Division of Viral Products, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USA.
Division of Viral Products, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD 20993, USA.
Vaccine. 2023 Jun 29;41(29):4302-4312. doi: 10.1016/j.vaccine.2023.05.068. Epub 2023 Jun 8.
Most seasonal influenza vaccines are produced using hemagglutinin (HA) surface antigens from inactivated virions. However, virions are thought to be a suboptimal source for the less abundant neuraminidase (NA) surface antigen, which is also protective against severe disease. Here, we demonstrate that inactivated influenza virions are compatible with two modern approaches for improving protective antibody responses against NA. Using a DBA/2J mouse model, we show that the strong infection-induced NA inhibitory (NAI) antibody responses are only achieved by high dose immunizations of inactivated virions, likely due to the low viral NA content. Based on this observation, we first produced virions with higher NA content by using reverse genetics to exchange the viral internal gene segments. Single immunizations with these inactivated virions showed enhanced NAI antibody responses and improved NA-based protection from a lethal viral challenge while also allowing for the development of natural immunity to the heterotypic challenge virus HA. Second, we combined inactivated virions with recombinant NA protein antigens. These combination vaccines increased NA-based protection following viral challenge and elicited stronger antibody responses against NA than either component alone, especially when the NAs possessed similar antigenicity. Together, these results indicate that inactivated virions are a flexible platform that can be easily combined with protein-based vaccines to improve protective antibody responses against influenza antigens.
大多数季节性流感疫苗是使用来自灭活病毒粒子的血凝素 (HA) 表面抗原生产的。然而,病毒粒子被认为是神经氨酸酶 (NA) 表面抗原的不太理想的来源,神经氨酸酶也是对抗严重疾病的保护因子。在这里,我们证明了灭活流感病毒粒子与两种提高针对 NA 的保护性抗体反应的现代方法兼容。使用 DBA/2J 小鼠模型,我们表明,只有通过高剂量免疫灭活病毒粒子才能实现强烈的感染诱导的 NA 抑制 (NAI) 抗体反应,这可能是由于病毒 NA 含量低所致。基于这一观察结果,我们首先通过使用反向遗传学来交换病毒的内部基因片段来生产具有更高 NA 含量的病毒粒子。这些灭活病毒粒子的单次免疫接种显示出增强的 NAI 抗体反应和改善的基于 NA 的保护作用,可抵抗致命病毒挑战,同时也允许对异型挑战病毒 HA 产生自然免疫力。其次,我们将灭活病毒粒子与重组 NA 蛋白抗原结合。这些组合疫苗在病毒挑战后增加了基于 NA 的保护作用,并引起了针对 NA 的更强抗体反应,比单独使用任何一种成分都要强,尤其是当 NAs 具有相似的抗原性时。总之,这些结果表明,灭活病毒粒子是一种灵活的平台,可以与基于蛋白的疫苗轻松结合,以提高针对流感抗原的保护性抗体反应。