PropertyValue
?:abstract
  • Understanding the hallmarks of the immune response to SARS-CoV-2 is critical for fighting the COVID-19 pandemic. We assessed antibody and T cell reactivity in convalescent COVID-19 patients and healthy donors sampled both prior to and during the pandemic. Healthy donors examined during the pandemic exhibited increased numbers of SARS-CoV-2-specific T cells, but no humoral response. Their probable exposure to the virus resulted in either asymptomatic infection without antibody secretion, or activation of pre-existing immunity. In convalescent patients, we observed a public and diverse T cell response to SARS-CoV-2 epitopes, revealing T cell receptor (TCR) motifs with germline-encoded features. Bulk CD4+ and CD8+ T cell responses to the spike glycoprotein were mediated by groups of homologous TCRs, some of them shared across multiple donors. Overall, our results demonstrate that the T cell response to SARS-CoV-2, including the identified set of TCRs, can serve as a useful biomarker for surveying antiviral immunity.
is ?:annotates of
?:creator
?:doi
?:doi
  • 10.1016/j.immuni.2020.11.004
?:journal
  • Immunity
?:license
  • els-covid
?:pdf_json_files
  • document_parses/pdf_json/bbe9788d0a73dd068ad4b6dbb8b9f2c75d036974.json
?:pmcid
?:pmid
?:pmid
  • 33326767.0
?:publication_isRelatedTo_Disease
is ?:relation_isRelatedTo_publication of
?:sha_id
?:source
  • Elsevier; Medline; PMC
?:title
  • SARS-CoV-2 epitopes are recognized by a public and diverse repertoire of human T cell receptors
?:type
?:year
  • 2020-11-13

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