Q3 · MEDICINE
ArticleOA
Author: Tipper, Jennifer L. ; Killian, John T. ; Brien, James D. ; Green, Todd J. ; Harrod, Kevin S. ; Simpler, Thomas S. ; Mousseau, Betty ; Lee, Young ; Suschak, John J. ; Zhou, Fen ; Dean, Brittany ; Randall, Troy D. ; Zumaquero, Esther ; Peel, Jessica N. ; Risley, Christopher A. ; Allie, S. Rameeza ; Zhang, Jianfeng ; Yang, Guang ; Botta, Davide ; Krishnan, Vyjayanthi ; Lund, Frances E. ; Schultz, Michael D. ; Dickson, Alexandria M. ; Bradley, John E. ; King, R. Glenn ; Peguillet, Isabelle ; Roberts, M. Scot ; Feng, Tsungwei ; Liu, Mingyong ; Shang, Qiao ; Georges, Bertrand ; Qiu, Shihong ; Pinto, Amelia K. ; Shiberu, Bethlehem ; Silva-Sanchez, Aaron ; Meza-Perez, Selene
The coronavirus disease 2019 (COVID-19) pandemic has highlighted the urgent need for effective prophylactic vaccination to prevent the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Intranasal vaccination is an attractive strategy to prevent COVID-19 as the nasal mucosa represents the first-line barrier to SARS-CoV-2 entry. The current intramuscular vaccines elicit systemic immunity but not necessarily high-level mucosal immunity. Here, we tested a single intranasal dose of our candidate adenovirus type 5-vectored vaccine encoding the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein (AdCOVID) in inbred, outbred, and transgenic mice. A single intranasal vaccination with AdCOVID elicited a strong and focused immune response against RBD through the induction of mucosal IgA in the respiratory tract, serum neutralizing antibodies, and CD4+ and CD8+ T cells with a Th1-like cytokine expression profile. A single AdCOVID dose resulted in immunity that was sustained for over six months. Moreover, a single intranasal dose completely protected K18-hACE2 mice from lethal SARS-CoV-2 challenge, preventing weight loss and mortality. These data show that AdCOVID promotes concomitant systemic and mucosal immunity and represents a promising vaccine candidate.