Abstract

There is an urgent need for a safe and protective vaccine to control the global spread of SARS-CoV-2 and prevent COVID-19. Here, we report the immunogenicity and protective efficacy of a SARS-CoV-2 subunit vaccine (NVX-CoV2373) produced from the full-length SARS-CoV-2 spike (S) glycoprotein stabilized in the prefusion conformation. Cynomolgus macaques (Macaca fascicularis) immunized with NVX-CoV2373 and the saponin-based Matrix-M™ adjuvant induced anti-S antibody that was neutralizing and blocked binding to the human angiotensin-converting enzyme 2 (hACE2) receptor. Following intranasal and intratracheal challenge with SARS-CoV-2, immunized macaques were protected against upper and lower infection and pulmonary disease. These results support ongoing phase 1/2 clinical studies of the safety and immunogenicity of NVX-CoV2327 vaccine (NCT04368988).

Keywords

ImmunogenicityVirologyAdjuvantMedicineNeutralizing antibodySevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Nasal administrationAntibodyImmunologyCoronavirus disease 2019 (COVID-19)BiologyVirusInfectious disease (medical specialty)DiseasePathology

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Publication Info

Year
2020
Type
article
Volume
38
Issue
50
Pages
7892-7896
Citations
238
Access
Closed

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Mimi Guebre‐Xabier, Nita Patel, Jing-Hui Tian et al. (2020). NVX-CoV2373 vaccine protects cynomolgus macaque upper and lower airways against SARS-CoV-2 challenge. Vaccine , 38 (50) , 7892-7896. https://doi.org/10.1016/j.vaccine.2020.10.064

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DOI
10.1016/j.vaccine.2020.10.064