Children develop robust and sustained cross-reactive spike-specific immune responses to SARS-CoV-2 infection
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Published:2021-12-22
Issue:1
Volume:23
Page:40-49
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ISSN:1529-2908
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Container-title:Nature Immunology
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language:en
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Short-container-title:Nat Immunol
Author:
Dowell Alexander C.ORCID, Butler Megan S., Jinks Elizabeth, Tut Gokhan, Lancaster TaraORCID, Sylla Panagiota, Begum Jusnara, Bruton Rachel, Pearce HaydenORCID, Verma Kriti, Logan Nicola, Tyson GraceORCID, Spalkova Eliska, Margielewska-Davies Sandra, Taylor Graham S.ORCID, Syrimi Eleni, Baawuah Frances, Beckmann Joanne, Okike Ifeanyichukwu O., Ahmad Shazaad, Garstang JoannaORCID, Brent Andrew J., Brent Bernadette, Ireland Georgina, Aiano Felicity, Amin-Chowdhury Zahin, Jones Samuel, Borrow RayORCID, Linley EzraORCID, Wright John, Azad Rafaq, Waiblinger Dagmar, Davis Chris, Thomson Emma C.ORCID, Palmarini Massimo, Willett Brian J.ORCID, Barclay Wendy S., Poh JohnORCID, Amirthalingam Gayatri, Brown Kevin E., Ramsay Mary E.ORCID, Zuo JianminORCID, Moss PaulORCID, Ladhani Shamez
Abstract
AbstractSARS-CoV-2 infection is generally mild or asymptomatic in children but a biological basis for this outcome is unclear. Here we compare antibody and cellular immunity in children (aged 3–11 years) and adults. Antibody responses against spike protein were high in children and seroconversion boosted responses against seasonal Beta-coronaviruses through cross-recognition of the S2 domain. Neutralization of viral variants was comparable between children and adults. Spike-specific T cell responses were more than twice as high in children and were also detected in many seronegative children, indicating pre-existing cross-reactive responses to seasonal coronaviruses. Importantly, children retained antibody and cellular responses 6 months after infection, whereas relative waning occurred in adults. Spike-specific responses were also broadly stable beyond 12 months. Therefore, children generate robust, cross-reactive and sustained immune responses to SARS-CoV-2 with focused specificity for the spike protein. These findings provide insight into the relative clinical protection that occurs in most children and might help to guide the design of pediatric vaccination regimens.
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Reference39 articles.
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