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Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis

mRNA-based SARS-CoV-2 vaccines offer a preventive strategy against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infections that is of interest in the care of patients on hemodialysis (HDP). We measured humoral immune responses in 72 HDP after standard vaccination with two doses of th...

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Autores principales: Jahn, Michael, Korth, Johannes, Dorsch, Oliver, Anastasiou, Olympia Evdoxia, Sorge-Hädicke, Burkhard, Tyczynski, Bartosz, Gäckler, Anja, Witzke, Oliver, Dittmer, Ulf, Dolff, Sebastian, Wilde, Benjamin, Kribben, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070660/
https://www.ncbi.nlm.nih.gov/pubmed/33918085
http://dx.doi.org/10.3390/vaccines9040360
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author Jahn, Michael
Korth, Johannes
Dorsch, Oliver
Anastasiou, Olympia Evdoxia
Sorge-Hädicke, Burkhard
Tyczynski, Bartosz
Gäckler, Anja
Witzke, Oliver
Dittmer, Ulf
Dolff, Sebastian
Wilde, Benjamin
Kribben, Andreas
author_facet Jahn, Michael
Korth, Johannes
Dorsch, Oliver
Anastasiou, Olympia Evdoxia
Sorge-Hädicke, Burkhard
Tyczynski, Bartosz
Gäckler, Anja
Witzke, Oliver
Dittmer, Ulf
Dolff, Sebastian
Wilde, Benjamin
Kribben, Andreas
author_sort Jahn, Michael
collection PubMed
description mRNA-based SARS-CoV-2 vaccines offer a preventive strategy against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infections that is of interest in the care of patients on hemodialysis (HDP). We measured humoral immune responses in 72 HDP after standard vaccination with two doses of the mRNA-based SARS-CoV-2 vaccine BNT162b2 (Pfizer-BioNTech). Antibody responses were evaluated with an anti-SARS-CoV-2 IgG ChemiLuminescent ImmunoAssay (CLIA) two weeks after the second dose. In addition, SARS-CoV-2 IgG was determined in a control of 16 healthy healthcare workers (HCW). The control group of HCW has shown a strong antibody response with a median (MD (Q1; Q3)) antibody titer of 800.0 AU/mL (520.5; 800.0). In comparison to HCW, HDP under 60 years of age responded equally (597.0 AU/mL (410.5; 800.0), p = 0.051). However, the antibody responses of the HDP negatively correlated with age (r(2) = 0.2954 p < 0.0001), leading to significantly lower antibody titers in HDP over 60 years (280.0 AU/mL (45.7; 477.0), p < 0.0001). To thoroughly understand the immunogenicity of the new mRNA-based vaccines in HDP, longitudinal data on the effectiveness and durability of antibody responses are needed. Modifications of immunization schedules should be considered in HDP with low or without antibody responsiveness after standard vaccination to boost immune reactivity and prolong protective effects in these vulnerable patients.
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spelling pubmed-80706602021-04-26 Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis Jahn, Michael Korth, Johannes Dorsch, Oliver Anastasiou, Olympia Evdoxia Sorge-Hädicke, Burkhard Tyczynski, Bartosz Gäckler, Anja Witzke, Oliver Dittmer, Ulf Dolff, Sebastian Wilde, Benjamin Kribben, Andreas Vaccines (Basel) Communication mRNA-based SARS-CoV-2 vaccines offer a preventive strategy against severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infections that is of interest in the care of patients on hemodialysis (HDP). We measured humoral immune responses in 72 HDP after standard vaccination with two doses of the mRNA-based SARS-CoV-2 vaccine BNT162b2 (Pfizer-BioNTech). Antibody responses were evaluated with an anti-SARS-CoV-2 IgG ChemiLuminescent ImmunoAssay (CLIA) two weeks after the second dose. In addition, SARS-CoV-2 IgG was determined in a control of 16 healthy healthcare workers (HCW). The control group of HCW has shown a strong antibody response with a median (MD (Q1; Q3)) antibody titer of 800.0 AU/mL (520.5; 800.0). In comparison to HCW, HDP under 60 years of age responded equally (597.0 AU/mL (410.5; 800.0), p = 0.051). However, the antibody responses of the HDP negatively correlated with age (r(2) = 0.2954 p < 0.0001), leading to significantly lower antibody titers in HDP over 60 years (280.0 AU/mL (45.7; 477.0), p < 0.0001). To thoroughly understand the immunogenicity of the new mRNA-based vaccines in HDP, longitudinal data on the effectiveness and durability of antibody responses are needed. Modifications of immunization schedules should be considered in HDP with low or without antibody responsiveness after standard vaccination to boost immune reactivity and prolong protective effects in these vulnerable patients. MDPI 2021-04-08 /pmc/articles/PMC8070660/ /pubmed/33918085 http://dx.doi.org/10.3390/vaccines9040360 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Jahn, Michael
Korth, Johannes
Dorsch, Oliver
Anastasiou, Olympia Evdoxia
Sorge-Hädicke, Burkhard
Tyczynski, Bartosz
Gäckler, Anja
Witzke, Oliver
Dittmer, Ulf
Dolff, Sebastian
Wilde, Benjamin
Kribben, Andreas
Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title_full Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title_fullStr Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title_full_unstemmed Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title_short Humoral Response to SARS-CoV-2-Vaccination with BNT162b2 (Pfizer-BioNTech) in Patients on Hemodialysis
title_sort humoral response to sars-cov-2-vaccination with bnt162b2 (pfizer-biontech) in patients on hemodialysis
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070660/
https://www.ncbi.nlm.nih.gov/pubmed/33918085
http://dx.doi.org/10.3390/vaccines9040360
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