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[Preprint]. 2020 Oct 11:2020.10.10.331348. [Version 1] doi: 10.1101/2020.10.10.331348

Single-dose intranasal administration of AdCOVID elicits systemic and mucosal immunity against SARS-CoV-2 in mice

Rodney G King, Aaron Silva-Sanchez, Jessica N Peel, Davide Botta, Selene Meza-Perez, Rameeza Allie, Michael D Schultz, Mingyong Liu, John E Bradley, Shihong Qiu, Guang Yang, Fen Zhou, Esther Zumaquero, Thomas S Simpler, Betty Mousseau, John T Killian, Brittany Dean, Qiao Shang, Jennifer L Tipper, Christopher Risley, Kevin S Harrod, Ray Feng, Young Lee, Bethlehem Shiberu, Vyjayanthi Krishnan, Isabelle Peguillet, Jianfeng Zhang, Todd Green, Troy D Randall, Bertrand Georges, Frances E Lund, Scot Roberts
PMCID: PMC7553185  PMID: 33052351

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has highlighted the urgent need for effective preventive vaccination to reduce burden and spread of severe acute respiratory syndrome (SARS) coronavirus 2 (SARS-CoV-2) in humans. Intranasal vaccination is an attractive strategy to prevent COVID-19 as the nasal mucosa represents the first-line barrier to SARS-CoV-2 entry before viral spread to the lung. Although SARS-CoV-2 vaccine development is rapidly progressing, the current intramuscular vaccines are designed to elicit systemic immunity without conferring mucosal immunity. Here, we show that AdCOVID, an intranasal adenovirus type 5 (Ad5)-vectored vaccine encoding the receptor binding domain (RBD) of the SARS-CoV-2 spike protein, elicits a strong and focused immune response against RBD through the induction of mucosal IgA, serum neutralizing antibodies and CD4+ and CD8+ T cells with a Th1-like cytokine expression profile. Therefore, AdCOVID, which promotes concomitant systemic and local mucosal immunity, represents a promising COVID-19 vaccine candidate.

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