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Characterization of SARS-CoV-2 and common cold coronavirus-specific T-cell responses in MIS-C and Kawasaki disease children.

Abstract
The immunopathogenesis of multisystem inflammatory syndrome (MIS-C) in children that may follow exposure to SARS-CoV-2 is incompletely understood. Here, we studied SARS-CoV-2-specific T cells in MIS-C, Kawasaki disease (KD), and SARS-CoV-2 convalescent controls using peptide pools derived from SARS-CoV-2 spike or nonspike proteins, and common cold coronaviruses (CCC). Coordinated CD4+ and CD8+ SARS-CoV-2-specific T cells were detected in five MIS-C subjects with cross-reactivity to CCC. CD4+ and CD8+ T-cell responses alone were documented in three and one subjects, respectively. T-cell specificities in MIS-C did not correlate with disease severity and were similar to SARS-CoV-2 convalescent controls. T-cell memory and cross-reactivity to CCC in MIS-C and SARS-CoV-2 convalescent controls were also similar. The chemokine receptor CCR6, but not CCR9, was highly expressed on SARS-CoV-2-specific CD4+ but not on CD8+ T cells. Only two of 10 KD subjects showed a T-cell response to CCC. Enumeration of myeloid APCs revealed low cell precursors in MIS-C subjects compared to KD. In summary, children with MIS-C mount a normal T-cell response to SARS-CoV-2 with no apparent relationship to antecedent CCC exposure. Low numbers of tolerogenic myeloid DCs may impair their anti-inflammatory response.
AuthorsLi-En Hsieh, Alba Grifoni, John Sidney, Chisato Shimizu, Hiroko Shike, Nanda Ramchandar, Elizabeth Moreno, Adriana H Tremoulet, Jane C Burns, Alessandra Franco
JournalEuropean journal of immunology (Eur J Immunol) Vol. 52 Issue 1 Pg. 123-137 (01 2022) ISSN: 1521-4141 [Electronic] Germany
PMID34599760 (Publication Type: Clinical Trial, Journal Article, Research Support, N.I.H., Extramural)
Copyright© 2021 The Authors. European Journal of Immunology published by Wiley-VCH GmbH.
Topics
  • Adolescent
  • CD4-Positive T-Lymphocytes (immunology)
  • CD8-Positive T-Lymphocytes (immunology)
  • COVID-19 (complications, immunology)
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Immunity, Cellular
  • Immunologic Memory
  • Infant
  • Male
  • Mucocutaneous Lymph Node Syndrome (complications, immunology)
  • SARS-CoV-2 (immunology)
  • Systemic Inflammatory Response Syndrome (immunology)

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