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A COVID-19 vaccine candidate using SpyCatcher multimerization of the SARS-CoV-2 spike protein receptor-binding domain induces potent neutralising antibody responses.

Authors :
Tan TK
Rijal P
Rahikainen R
Keeble AH
Schimanski L
Hussain S
Harvey R
Hayes JWP
Edwards JC
McLean RK
Martini V
Pedrera M
Thakur N
Conceicao C
Dietrich I
Shelton H
Ludi A
Wilsden G
Browning C
Zagrajek AK
Bialy D
Bhat S
Stevenson-Leggett P
Hollinghurst P
Tully M
Moffat K
Chiu C
Waters R
Gray A
Azhar M
Mioulet V
Newman J
Asfor AS
Burman A
Crossley S
Hammond JA
Tchilian E
Charleston B
Bailey D
Tuthill TJ
Graham SP
Duyvesteyn HME
Malinauskas T
Huo J
Tree JA
Buttigieg KR
Owens RJ
Carroll MW
Daniels RS
McCauley JW
Stuart DI
Huang KA
Howarth M
Townsend AR
Source :
Nature communications [Nat Commun] 2021 Jan 22; Vol. 12 (1), pp. 542. Date of Electronic Publication: 2021 Jan 22.
Publication Year :
2021

Abstract

There is need for effective and affordable vaccines against SARS-CoV-2 to tackle the ongoing pandemic. In this study, we describe a protein nanoparticle vaccine against SARS-CoV-2. The vaccine is based on the display of coronavirus spike glycoprotein receptor-binding domain (RBD) on a synthetic virus-like particle (VLP) platform, SpyCatcher003-mi3, using SpyTag/SpyCatcher technology. Low doses of RBD-SpyVLP in a prime-boost regimen induce a strong neutralising antibody response in mice and pigs that is superior to convalescent human sera. We evaluate antibody quality using ACE2 blocking and neutralisation of cell infection by pseudovirus or wild-type SARS-CoV-2. Using competition assays with a monoclonal antibody panel, we show that RBD-SpyVLP induces a polyclonal antibody response that recognises key epitopes on the RBD, reducing the likelihood of selecting neutralisation-escape mutants. Moreover, RBD-SpyVLP is thermostable and can be lyophilised without losing immunogenicity, to facilitate global distribution and reduce cold-chain dependence. The data suggests that RBD-SpyVLP provides strong potential to address clinical and logistic challenges of the COVID-19 pandemic.

Details

Language :
English
ISSN :
2041-1723
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
33483491
Full Text :
https://doi.org/10.1038/s41467-020-20654-7