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Heterologous Immune Responses of Serum IgG and Secretory IgA Against the Spike Protein of Endemic Coronaviruses During Severe COVID-19

  • Wouter L. Smit
  • , Sophie van Tol
  • , Sanne van der Wal
  • , Femke van Vulpen
  • , Shannon la Grouw
  • , Lenneke van Lelyveld
  • , Gijs Limonard
  • , Ailko Bossink
  • , Gert-Jan Godeke
  • , Sandhya Shrestha
  • , Johan Reimerink
  • , Dirk Eggink
  • , Chantal Reusken
  • , Michiel Heron
  • , Steven Thijsen*
  • *Corresponding author for this work
  • Diakonessenhuis Utrecht
  • University Medical Center Utrecht
  • National Institute of Public Health and the Environment

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Defining immune correlates of disease severity is important to better understand the immunopathogenesis in COVID-19. Here we made use of a protein microarray platform to detect IgG- and IgA-reactive antibodies in sera and saliva respectively, and assess cross-reactivity between SARS-CoV-2 and endemic coronaviruses (eCoVs). IgG responses against the full protein of spike, but not the S1 subunit, were significantly higher in convalescent sera of patients with severe disease compared to mild disease and healthy controls. In addition, we detected reactivity of secretory IgA to eCoVs in saliva of patients with severe disease, not present in patients with moderate disease or seropositive healthy controls. These heterologous immune responses are in line with non-protective cross-reactivity, and support a potential role for immune imprinting in the pathogenesis of severe COVID-19.
Original languageEnglish
Article number839367
JournalFrontiers in immunology
Volume13
DOIs
Publication statusPublished - 9 Mar 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • COVID-19
  • SARS-CoV-2
  • immune imprinting
  • seasonal coronaviruses
  • spike protein

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