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

R. G. King, A. Silva-Sanchez, J. N. Peel, D. Botta, S. Meza-Perez, R. Allie, M. D. Schultz, M. Liu, J. E. Bradley, S. Qiu, G. Yang, F. Zhou, E. Zumaquero, T. S. Simpler, B. Mousseau, J. T. Killian, B. Dean, Q. Shang, J. L. Tipper, C. Risley, K. S. Harrod, R. Feng, Y. Lee, B. Shiberu, V. Krishnan, , S. Roberts

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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