Trivalent NDV-HXP-S Vaccine Protects against Phylogenetically Distant SARS-CoV-2 Variants of Concern in Mice

Irene González‐Domínguez(Icahn School of Medicine at Mount Sinai), José Luis Martínez(Icahn School of Medicine at Mount Sinai), Stefan Slamanig(Icahn School of Medicine at Mount Sinai), Nicholas Lemus(Icahn School of Medicine at Mount Sinai), Yonghong Liu(Icahn School of Medicine at Mount Sinai), Tsoi Ying Lai(Icahn School of Medicine at Mount Sinai), Juan Manuel Carreño(Icahn School of Medicine at Mount Sinai), Gagandeep Singh(Icahn School of Medicine at Mount Sinai), Gagandeep Singh(Icahn School of Medicine at Mount Sinai), Michael Schotsaert(Icahn School of Medicine at Mount Sinai), Ignacio Mena(Icahn School of Medicine at Mount Sinai), Stephen McCroskery(Icahn School of Medicine at Mount Sinai), Lynda Coughlan(University of Maryland, Baltimore), 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), Weina Sun(Icahn School of Medicine at Mount Sinai)
Microbiology Spectrum
June 6, 2022
Cited by 41Open Access
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Abstract

This manuscript describes an extended work on the Newcastle disease virus (NDV)-based vaccine focusing on multivalent formulations of NDV vectors expressing different prefusion-stabilized versions of the spike proteins of different SARS-CoV-2 variants of concern (VOC). We demonstrate here that this low-cost NDV platform can be easily adapted to construct vaccines against SARS-CoV-2 variants. Importantly, 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. We believe that these findings will help to guide efforts for pandemic preparedness against new variants in the future.


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