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A single intranasal dose of chimpanzee adenovirus-vectored vaccine protects against SARS-CoV-2 infection in rhesus macaques

Authors :
Jamie Lovaglio
Julie Callison
Ahmed O. Hassan
Michael S. Diamond
Patrick W. Hanley
David T. Curiel
Haiyan Zhao
Rita E. Chen
Daved H. Fremont
Atsushi Okumura
James Brett Case
Kimberly Meade-White
Friederike Feldmann
Dana P. Scott
Heinz Feldmann
Tsing Lee Tang-Huau
Source :
Cell Reports Medicine, Vol 2, Iss 4, Pp 100230-(2021), Cell Reports Medicine, bioRxiv
Publication Year :
2021
Publisher :
Elsevier, 2021.

Abstract

The deployment of a vaccine that limits transmission and disease likely will be required to end the Coronavirus Disease 2019 (COVID-19) pandemic. We recently described the protective activity of an intranasally-administered chimpanzee adenovirus-vectored vaccine encoding a pre-fusion stabilized spike (S) protein (ChAd-SARS-CoV-2-S) in the upper and lower respiratory tract of mice expressing the human angiotensin-converting enzyme 2 (ACE2) receptor. Here, we show the immunogenicity and protective efficacy of this vaccine in non-human primates. Rhesus macaques were immunized with ChAd-Control or ChAd-SARS-CoV-2-S and challenged one month later by combined intranasal and intrabronchial routes with SARS-CoV-2. A single intranasal dose of ChAd-SARS-CoV-2-S induces neutralizing antibodies and T cell responses and limits or prevents infection in the upper and lower respiratory tract after SARS-CoV-2 challenge. As this single intranasal dose vaccine confers protection against SARS-CoV-2 in non-human primates, it is a promising candidate for limiting SARS-CoV-2 infection and transmission in humans.<br />Graphical Abstract<br />Hassan et al show that a single dose immunization of rhesus monkeys with ChAd-SARS-CoV-2-S via an intranasal route induces neutralizing antibodies and T cell responses against SARS-CoV-2. ChAd-SARS-CoV-2-S vaccine protects rhesus monkeys against SARS-CoV-2 infection in both the upper and lower respiratory tracts.

Details

Language :
English
ISSN :
26663791
Volume :
2
Issue :
4
Database :
OpenAIRE
Journal :
Cell Reports Medicine
Accession number :
edsair.doi.dedup.....04d9bc020cbff5ee83f2c6ef16878b99