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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.
- 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.
- Subjects :
- Angiotensin-Converting Enzyme 2 immunology
Animals
Antibodies, Blocking immunology
Antibodies, Monoclonal immunology
Antibodies, Neutralizing immunology
COVID-19 immunology
Cell Line
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Protein Interaction Domains and Motifs
Protein Multimerization
Swine
Antibodies, Viral immunology
COVID-19 prevention & control
COVID-19 Vaccines immunology
Peptides immunology
SARS-CoV-2 immunology
Spike Glycoprotein, Coronavirus immunology
Subjects
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