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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8070660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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