Xia Ming, Huang Pengwei, Vago Frank S, Jiang Wen, Tan Ming
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department of Biological Sciences, Purdue University, West Lafayette, IN, USA.
Vaccine. 2025 Feb 6;46:126585. doi: 10.1016/j.vaccine.2024.126585. Epub 2024 Dec 7.
The continually high disease burden of influenza and the relatively low effectiveness of current influenza vaccines call for enhanced vaccine strategies. We previously generated unique S-HA1 pseudovirus nanoparticles (PVNPs) displaying the receptor binding HA1 antigens of the H7N9 subtype as an influenza vaccine candidate and characterized their features in biochemistry, biophysics, structure, and immune response. In this follow up study, we created new S-HA1 PVNPs displaying the HA1 antigens of other common influenza viruses, including two H1N1 strains, one H3N2 strain, and an influenza B virus, respectively. The recombinant PVNPs react well with antibodies against hemagglutinins (HAs) or mouse sera obtained after influenza virus challenge. 3D structural models were constructed to comprehend the structural features and size variations of the S-HA1 PVNPs. The PVNPs are immunogenic, eliciting high titers of HA1-specific serum antibodies that recognized commercial HA1 proteins. Importantly, the S-HA1 PVNP representing the H1N1 PR8 strain provided mice with 100 % protection against mortality caused by challenge with the mouse-adapted influenza virus of the same PR8 strain. The S-HA1 PVNP representing the H1N1 2009 pandemic strain conferred mice with 50 % protection against mortality caused by challenge with the 1934 PR8 strain, despite the two strains circulating 75 years apart. Our data demonstrated the feasibility of generating S-HA1 PVNPs to display HA1 antigens of diverse influenza A and B viruses. The readily available S-HA1 PVNPs hold promise as influenza vaccines, presenting a novel approach to combat the deadly influenza disease.
流感持续的高疾病负担以及当前流感疫苗相对较低的有效性,都需要加强疫苗策略。我们之前制备了独特的S-HA1假病毒纳米颗粒(PVNPs),其展示了H7N9亚型的受体结合HA1抗原,作为一种流感疫苗候选物,并在生物化学、生物物理学、结构和免疫反应方面对其特征进行了表征。在这项后续研究中,我们分别制备了展示其他常见流感病毒HA1抗原的新型S-HA1 PVNPs,包括两种H1N1毒株、一种H3N2毒株和一种B型流感病毒。重组PVNPs与抗血凝素(HAs)抗体或流感病毒攻击后获得的小鼠血清反应良好。构建了三维结构模型以了解S-HA1 PVNPs的结构特征和大小变化。PVNPs具有免疫原性,可诱导产生高滴度的识别商业HA1蛋白的HA1特异性血清抗体。重要的是,代表H1N1 PR8毒株的S-HA1 PVNP为小鼠提供了100%的保护,使其免受相同PR8毒株的小鼠适应流感病毒攻击所致的死亡。代表2009年H1N1大流行毒株的S-HA1 PVNP使小鼠对1934年PR8毒株攻击所致的死亡有50%的保护作用,尽管这两种毒株相隔75年流行。我们的数据证明了制备S-HA1 PVNPs以展示多种甲型和乙型流感病毒HA1抗原的可行性。易于获得的S-HA1 PVNPs有望成为流感疫苗,为对抗致命的流感疾病提供了一种新方法。