Department of Virology, Institute of Experimental Medicine, 12, acad. Pavlova street, Saint Petersburg, Russia.
WHO Collaborating Centre for Reference and Research on Influenza, Victorian Infectious Diseases Reference Laboratory at The Peter Doherty Institute for Infection & Immunity, Melbourne, Australia.
Infect Genet Evol. 2018 Oct;64:95-104. doi: 10.1016/j.meegid.2018.06.019. Epub 2018 Jun 19.
Live attenuated influenza vaccines (LAIVs) are promising tools for the induction of broad protection from influenza due to their ability to stimulate cross-reactive T cells against influenza pathogens. One of the major targets for cytotoxic T-cell immunity is viral nucleoprotein (NP), which is relatively conserved among antigenically distant influenza viruses. Nevertheless, a diversity of epitope composition has been found in the NP protein of different lineages of influenza A viruses. The H2N2 master donor virus which is currently used as a backbone for the LAIV and donor of the six genomic segments encoding the internal proteins, A/Leningrad/134/17/57 (MDV Len/17), was isolated 60 years ago. As such, NP-specific T-cell immunity induced upon vaccination with classical LAIVs with a 6:2 genome composition containing this older NP might be suboptimal against currently circulating influenza viruses. In this study, a panel of H3N2 LAIV candidates with wild-type NP genes derived from circulating viruses were generated by reverse genetics (5:3 genome composition). These viruses displayed the cold adaptation and temperature sensitivity phenotypes of MDV Len/17 in vitro. LAIVs with both 6:2 and 5:3 genome compositions were attenuated and replicated to a similar extent in the upper respiratory tract of ferrets. LAIVs were immunogenic as high neutralizing and hemagglutination inhibition serum antibody titers were detected 21 days after infection. All vaccinated animals were protected against infection with heterologous H3N2 influenza A viruses. Thus, LAIV with a 5:3 genome composition is safe, immunogenic and can induce cross-protective immunity.
减毒活流感疫苗(LAIVs)因其能够刺激针对流感病原体的交叉反应性 T 细胞而成为诱导广泛流感保护的有前途的工具。细胞毒性 T 细胞免疫的主要靶标之一是病毒核蛋白(NP),它在抗原上与不同的流感病毒相对保守。然而,在不同流感 A 病毒谱系的 NP 蛋白中发现了多种表位组成。目前用作 LAIV 骨架和编码内部蛋白的六个基因组片段供体的 H2N2 主供体病毒(A/Leningrad/134/17/57 [MDV Len/17])于 60 年前分离。因此,用包含这种较旧 NP 的经典 LAIV 进行疫苗接种所诱导的针对 NP 的 T 细胞免疫可能针对目前流行的流感病毒不太理想。在这项研究中,通过反向遗传学(5:3 基因组组成)生成了一组源自循环病毒的具有野生型 NP 基因的 H3N2 LAIV 候选物。这些病毒在体外表现出 MDV Len/17 的冷适应和温度敏感性表型。具有 6:2 和 5:3 基因组组成的 LAIV 均被减弱,在上呼吸道中以相似的程度复制。LAIV 具有免疫原性,因为在感染后 21 天检测到高中和血凝抑制血清抗体滴度。所有接种疫苗的动物均免受异源 H3N2 流感 A 病毒的感染。因此,具有 5:3 基因组组成的 LAIV 是安全的、免疫原性的并且可以诱导交叉保护免疫。