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Immunity ; 53(6): 1245-1257.e5, 2020 12 15.
Article in English | MEDLINE | ID: covidwho-922005

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 preexisting 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 protein 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.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , COVID-19/immunology , Epitopes, T-Lymphocyte/metabolism , SARS-CoV-2/physiology , Spike Glycoprotein, Coronavirus/metabolism , Adolescent , Adult , Antibodies, Viral/metabolism , Asymptomatic Infections , Cells, Cultured , Convalescence , Epitopes, T-Lymphocyte/immunology , Female , Humans , Immunity , Immunologic Memory , Lymphocyte Activation , Male , Middle Aged , Pandemics , Receptors, Antigen, T-Cell/metabolism , Spike Glycoprotein, Coronavirus/immunology , Young Adult
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