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Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19

Author

Listed:
  • Shidan Tosif

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    The Royal Children’s Hospital)

  • Melanie R. Neeland

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Philip Sutton

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Paul V. Licciardi

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Sohinee Sarkar

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Kevin J. Selva

    (The University of Melbourne)

  • Lien Anh Ha Do

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Celeste Donato

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Zheng Quan Toh

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Rachel Higgins

    (Infection and Immunity, Murdoch Children’s Research Institute)

  • Carolien Van de Sandt

    (The University of Melbourne
    Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam)

  • Melissa M. Lemke

    (University of Michigan)

  • Christina Y. Lee

    (University of Michigan)

  • Suzanne K. Shoffner

    (University of Michigan)

  • Katie L. Flanagan

    (Launceston General Hospital
    University of Tasmania
    Monash University
    RMIT University)

  • Kelly B. Arnold

    (University of Michigan)

  • Francesca L. Mordant

    (The University of Melbourne)

  • Kim Mulholland

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    Infectious Diseases Unit, Department of General Medicine, The Royal Children’s Hospital)

  • Julie Bines

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    Department of Gastroenterology, The Royal Children’s Hospital)

  • Kate Dohle

    (Infection and Immunity, Murdoch Children’s Research Institute)

  • Daniel G. Pellicci

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Nigel Curtis

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    Infectious Diseases Unit, Department of General Medicine, The Royal Children’s Hospital)

  • Sarah McNab

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    The Royal Children’s Hospital)

  • Andrew Steer

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    Infectious Diseases Unit, Department of General Medicine, The Royal Children’s Hospital)

  • Richard Saffery

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute)

  • Kanta Subbarao

    (The University of Melbourne
    WHO Collaborating Centre for Reference and Research on Influenza)

  • Amy W. Chung

    (The University of Melbourne)

  • Katherine Kedzierska

    (The University of Melbourne)

  • David P. Burgner

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    Infectious Diseases Unit, Department of General Medicine, The Royal Children’s Hospital)

  • Nigel W. Crawford

    (The University of Melbourne
    Infection and Immunity, Murdoch Children’s Research Institute
    The Royal Children’s Hospital)

Abstract

Compared to adults, children with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have predominantly mild or asymptomatic infections, but the underlying immunological differences remain unclear. Here, we describe clinical features, virology, longitudinal cellular, and cytokine immune profile, SARS-CoV-2-specific serology and salivary antibody responses in a family of two parents with PCR-confirmed symptomatic SARS-CoV-2 infection and their three children, who tested repeatedly SARS-CoV-2 PCR negative. Cellular immune profiles and cytokine responses of all children are similar to their parents at all timepoints. All family members have salivary anti-SARS-CoV-2 antibodies detected, predominantly IgA, that coincide with symptom resolution in 3 of 4 symptomatic members. Plasma from both parents and one child have IgG antibody against the S1 protein and virus-neutralizing activity detected. Using a systems serology approach, we demonstrate higher levels of SARS-CoV-2-specific antibody features of these family members compared to healthy controls. These data indicate that children can mount an immune response to SARS-CoV-2 without virological confirmation of infection, raising the possibility that immunity in children can prevent the establishment of SARS-CoV-2 infection. Relying on routine virological and serological testing may not identify exposed children, with implications for epidemiological and clinical studies across the life-span.

Suggested Citation

  • Shidan Tosif & Melanie R. Neeland & Philip Sutton & Paul V. Licciardi & Sohinee Sarkar & Kevin J. Selva & Lien Anh Ha Do & Celeste Donato & Zheng Quan Toh & Rachel Higgins & Carolien Van de Sandt & Me, 2020. "Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19," Nature Communications, Nature, vol. 11(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19545-8
    DOI: 10.1038/s41467-020-19545-8
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    Cited by:

    1. Tejas Menon & Patricia T. Illing & Priyanka Chaurasia & Hayley A. McQuilten & Chloe Shepherd & Louise C. Rowntree & Jan Petersen & Dene R. Littler & Grace Khuu & Ziyi Huang & Lilith F. Allen & Steve R, 2024. "CD8+ T-cell responses towards conserved influenza B virus epitopes across anatomical sites and age," Nature Communications, Nature, vol. 15(1), pages 1-21, December.

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