的团队已经证明了使用计算优化的广泛反应性抗原 (COBRA) 方法衍生的血凝素 (HA) 抗原对 H1N1、H3N2 和 H5N1 病毒的有效性。使用 COBRA 方法,根据我们从 20 世纪 50 年代和 60 年代从人类中分离出的 H2N2 病毒以及从 20 世纪 50 年代至 2016 年从禽类和哺乳动物物种中分离出的 H2Nx 病毒的序列设计了 H2 HA COBRA 抗原。在这项研究中,评估了 DBA/2J 小鼠中 H2 COBRA HA 抗原 (Z1、Z3、Z5 和 Z7) 的有效性,并与野生型 H2 HA 抗原进行了比较。COBRA HA 疫苗通过血凝抑制 (HAI) 和中和测定,在我们的 H2 HA 组中引起了针对大多数病毒的中和抗体,并跨越了所有三个分支。相比之下,几种野生型 HA 疫苗引起了针对 H2 HA 组中大多数病毒的抗体。与野生型 H2 疫苗相比,用 COBRA 疫苗接种的 DBA/2J 小鼠在所有三种病毒挑战中都显示出存活增加。特别是,Z1 COBRA 是未来大流行 H2 流感疫苗的有前途的候选者。H2N2 流感在过去至少引发了一次大流行。鉴于 1968 年后出生的人没有接触过 H2N2 流感病毒,未来由 H2 流感引起的大流行很可能发生。有效的 H2 流感疫苗需要针对多种 H2 流感病毒产生广泛的交叉反应性抗体。选择野生型病毒制造疫苗可能会引起狭窄的免疫反应,并且无法预防多种 H2 流感病毒。COBRA H2 HA 疫苗与野生型 H2 HA 疫苗一起在小鼠中进行了开发和评估。多种 COBRA H2 HA 疫苗可保护小鼠免受所有三种病毒的挑战,并产生针对 H2 流感病毒的广泛交叉反应性中和抗体。