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

Authors :
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 L.
Sano, Kaori
Mena, Ignacio
Innis, Bruce L.
Wirachwong, Ponthip
Thai, Duong Huu
Oliveira, Ricardo Das Neves
Scharf, Rami
Source :
Nature Communications; 10/27/2021, Vol. 12 Issue 1, p1-14, 14p
Publication Year :
2021

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. Here the authors show that a Newcastle disease virus based COVID-19 vaccine expressing a stabilized spike protein induces protective immunity in small animal models and reduces replication of variants of concerns. This vaccine candidate can be produced by influenza virus vaccine manufactures around the world. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
12
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
153241242
Full Text :
https://doi.org/10.1038/s41467-021-26499-y