Back to Search Start Over

Breadth of SARS-CoV-2 neutralization and protection induced by a nanoparticle vaccine.

Authors :
Li D
Martinez DR
Schäfer A
Chen H
Barr M
Sutherland LL
Lee E
Parks R
Mielke D
Edwards W
Newman A
Bock KW
Minai M
Nagata BM
Gagne M
Douek DC
DeMarco CT
Denny TN
Oguin TH 3rd
Brown A
Rountree W
Wang Y
Mansouri K
Edwards RJ
Ferrari G
Sempowski GD
Eaton A
Tang J
Cain DW
Santra S
Pardi N
Weissman D
Tomai MA
Fox CB
Moore IN
Andersen H
Lewis MG
Golding H
Seder R
Khurana S
Baric RS
Montefiori DC
Saunders KO
Haynes BF
Source :
Nature communications [Nat Commun] 2022 Oct 23; Vol. 13 (1), pp. 6309. Date of Electronic Publication: 2022 Oct 23.
Publication Year :
2022

Abstract

Coronavirus vaccines that are highly effective against current and anticipated SARS-CoV-2 variants are needed to control COVID-19. We previously reported a receptor-binding domain (RBD)-sortase A-conjugated ferritin nanoparticle (scNP) vaccine that induced neutralizing antibodies against SARS-CoV-2 and pre-emergent sarbecoviruses and protected non-human primates (NHPs) from SARS-CoV-2 WA-1 infection. Here, we find the RBD-scNP induced neutralizing antibodies in NHPs against pseudoviruses of SARS-CoV and SARS-CoV-2 variants including 614G, Beta, Delta, Omicron BA.1, BA.2, BA.2.12.1, and BA.4/BA.5, and a designed variant with escape mutations, PMS20. Adjuvant studies demonstrate variant neutralization titers are highest with 3M-052-aqueous formulation (AF). Immunization twice with RBD-scNPs protect NHPs from SARS-CoV-2 WA-1, Beta, and Delta variant challenge, and protect mice from challenges of SARS-CoV-2 Beta variant and two other heterologous sarbecoviruses. These results demonstrate the ability of RBD-scNPs to induce broad neutralization of SARS-CoV-2 variants and to protect animals from multiple different SARS-related viruses. Such a vaccine could provide broad immunity to SARS-CoV-2 variants.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
36274085
Full Text :
https://doi.org/10.1038/s41467-022-33985-4