| Literature DB >> 33348607 |
Weina Sun1, Stephen McCroskery1, Wen-Chun Liu1,2,3, Sarah R Leist4, Yonghong Liu1, Randy A Albrecht1,2, Stefan Slamanig1, Justine Oliva1, Fatima Amanat1,5, Alexandra Schäfer4, Kenneth H Dinnon6, Bruce L Innis7, Adolfo García-Sastre1,2,8,9, Florian Krammer1, Ralph S Baric4,6, Peter Palese1,8.
Abstract
A successful severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine must not only be safe and protective, but must also meet the demand on a global scale at a low cost. Using the current influenza virus vaccine production capacity to manufacture an egg-based inactivated Newcastle disease virus (NDV)/SARS-CoV-2 vaccine would meet that challenge. Here, we report pre-clinical evaluations of an inactivated NDV chimera stably expressing the membrane-anchored form of the spike (NDV-S) as a potent coronavirus disease 2019 (COVID-19) vaccine in mice and hamsters. The inactivated NDV-S vaccine was immunogenic, inducing strong binding and/or neutralizing antibodies in both animal models. More importantly, the inactivated NDV-S vaccine protected animals from SARS-CoV-2 infections. In the presence of an adjuvant, antigen-sparing could be achieved, which would further reduce the cost while maintaining the protective efficacy of the vaccine.Entities:
Keywords: COVID-19; adjuvant; antigen-sparing; egg-based vaccine; hamster model; mouse-adapted SARS-CoV-2
Year: 2020 PMID: 33348607 PMCID: PMC7766959 DOI: 10.3390/vaccines8040771
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X