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Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status

The essential trace element selenium (Se) is of central importance for human health and particularly for a regular functioning of the immune system. In the context of the current pandemic, Se deficiency in patients with COVID-19 correlated with disease severity and mortality risk. Selenium has been...

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Autores principales: Demircan, Kamil, Chillon, Thilo Samson, Sun, Qian, Heller, Raban Arved, Klingenberg, Georg Jochen, Hirschbil-Bremer, Ines Maria, Seemann, Petra, Diegmann, Joachim, Bachmann, Manuel, Moghaddam, Arash, Schomburg, Lutz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810594/
https://www.ncbi.nlm.nih.gov/pubmed/35139480
http://dx.doi.org/10.1016/j.redox.2022.102242
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author Demircan, Kamil
Chillon, Thilo Samson
Sun, Qian
Heller, Raban Arved
Klingenberg, Georg Jochen
Hirschbil-Bremer, Ines Maria
Seemann, Petra
Diegmann, Joachim
Bachmann, Manuel
Moghaddam, Arash
Schomburg, Lutz
author_facet Demircan, Kamil
Chillon, Thilo Samson
Sun, Qian
Heller, Raban Arved
Klingenberg, Georg Jochen
Hirschbil-Bremer, Ines Maria
Seemann, Petra
Diegmann, Joachim
Bachmann, Manuel
Moghaddam, Arash
Schomburg, Lutz
author_sort Demircan, Kamil
collection PubMed
description The essential trace element selenium (Se) is of central importance for human health and particularly for a regular functioning of the immune system. In the context of the current pandemic, Se deficiency in patients with COVID-19 correlated with disease severity and mortality risk. Selenium has been reported to be associated with the immune response following vaccination, but it is unknown whether this also applies to SARS-CoV-2 vaccines. In this observational study, adult health care workers (n = 126) who received two consecutive anti-SARS-CoV-2 vaccinations by BNT162b2 were followed for up to 24 weeks, with blood samples collected at the first and second dose and at three and 21 weeks after the second dose. Serum SARS-CoV-2 IgG titres, neutralising antibody potency, total Se and selenoprotein P concentrations, and glutathione peroxidase 3 activity were quantified. All three biomarkers of Se status were significantly correlated at all the time points, and participants who reported supplemental Se intake displayed higher Se concentrations. SARS-CoV-2 IgG titres and neutralising potency were highest three weeks after the second dose and decreased towards the last sampling point. The humoral immune response was not related to any of the three Se status biomarkers. Supplemental Se intake had no effect at any time point on the vaccination response as measured by serum SARS-CoV-2 IgG levels or neutralising potency. Overall, no association was found between Se status or supplemental Se intake and humoral immune response to COVID-19 mRNA vaccination.
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spelling pubmed-88105942022-02-03 Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status Demircan, Kamil Chillon, Thilo Samson Sun, Qian Heller, Raban Arved Klingenberg, Georg Jochen Hirschbil-Bremer, Ines Maria Seemann, Petra Diegmann, Joachim Bachmann, Manuel Moghaddam, Arash Schomburg, Lutz Redox Biol Short Communication The essential trace element selenium (Se) is of central importance for human health and particularly for a regular functioning of the immune system. In the context of the current pandemic, Se deficiency in patients with COVID-19 correlated with disease severity and mortality risk. Selenium has been reported to be associated with the immune response following vaccination, but it is unknown whether this also applies to SARS-CoV-2 vaccines. In this observational study, adult health care workers (n = 126) who received two consecutive anti-SARS-CoV-2 vaccinations by BNT162b2 were followed for up to 24 weeks, with blood samples collected at the first and second dose and at three and 21 weeks after the second dose. Serum SARS-CoV-2 IgG titres, neutralising antibody potency, total Se and selenoprotein P concentrations, and glutathione peroxidase 3 activity were quantified. All three biomarkers of Se status were significantly correlated at all the time points, and participants who reported supplemental Se intake displayed higher Se concentrations. SARS-CoV-2 IgG titres and neutralising potency were highest three weeks after the second dose and decreased towards the last sampling point. The humoral immune response was not related to any of the three Se status biomarkers. Supplemental Se intake had no effect at any time point on the vaccination response as measured by serum SARS-CoV-2 IgG levels or neutralising potency. Overall, no association was found between Se status or supplemental Se intake and humoral immune response to COVID-19 mRNA vaccination. Elsevier 2022-02-03 /pmc/articles/PMC8810594/ /pubmed/35139480 http://dx.doi.org/10.1016/j.redox.2022.102242 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Short Communication
Demircan, Kamil
Chillon, Thilo Samson
Sun, Qian
Heller, Raban Arved
Klingenberg, Georg Jochen
Hirschbil-Bremer, Ines Maria
Seemann, Petra
Diegmann, Joachim
Bachmann, Manuel
Moghaddam, Arash
Schomburg, Lutz
Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title_full Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title_fullStr Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title_full_unstemmed Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title_short Humoral immune response to COVID-19 mRNA vaccination in relation to selenium status
title_sort humoral immune response to covid-19 mrna vaccination in relation to selenium status
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810594/
https://www.ncbi.nlm.nih.gov/pubmed/35139480
http://dx.doi.org/10.1016/j.redox.2022.102242
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