A Newcastle disease virus expressing a stabilized spike protein of SARS-CoV-2 induces protective immune responses

Weina Sun(Icahn School of Medicine at Mount Sinai), Yonghong Liu(Icahn School of Medicine at Mount Sinai), Fatima Amanat(Icahn School of Medicine at Mount Sinai), Irene González‐Domínguez(Icahn School of Medicine at Mount Sinai), Stephen McCroskery(Icahn School of Medicine at Mount Sinai), Stefan Slamanig(Icahn School of Medicine at Mount Sinai), Lynda Coughlan(University of Maryland, Baltimore), Victoria Rosado(Icahn School of Medicine at Mount Sinai), Nicholas Lemus(Icahn School of Medicine at Mount Sinai), Sonia Jangra(Icahn School of Medicine at Mount Sinai), Raveen Rathnasinghe(Icahn School of Medicine at Mount Sinai), Michael Schotsaert(Icahn School of Medicine at Mount Sinai), José Luis Martínez(Icahn School of Medicine at Mount Sinai), Kaori Sano(Icahn School of Medicine at Mount Sinai), Ignacio Mena(Icahn School of Medicine at Mount Sinai), Bruce L. Innis(Program for Appropriate Technology in Health), Ponthip Wirachwong(Government of Thailand), Duong Huu Thai(Institute of Vaccine and Medical Biologicals), Ricardo das Neves Oliveira(Instituto Butantan), Rami Scharf(Program for Appropriate Technology in Health), Richard Hjorth(Program for Appropriate Technology in Health), Rama Raghunandan(Program for Appropriate Technology in Health), Florian Krammer(Icahn School of Medicine at Mount Sinai), Adolfo García‐Sastre(Icahn School of Medicine at Mount Sinai), Peter Palese(Icahn School of Medicine at Mount Sinai)
Nature Communications
October 27, 2021
Cited by 120Open Access
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Abstract

Rapid development of COVID-19 vaccines has helped mitigating SARS-CoV-2 spread, but more equitable allocation of vaccines is 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 candidate based on Newcastle disease virus (NDV) that can be manufactured at high yields in embryonated eggs. Here, we show that the NDV vector expressing an optimized spike antigen (NDV-HXP-S) is a versatile vaccine inducing protective antibody responses. NDV-HXP-S can be administered intramuscularly as inactivated vaccine or intranasally as live vaccine. We show that NDV-HXP-S GMP-produced in Vietnam, Thailand and Brazil is effective in the hamster model. Furthermore, we show that intramuscular vaccination with NDV-HXP-S reduces replication of tested variants of concerns in mice. The immunity conferred by NDV-HXP-S effectively counteracts SARS-CoV-2 infection in mice and hamsters.


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