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Healthy donor T cell responses to common cold coronaviruses and SARS-CoV-2.
Woldemeskel, Bezawit A; Kwaa, Abena K; Garliss, Caroline C; Laeyendecker, Oliver; Ray, Stuart C; Blankson, Joel N.
  • Woldemeskel BA; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Kwaa AK; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Garliss CC; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Laeyendecker O; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Ray SC; Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Baltimore, Maryland, USA.
  • Blankson JN; Department of Medicine, School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
J Clin Invest ; 130(12): 6631-6638, 2020 12 01.
Article in English | MEDLINE | ID: covidwho-1112391
ABSTRACT
BACKGROUNDT cell responses to the common cold coronaviruses have not been well characterized. Preexisting T cell immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been reported, and a recent study suggested that this immunity was due to cross-recognition of the novel coronavirus by T cells specific for the common cold coronaviruses.METHODSWe used the enzyme-linked immunospot (ELISPOT) assay to characterize the T cell responses against peptide pools derived from the spike protein of 3 common cold coronaviruses (HCoV-229E, HCoV-NL63, and HCoV-OC43) and SARS-CoV-2 in 21 healthy donors (HDs) who were seronegative for SARS-CoV-2 and had no known exposure to the virus. An in vitro expansion culture assay was also used to analyze memory T cell responses.RESULTSWe found responses to the spike protein of the 3 common cold coronaviruses in many of the donors. We then focused on HCoV-NL63 and detected broad T cell responses to the spike protein and identified 22 targeted peptides. Interestingly, only 1 study participant had a significant response to SARS-CoV-2 spike or nucleocapsid protein in the ELISPOT assay. In vitro expansion studies suggested that T cells specific for the HCoV-NL63 spike protein in this individual could also recognize SARS-CoV-2 spike protein peptide pools.CONCLUSIONHDs have circulating T cells specific for the spike proteins of HCoV-NL63, HCoV-229E, and HCoV-OC43. T cell responses to SARS-CoV-2 spike and nucleocapsid proteins were present in only 1 participant and were potentially the result of cross-recognition by T cells specific for the common cold coronaviruses. Further studies are needed to determine whether this cross-recognition influences coronavirus disease 2019 (COVID-19) outcomes.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Common Cold / Coronavirus 229E, Human / Coronavirus OC43, Human / Coronavirus NL63, Human / SARS-CoV-2 / COVID-19 / Immunity, Cellular Type of study: Randomized controlled trials Limits: Adult / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article Affiliation country: JCI143120

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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Common Cold / Coronavirus 229E, Human / Coronavirus OC43, Human / Coronavirus NL63, Human / SARS-CoV-2 / COVID-19 / Immunity, Cellular Type of study: Randomized controlled trials Limits: Adult / Female / Humans / Male / Middle aged Language: English Journal: J Clin Invest Year: 2020 Document Type: Article Affiliation country: JCI143120