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Contribution of SARS-CoV-2 infection preceding COVID-19 mRNA vaccination to generation of cellular and humoral immune responses in children.
- Source :
-
Frontiers in immunology [Front Immunol] 2023 Dec 20; Vol. 14, pp. 1327875. Date of Electronic Publication: 2023 Dec 20 (Print Publication: 2023). - Publication Year :
- 2023
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Abstract
- Primary COVID-19 vaccination for children, 5-17 years of age, was offered in the Netherlands at a time when a substantial part of this population had already experienced a SARS-CoV-2 infection. While vaccination has been shown effective, underlying immune responses have not been extensively studied. We studied immune responsiveness to one and/or two doses of primary BNT162b2 mRNA vaccination and compared the humoral and cellular immune response in children with and without a preceding infection. Antibodies targeting the original SARS-CoV-2 Spike or Omicron Spike were measured by multiplex immunoassay. B-cell and T-cell responses were investigated using enzyme-linked immunosorbent spot (ELISpot) assays. The activation of CD4 <superscript>+</superscript> and CD8 <superscript>+</superscript> T cells was studied by flowcytometry. Primary vaccination induced both a humoral and cellular adaptive response in naive children. These responses were stronger in those with a history of infection prior to vaccination. A second vaccine dose did not further boost antibody levels in those who previously experienced an infection. Infection-induced responsiveness prior to vaccination was mainly detected in CD8 <superscript>+</superscript> T cells, while vaccine-induced T-cell responses were mostly by CD4 <superscript>+</superscript> T cells. Thus, SARS-CoV-2 infection prior to vaccination enhances adaptive cellular and humoral immune responses to primary COVID-19 vaccination in children. As most children are now expected to contract infection before the age of five, the impact of infection-induced immunity in children is of high relevance. Therefore, considering natural infection as a priming immunogen that enhances subsequent vaccine-responsiveness may help decision-making on the number and timing of vaccine doses.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2023 Verheul, Vos, de Rond, De Zeeuw-Brouwer, Nijhof, Smit, Oomen, Molenaar, Bogaard, van Bergen, Middelhof, Beckers, Wijmenga-Monsuur, Buisman, Boer, van Binnendijk, de Wit and Guichelaar.)
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 14
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 38193077
- Full Text :
- https://doi.org/10.3389/fimmu.2023.1327875