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Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2

It is not clear whether there is an association between adverse reactions and immune response after vaccination. Seven hundred and thirty-five vaccinees from our University Medical Center vaccination clinic provided information about sex, age and adverse reactions after first and second vaccination...

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Autores principales: Bauernfeind, Stilla, Salzberger, Bernd, Hitzenbichler, Florian, Scigala, Karolina, Einhauser, Sebastian, Wagner, Ralf, Gessner, André, Koestler, Josef, Peterhoff, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538767/
https://www.ncbi.nlm.nih.gov/pubmed/34696197
http://dx.doi.org/10.3390/vaccines9101089
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author Bauernfeind, Stilla
Salzberger, Bernd
Hitzenbichler, Florian
Scigala, Karolina
Einhauser, Sebastian
Wagner, Ralf
Gessner, André
Koestler, Josef
Peterhoff, David
author_facet Bauernfeind, Stilla
Salzberger, Bernd
Hitzenbichler, Florian
Scigala, Karolina
Einhauser, Sebastian
Wagner, Ralf
Gessner, André
Koestler, Josef
Peterhoff, David
author_sort Bauernfeind, Stilla
collection PubMed
description It is not clear whether there is an association between adverse reactions and immune response after vaccination. Seven hundred and thirty-five vaccinees from our University Medical Center vaccination clinic provided information about sex, age and adverse reactions after first and second vaccination with BNT162b2. Adverse reactions were categorized into three groups: no or minor on the injection side, moderate (not further classified) and severe—defined as any symptom(s) resulting in sick leave. We chose 38 vaccinees with the most severe adverse reactions and compared their humoral and T-cell-mediated immune responses after second vaccination with those of 38 sex and age matched controls without or only minor injection-side related adverse reactions. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) anti-receptor binding domain (RBD) IgG titers were detectable in all participants (median 5528; range 958–26,285). Men with severe adverse reactions had 1.5-fold higher median SARS-CoV-2 RBD IgG titers compared to men without adverse reactions (median 7406 versus 4793; p < 0.001). Similarly; neutralization activity was significantly higher in men with severe adverse reactions (half maximal inhibitory concentrations (IC(50)) median 769 versus 485; p < 0.001). Reactogenicity did not influence humoral immune response in women nor T-cell-mediated immune response in any sex. To conclude; adverse reactions after vaccination with BNT162b2 do influence humoral immune response yet only in men and are not a prerequisite for a robust antibody response.
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spelling pubmed-85387672021-10-24 Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2 Bauernfeind, Stilla Salzberger, Bernd Hitzenbichler, Florian Scigala, Karolina Einhauser, Sebastian Wagner, Ralf Gessner, André Koestler, Josef Peterhoff, David Vaccines (Basel) Article It is not clear whether there is an association between adverse reactions and immune response after vaccination. Seven hundred and thirty-five vaccinees from our University Medical Center vaccination clinic provided information about sex, age and adverse reactions after first and second vaccination with BNT162b2. Adverse reactions were categorized into three groups: no or minor on the injection side, moderate (not further classified) and severe—defined as any symptom(s) resulting in sick leave. We chose 38 vaccinees with the most severe adverse reactions and compared their humoral and T-cell-mediated immune responses after second vaccination with those of 38 sex and age matched controls without or only minor injection-side related adverse reactions. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) anti-receptor binding domain (RBD) IgG titers were detectable in all participants (median 5528; range 958–26,285). Men with severe adverse reactions had 1.5-fold higher median SARS-CoV-2 RBD IgG titers compared to men without adverse reactions (median 7406 versus 4793; p < 0.001). Similarly; neutralization activity was significantly higher in men with severe adverse reactions (half maximal inhibitory concentrations (IC(50)) median 769 versus 485; p < 0.001). Reactogenicity did not influence humoral immune response in women nor T-cell-mediated immune response in any sex. To conclude; adverse reactions after vaccination with BNT162b2 do influence humoral immune response yet only in men and are not a prerequisite for a robust antibody response. MDPI 2021-09-27 /pmc/articles/PMC8538767/ /pubmed/34696197 http://dx.doi.org/10.3390/vaccines9101089 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 Article
Bauernfeind, Stilla
Salzberger, Bernd
Hitzenbichler, Florian
Scigala, Karolina
Einhauser, Sebastian
Wagner, Ralf
Gessner, André
Koestler, Josef
Peterhoff, David
Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title_full Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title_fullStr Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title_full_unstemmed Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title_short Association between Reactogenicity and Immunogenicity after Vaccination with BNT162b2
title_sort association between reactogenicity and immunogenicity after vaccination with bnt162b2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8538767/
https://www.ncbi.nlm.nih.gov/pubmed/34696197
http://dx.doi.org/10.3390/vaccines9101089
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