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Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein

Immunity induced by vaccination and infection, referred to as hybrid immunity, provides better protection against SARS-CoV-2 infections compared to immunity induced by vaccinations alone. To assess the development of hybrid immunity we investigated the induction of Nucleoprotein-specific antibodies...

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Autores principales: den Hartog, Gerco, Andeweg, Stijn P., Hoeve, Christina E., Smits, Gaby, Voordouw, Bettie, Eggink, Dirk, Knol, Mirjam J., van Binnendijk, Robert S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603038/
https://www.ncbi.nlm.nih.gov/pubmed/37884642
http://dx.doi.org/10.1038/s41598-023-45718-8
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author den Hartog, Gerco
Andeweg, Stijn P.
Hoeve, Christina E.
Smits, Gaby
Voordouw, Bettie
Eggink, Dirk
Knol, Mirjam J.
van Binnendijk, Robert S.
author_facet den Hartog, Gerco
Andeweg, Stijn P.
Hoeve, Christina E.
Smits, Gaby
Voordouw, Bettie
Eggink, Dirk
Knol, Mirjam J.
van Binnendijk, Robert S.
author_sort den Hartog, Gerco
collection PubMed
description Immunity induced by vaccination and infection, referred to as hybrid immunity, provides better protection against SARS-CoV-2 infections compared to immunity induced by vaccinations alone. To assess the development of hybrid immunity we investigated the induction of Nucleoprotein-specific antibodies in PCR-confirmed infections by Delta or Omicron in vaccinated individuals (n = 520). Eighty-two percent of the participants with a breakthrough infection reached N-seropositivity. N-seropositivity was accompanied by Spike S1 antibody boosting, and independent of vaccination status or virus variant. Following the infection relatively more antibodies to the infecting virus variant were detected. In conclusion, these data show that hybrid immunity through breakthrough infections is hallmarked by Nucleoprotein antibodies and broadening of the Spike antibody repertoire. Exposure to future SARS-CoV-2 variants may therefore continue to maintain and broaden vaccine-induced population immunity.
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spelling pubmed-106030382023-10-28 Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein den Hartog, Gerco Andeweg, Stijn P. Hoeve, Christina E. Smits, Gaby Voordouw, Bettie Eggink, Dirk Knol, Mirjam J. van Binnendijk, Robert S. Sci Rep Article Immunity induced by vaccination and infection, referred to as hybrid immunity, provides better protection against SARS-CoV-2 infections compared to immunity induced by vaccinations alone. To assess the development of hybrid immunity we investigated the induction of Nucleoprotein-specific antibodies in PCR-confirmed infections by Delta or Omicron in vaccinated individuals (n = 520). Eighty-two percent of the participants with a breakthrough infection reached N-seropositivity. N-seropositivity was accompanied by Spike S1 antibody boosting, and independent of vaccination status or virus variant. Following the infection relatively more antibodies to the infecting virus variant were detected. In conclusion, these data show that hybrid immunity through breakthrough infections is hallmarked by Nucleoprotein antibodies and broadening of the Spike antibody repertoire. Exposure to future SARS-CoV-2 variants may therefore continue to maintain and broaden vaccine-induced population immunity. Nature Publishing Group UK 2023-10-26 /pmc/articles/PMC10603038/ /pubmed/37884642 http://dx.doi.org/10.1038/s41598-023-45718-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
den Hartog, Gerco
Andeweg, Stijn P.
Hoeve, Christina E.
Smits, Gaby
Voordouw, Bettie
Eggink, Dirk
Knol, Mirjam J.
van Binnendijk, Robert S.
Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title_full Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title_fullStr Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title_full_unstemmed Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title_short Assessment of hybrid population immunity to SARS-CoV-2 following breakthrough infections of distinct SARS-CoV-2 variants by the detection of antibodies to nucleoprotein
title_sort assessment of hybrid population immunity to sars-cov-2 following breakthrough infections of distinct sars-cov-2 variants by the detection of antibodies to nucleoprotein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603038/
https://www.ncbi.nlm.nih.gov/pubmed/37884642
http://dx.doi.org/10.1038/s41598-023-45718-8
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