PropertyValue
?:abstract
  • Subunit vaccines induce immunity to a pathogen by presenting a component of the pathogen and thus inherently limit the representation of pathogen peptides for cellular immunity based memory. We find that SARS-CoV-2 subunit peptides may not be robustly displayed by the Major Histocompatibility Complex (MHC) molecules in certain individuals. We introduce an augmentation strategy for subunit vaccines that adds a small number of SARS-CoV-2 peptides to a vaccine to improve the population coverage of pathogen peptide display. Our population coverage estimates integrate clinical data on peptide immunogenicity in convalescent COVID-19 patients and machine learning predictions. We evaluate the population coverage of 9 different subunits of SARS-CoV-2, including 5 functional domains and 4 full proteins, and augment each of them to fill a predicted coverage gap.
is ?:annotates of
?:creator
?:doi
?:doi
  • 10.1016/j.cels.2020.11.010
?:journal
  • Cell_Syst
?:license
  • els-covid
?:pdf_json_files
  • document_parses/pdf_json/2a56e164dae75a2bd6126dd3240e77bec4e0eed9.json
?:pmcid
?:pmid
?:pmid
  • 33321075.0
?:publication_isRelatedTo_Disease
?:sha_id
?:source
  • Elsevier; Medline; PMC
?:title
  • Predicted Cellular Immunity Population Coverage Gaps for SARS-CoV-2 Subunit Vaccines and their Augmentation by Compact Peptide Sets
?:type
?:year
  • 2020-11-27

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