2区 · 医学
Article
作者: Joag, Vineet ; Mickelson, Clayton K ; Bold, Tyler D ; Langlois, Ryan A ; Stolley, J Michael ; Walter, Jennifer A ; Quarnstrom, Clare F ; Thiede, Joshua M ; Jenkins, Marc K ; Becker, Samuel ; Wijeyesinghe, Sathi ; Vezys, Vaiva ; Masopust, David ; Weyu, Eyob ; Vu, Michelle N ; Matchett, William E ; Shepherd, Frances K ; O’Flanagan, Stephen D ; Menachery, Vineet D ; Soerens, Andrew G
AbstractSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the COVID-19 pandemic. Neutralizing Abs target the receptor binding domain of the spike (S) protein, a focus of successful vaccine efforts. Concerns have arisen that S-specific vaccine immunity may fail to neutralize emerging variants. We show that vaccination with a human adenovirus type 5 vector expressing the SARS-CoV-2 nucleocapsid (N) protein can establish protective immunity, defined by reduced weight loss and viral load, in both Syrian hamsters and K18-hACE2 mice. Challenge of vaccinated mice was associated with rapid N-specific T cell recall responses in the respiratory mucosa. This study supports the rationale for including additional viral Ags in SARS-CoV-2 vaccines, even if they are not a target of neutralizing Abs, to broaden epitope coverage and immune effector mechanisms.