González-Domínguez Irene, Martínez Jose Luis, Slamanig Stefan, Lemus Nicholas, Liu Yonghong, Lai Tsoi Ying, Carreño Juan Manuel, Singh A Gagandeep, Singh B Gagandeep, Schotsaert Michael, Mena Ignacio, McCroskery Stephen, Coughlan Lynda, Krammer Florian, García-Sastre Adolfo, Palese Peter, Sun Weina
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Global Health Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
bioRxiv. 2022 Mar 22:2022.03.21.485247. doi: 10.1101/2022.03.21.485247.
Equitable access to vaccines is necessary to limit the global impact of the coronavirus disease 2019 (COVID-19) pandemic and the emergence of new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants. In previous studies, we described the development of a low-cost vaccine based on a Newcastle Disease virus (NDV) expressing the prefusion stabilized spike protein from SARS-CoV-2, named NDV-HXP-S. Here, we present the development of next-generation NDV-HXP-S variant vaccines, which express the stabilized spike protein of the Beta, Gamma and Delta variants of concerns (VOC). Combinations of variant vaccines in bivalent, trivalent and tetravalent formulations were tested for immunogenicity and protection in mice. We show that the trivalent preparation, composed of the ancestral Wuhan, Beta and Delta vaccines, substantially increases the levels of protection and of cross-neutralizing antibodies against mismatched, phylogenetically distant variants, including the currently circulating Omicron variant.
公平获取疫苗对于限制2019冠状病毒病(COVID-19)大流行的全球影响以及新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的出现至关重要。在先前的研究中,我们描述了一种基于表达来自SARS-CoV-2的预融合稳定刺突蛋白的新城疫病毒(NDV)的低成本疫苗的开发,名为NDV-HXP-S。在此,我们展示了下一代NDV-HXP-S变体疫苗的开发,该疫苗表达了关注的β、γ和δ变体(VOC)的稳定刺突蛋白。测试了二价、三价和四价配方的变体疫苗组合在小鼠中的免疫原性和保护作用。我们表明,由原始武汉、β和δ疫苗组成的三价制剂显著提高了针对不匹配的、系统发育距离较远的变体(包括当前流行的奥密克戎变体)的保护水平和交叉中和抗体水平。