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About:
Self-amplifying RNA SARS-CoV-2 lipid nanoparticle vaccine candidate induces high neutralizing antibody titers in mice
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Self-amplifying RNA SARS-CoV-2 lipid nanoparticle vaccine candidate induces high neutralizing antibody titers in mice
Creator
Zhou, Jie
Barclay, Wendy
Hu, Kai
Shattock, Robin
Barbosa, Christopher
Blakney, Anna
Bouton, Clément
Brown, Jonathan
Lin, Paulo
Mckay, Paul
Penn, Rebecca
Polra, Krunal
Rogers, Paul
Samnuan, Karnyart
Tam, Ying
Source
Medline; PMC
abstract
The spread of the SARS-CoV-2 into a global pandemic within a few months of onset motivates the development of a rapidly scalable vaccine. Here, we present a self-amplifying RNA encoding the SARS-CoV-2 spike protein encapsulated within a lipid nanoparticle (LNP) as a vaccine. We observe remarkably high and dose-dependent SARS-CoV-2 specific antibody titers in mouse sera, as well as robust neutralization of both a pseudo-virus and wild-type virus. Upon further characterization we find that the neutralization is proportional to the quantity of specific IgG and of higher magnitude than recovered COVID-19 patients. saRNA LNP immunizations induce a Th1-biased response in mice, and there is no antibody-dependent enhancement (ADE) observed. Finally, we observe high cellular responses, as characterized by IFN-γ production, upon re-stimulation with SARS-CoV-2 peptides. These data provide insight into the vaccine design and evaluation of immunogenicity to enable rapid translation to the clinic.
has issue date
2020-07-09
(
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bibo:doi
10.1038/s41467-020-17409-9
bibo:pmid
32647131
has license
cc-by
sha1sum (hex)
6ba5a8ca3f82fcea6002932bafffe1264ca63709
schema:url
https://doi.org/10.1038/s41467-020-17409-9
resource representing a document's title
Self-amplifying RNA SARS-CoV-2 lipid nanoparticle vaccine candidate induces high neutralizing antibody titers in mice
has PubMed Central identifier
PMC7347890
has PubMed identifier
32647131
schema:publication
Nat Commun
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covid:6ba5a8ca3f82fcea6002932bafffe1264ca63709#body_text
is
schema:about
of
named entity 'COVID-19'
named entity 'data'
named entity 'PATIENTS'
named entity 'RECOVERED'
named entity 'ENHANCEMENT'
named entity 'MONTHS'
named entity 'RNA'
named entity 'scalable'
named entity 'sera'
named entity 'vaccine'
named entity 'insight'
named entity 'onset'
named entity 'encapsulated'
named entity 'lipid'
named entity 'Th1'
named entity 'dose-dependent'
named entity 'mice'
named entity 'global pandemic'
named entity 'immunogenicity'
named entity 'LNP'
named entity 'vaccine'
named entity 'SARS-CoV-2'
named entity 'lipid'
named entity 'nanoparticle'
named entity 'SARS-CoV-2'
named entity 'FITC'
named entity '37°C'
named entity 'saRNA'
named entity 'SARS-CoV-2'
named entity 'recombinant'
named entity 'saRNA'
named entity 'pseudovirus'
named entity 'RNA'
named entity 'antibodies'
named entity 'positive control'
named entity 'glycoprotein'
named entity 'MERS-CoV'
named entity 'trimerization'
named entity 'vaccination'
named entity 'LNP'
named entity 'transfection'
named entity 'BALB/c'
named entity 'control group'
named entity 'carbenicillin'
named entity 'SARS-CoV-2'
named entity 'proline'
named entity 'luciferase'
named entity 'humoral'
named entity 'Th1'
named entity 'multiple comparisons'
named entity 'SARS-CoV-2'
named entity 'RANTEs'
named entity 'immune response'
named entity 'lipid'
named entity 'infection'
named entity 'RNA 11'
named entity 'Creative Commons'
named entity 'IgG'
named entity 'immune response'
named entity 'vaccine'
named entity 'plasmid'
named entity 'pseudotyped'
named entity 'LNP'
named entity 'HEPES'
named entity 'protein'
named entity 'Antibody'
named entity 'Thermo Fisher Scientific'
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