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Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations

Human milk contains SARS-CoV-2-specific antibodies after COVID-19 vaccination. These milk antibodies decrease several months post-vaccination. Whether booster immunization restores human milk antibody levels, potentially offering prolonged passive immunity for the infant, remains unknown. In this pr...

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Autores principales: Mulleners, Sien J., Juncker, Hannah G., Ruhé, Eliza J. M., Korosi, Aniko, van Goudoever, Johannes B., van Gils, Marit J., van Keulen, Britt J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875178/
https://www.ncbi.nlm.nih.gov/pubmed/36697496
http://dx.doi.org/10.1038/s42003-023-04455-4
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author Mulleners, Sien J.
Juncker, Hannah G.
Ruhé, Eliza J. M.
Korosi, Aniko
van Goudoever, Johannes B.
van Gils, Marit J.
van Keulen, Britt J.
author_facet Mulleners, Sien J.
Juncker, Hannah G.
Ruhé, Eliza J. M.
Korosi, Aniko
van Goudoever, Johannes B.
van Gils, Marit J.
van Keulen, Britt J.
author_sort Mulleners, Sien J.
collection PubMed
description Human milk contains SARS-CoV-2-specific antibodies after COVID-19 vaccination. These milk antibodies decrease several months post-vaccination. Whether booster immunization restores human milk antibody levels, potentially offering prolonged passive immunity for the infant, remains unknown. In this prospective follow-up study, we investigated the longitudinal SARS-CoV-2-specific antibody response in human milk of 26 lactating women who received a COVID-19 booster dose of an mRNA-based vaccine. Moreover, we evaluated whether the booster-induced human milk antibody response differs for participants who received a similar or different vaccine type in their primary vaccination series. All participants (100%) who received a homologous booster vaccination showed SARS-CoV-2-specific immunoglobulin A (IgA) and immunoglobulin G (IgG) in their milk. Heterologous booster vaccination resulted in milk conversion for 9 (69%) and 13 (100%) participants for IgA and IgG respectively. Findings of this study indicate that both homologous and heterologous boosting schedules have the potential to enhance SARS-CoV-2-specific IgA and IgG in human milk.
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spelling pubmed-98751782023-01-25 Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations Mulleners, Sien J. Juncker, Hannah G. Ruhé, Eliza J. M. Korosi, Aniko van Goudoever, Johannes B. van Gils, Marit J. van Keulen, Britt J. Commun Biol Article Human milk contains SARS-CoV-2-specific antibodies after COVID-19 vaccination. These milk antibodies decrease several months post-vaccination. Whether booster immunization restores human milk antibody levels, potentially offering prolonged passive immunity for the infant, remains unknown. In this prospective follow-up study, we investigated the longitudinal SARS-CoV-2-specific antibody response in human milk of 26 lactating women who received a COVID-19 booster dose of an mRNA-based vaccine. Moreover, we evaluated whether the booster-induced human milk antibody response differs for participants who received a similar or different vaccine type in their primary vaccination series. All participants (100%) who received a homologous booster vaccination showed SARS-CoV-2-specific immunoglobulin A (IgA) and immunoglobulin G (IgG) in their milk. Heterologous booster vaccination resulted in milk conversion for 9 (69%) and 13 (100%) participants for IgA and IgG respectively. Findings of this study indicate that both homologous and heterologous boosting schedules have the potential to enhance SARS-CoV-2-specific IgA and IgG in human milk. Nature Publishing Group UK 2023-01-25 /pmc/articles/PMC9875178/ /pubmed/36697496 http://dx.doi.org/10.1038/s42003-023-04455-4 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mulleners, Sien J.
Juncker, Hannah G.
Ruhé, Eliza J. M.
Korosi, Aniko
van Goudoever, Johannes B.
van Gils, Marit J.
van Keulen, Britt J.
Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title_full Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title_fullStr Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title_full_unstemmed Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title_short Comparing the SARS-CoV-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
title_sort comparing the sars-cov-2-specific antibody response in human milk after homologous and heterologous booster vaccinations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9875178/
https://www.ncbi.nlm.nih.gov/pubmed/36697496
http://dx.doi.org/10.1038/s42003-023-04455-4
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