| Literature DB >> 35350201 |
Irene González-Domínguez1, Jose Luis Martínez1, Stefan Slamanig1, Nicholas Lemus1, Yonghong Liu1, Tsoi Ying Lai1, Juan Manuel Carreño1, Gagandeep Singh A1, Gagandeep Singh B1,2, Michael Schotsaert1,2, Ignacio Mena1,2, Stephen McCroskery1, Lynda Coughlan3,4, Florian Krammer1,5, Adolfo García-Sastre1,2,5,6,7, Peter Palese1,6, Weina Sun1.
Abstract
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.Entities:
Year: 2022 PMID: 35350201 PMCID: PMC8963686 DOI: 10.1101/2022.03.21.485247
Source DB: PubMed Journal: bioRxiv