A COVID-19 vaccine candidate using SpyCatcher multimerization of the SARS-CoV-2 spike protein receptor-binding domain induces potent neutralising antibody responses.
Angiotensin-Converting Enzyme 2
/ immunology
Animals
Antibodies, Blocking
/ immunology
Antibodies, Monoclonal
/ immunology
Antibodies, Neutralizing
/ immunology
Antibodies, Viral
/ immunology
COVID-19
/ immunology
COVID-19 Vaccines
/ immunology
Cell Line
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Peptides
/ immunology
Protein Interaction Domains and Motifs
Protein Multimerization
SARS-CoV-2
/ immunology
Spike Glycoprotein, Coronavirus
/ immunology
Swine
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
22 01 2021
22 01 2021
Historique:
received:
31
08
2020
accepted:
10
12
2020
entrez:
23
1
2021
pubmed:
24
1
2021
medline:
2
2
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 33483491
doi: 10.1038/s41467-020-20654-7
pii: 10.1038/s41467-020-20654-7
pmc: PMC7822889
doi:
Substances chimiques
Antibodies, Blocking
0
Antibodies, Monoclonal
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
COVID-19 Vaccines
0
Peptides
0
Spike Glycoprotein, Coronavirus
0
SpyCatcher peptide
0
SpyTag peptide
0
spike protein, SARS-CoV-2
0
ACE2 protein, human
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
542Subventions
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007039
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 26752
Pays : United Kingdom
Organisme : Wellcome Trust
ID : FC001030
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007037
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C20724/A14414
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007034
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P021336/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : FC001030
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C20724/A26752
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N00065X/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007031
Pays : United Kingdom
Organisme : Cancer Research UK
ID : FC001030
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V001329/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BBS/E/I/00007038
Pays : United Kingdom
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