Natural and hybrid immunity after SARS-CoV-2 infection in children and adolescents

  • \(\bf Purpose\) In contrast to adults, immune protection against SARS-CoV-2 in children and adolescents with natural or hybrid immunity is still poorly understood. The aim of this study was to analyze different immune compartments in different age groups and whether humoral immune reactions correlate with a cellular immune response. \(\bf Methods\) 72 children and adolescents with a preceding SARS-CoV-2 infection were recruited. 37 were vaccinated with an RNA vaccine (BNT162b2). Humoral immunity was analyzed 3–26 months (median 10 months) after infection by measuring Spike protein (S), nucleocapsid (NCP), and neutralizing antibodies (nAB). Cellular immunity was analyzed using a SARS-CoV-2-specific interferon-\(\gamma\) release assay (IGRA). \(\bf Results\) All children and adolescents had S antibodies; titers were higher in those with hybrid immunity (14,900 BAU/ml vs. 2118 BAU/ml). NCP antibodies were detectable in > 90%. Neutralizing antibodies (nAB) were more frequently detected (90%) with higher titers (1914 RLU) in adolescents with hybrid immunity than in children with natural immunity (62.5%, 476 RLU). Children with natural immunity were less likely to have reactive IGRAs (43.8%) than adolescents with hybrid immunity (85%). The amount of interferon-\(\gamma\) released by T cells was comparable in natural and hybrid immunity. \(\bf Conclusion\) Spike antibodies are the most reliable markers to monitor an immune reaction against SARS-CoV-2. High antibody titers of spike antibodies and nAB correlated with cellular immunity, a phenomenon found only in adolescents with hybrid immunity. Hybrid immunity is associated with markedly higher antibody titers and a higher probability of a cellular immune response than a natural immunity.

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Author:Friedrich Tobias Ingo RothoeftORCiDGND, Christoph MaierORCiDGND, Adriana TalaricoGND, Anna Teresa HoffmannGND, Anne SchlegtendalORCiDGND, Berit LangeGND, Astrid PetersmannGND, Robin DenzGND, Nina TimmesfeldORCiDGND, Nicole Marina TöpfnerGND, Elena Vidal BlancoGND, Stephanie PfänderORCiDGND, Thomas LückeGND, Folke BrinkmannORCiDGND
URN:urn:nbn:de:hbz:294-113259
DOI:https://doi.org/10.1007/s15010-024-02225-w
Parent Title (English):Infection
Publisher:Springer
Place of publication:Berlin
Document Type:Article
Language:English
Date of Publication (online):2024/10/10
Date of first Publication:2024/03/18
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Antibody; COVID-19; Children; Convalescent; Immunity; SARS-CoV-2; T cell; Vaccination
Volume:52
First Page:1449
Last Page:1458
Note:
Dieser Beitrag ist auf Grund des DEAL-Springer-Vertrages frei zugänglich.
Institutes/Facilities:St. Josef-Hospital Bochum, Klinik für Kinder- und Jugendmedizin
Katholisches Klinikum Bochum, Klinik für Kinder- und Jugendmedizin
Dewey Decimal Classification:Technik, Medizin, angewandte Wissenschaften / Medizin, Gesundheit
open_access (DINI-Set):open_access
Licence (English):License LogoCreative Commons - CC BY 4.0 - Attribution 4.0 International