Your browser doesn't support javascript.
loading
Trivalent NDV-HXP-S vaccine protects against phylogenetically distant SARS-CoV-2 variants of concern in mice
Irene González-Domínguez; Jose Luis Martínez; Stefan Slamanig; Nicholas Lemus; Yonghong Liu; Tsoi Ying Lai; Juan Manuel Carreno; Gagandeep Singh; Gagandeep Singh; Michael Schotsaert; Ignacio Mena; Stephen McCroskery; Lynda Coughlan; Florian Krammer; Adolfo García-Sastre; Peter Palese; Weina Sun.
Affiliation
  • Irene González-Domínguez; Icahn School of Medicine at Mount Sinai
  • Jose 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 Carreno; 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; Mount Sinai School of Medicine
  • Stephen McCroskery; Icahn School of Medicine at Mount Sinai
  • Lynda Coughlan; University of Maryland School of Medicine
  • 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
Preprint de En | PREPRINT-BIORXIV | ID: ppbiorxiv-485247
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.
Licence
cc_by_nc_nd
Texte intégral: 1 Collection: 09-preprints Base de données: PREPRINT-BIORXIV Type d'étude: Rct Langue: En Année: 2022 Type de document: Preprint
Texte intégral: 1 Collection: 09-preprints Base de données: PREPRINT-BIORXIV Type d'étude: Rct Langue: En Année: 2022 Type de document: Preprint