A Newcastle disease virus-vector expressing a prefusion-stabilized spike protein of SARS-CoV-2 induces protective immune responses against prototype virus and variants of concern in mice and hamsters

Sun, Weina; Liu, Yonghong; Amanat, Fatima; González-Domínguez, Irene; McCroskery, Stephen; Slamanig, Stefan; Coughlan, Lynda; Rosado, Victoria; Lemus, Nicholas; Jangra, Sonia; Rathnasinghe, Raveen; Schotsaert, Michael; Martinez, Jose; Sano, Kaori; Mena, Ignacio; Innis, Bruce L; Wirachwong, Ponthip; Thai, Duong Huu; Oliveira, Ricardo Das Neves; Scharf, Rami; Hjorth, Richard; Raghunandan, Rama; Krammer, Florian; García-Sastre, Adolfo; Palese, Peter

Rapid development of coronavirus disease 2019 (COVID-19) vaccines and expedited authorization for use and approval has been proven beneficial to mitigate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spread and given hope in this desperate situation. It is believed that sufficient supplies and equitable allocations of vaccines are necessary to limit the global impact of the COVID-19 pandemic and the emergence of additional variants of concern. We have developed a COVID-19 vaccine based on Newcastle disease virus (NDV) that can be manufactured at high yields in embryonated eggs. Here we provide evidence that the NDV vector expressing an optimized spike antigen (NDV-HXP-S), upgraded from our previous construct, is a versatile vaccine that can be used live or inactivated to induce strong antibody responses and to also cross-neutralize variants of concern. The immunity conferred by NDV-HXP-S effectively counteracts SARS-CoV-2 infection in mice and hamsters. It is noteworthy that vaccine lots produced by existing egg-based influenza virus vaccine manufacturers in Vietnam, Thailand and Brazil exhibited excellent immunogenicity and efficacy in hamsters, demonstrating that NDV-HXP-S vaccines can be quickly produced at large-scale to meet global demands.