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BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity

We examined the impact of pre-existing SARS-CoV-2-specific cellular immunity on BNT162b2 mRNA COVID-19 vaccine reactogenicity. Of 96 healthcare workers (HCWs), 76% reported any vaccine reaction (first dose: 70%, second dose: 67%), none of which was severe. Following first dose, systemic reactions we...

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Autores principales: Vizcarra, Pilar, Haemmerle, Johannes, Velasco, Hector, Velasco, Tamara, Fernández-Escribano, Marina, Vallejo, Alejandro, Casado, José L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580836/
https://www.ncbi.nlm.nih.gov/pubmed/34802792
http://dx.doi.org/10.1016/j.vaccine.2021.10.074
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author Vizcarra, Pilar
Haemmerle, Johannes
Velasco, Hector
Velasco, Tamara
Fernández-Escribano, Marina
Vallejo, Alejandro
Casado, José L.
author_facet Vizcarra, Pilar
Haemmerle, Johannes
Velasco, Hector
Velasco, Tamara
Fernández-Escribano, Marina
Vallejo, Alejandro
Casado, José L.
author_sort Vizcarra, Pilar
collection PubMed
description We examined the impact of pre-existing SARS-CoV-2-specific cellular immunity on BNT162b2 mRNA COVID-19 vaccine reactogenicity. Of 96 healthcare workers (HCWs), 76% reported any vaccine reaction (first dose: 70%, second dose: 67%), none of which was severe. Following first dose, systemic reactions were significantly more frequent among HCWs with past infection than in infection-naïve individuals, and among HCWs with pre-existing cellular immunity than in those without it. The rate of systemic reactions after second dose was 1.7 and 2.0-times higher than after first dose among infection-naïve HCWs and those without pre-existing cellular immunity, respectively. Levels of SARS-CoV-2-specific T-cells before vaccination were higher in HCWs with systemic reactions after the first dose than in those without them. BNT162b2 vaccine reactogenicity after first dose is attributable to pre-existing cellular immunity elicited by prior COVID-19 or cross-reactivity. Reactogenicity following second dose suggests an immunity-boosting effect. Overall, these data may reduce negative attitudes towards COVID-19 vaccines. Study Registration. The study was registered on clinicaltrials.gov, NCT04402827.
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spelling pubmed-85808362021-11-12 BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity Vizcarra, Pilar Haemmerle, Johannes Velasco, Hector Velasco, Tamara Fernández-Escribano, Marina Vallejo, Alejandro Casado, José L. Vaccine Short Communication We examined the impact of pre-existing SARS-CoV-2-specific cellular immunity on BNT162b2 mRNA COVID-19 vaccine reactogenicity. Of 96 healthcare workers (HCWs), 76% reported any vaccine reaction (first dose: 70%, second dose: 67%), none of which was severe. Following first dose, systemic reactions were significantly more frequent among HCWs with past infection than in infection-naïve individuals, and among HCWs with pre-existing cellular immunity than in those without it. The rate of systemic reactions after second dose was 1.7 and 2.0-times higher than after first dose among infection-naïve HCWs and those without pre-existing cellular immunity, respectively. Levels of SARS-CoV-2-specific T-cells before vaccination were higher in HCWs with systemic reactions after the first dose than in those without them. BNT162b2 vaccine reactogenicity after first dose is attributable to pre-existing cellular immunity elicited by prior COVID-19 or cross-reactivity. Reactogenicity following second dose suggests an immunity-boosting effect. Overall, these data may reduce negative attitudes towards COVID-19 vaccines. Study Registration. The study was registered on clinicaltrials.gov, NCT04402827. Elsevier Ltd. 2021-12-17 2021-11-11 /pmc/articles/PMC8580836/ /pubmed/34802792 http://dx.doi.org/10.1016/j.vaccine.2021.10.074 Text en © 2021 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Short Communication
Vizcarra, Pilar
Haemmerle, Johannes
Velasco, Hector
Velasco, Tamara
Fernández-Escribano, Marina
Vallejo, Alejandro
Casado, José L.
BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title_full BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title_fullStr BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title_full_unstemmed BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title_short BNT162b2 mRNA COVID-19 vaccine Reactogenicity: The key role of immunity
title_sort bnt162b2 mrna covid-19 vaccine reactogenicity: the key role of immunity
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8580836/
https://www.ncbi.nlm.nih.gov/pubmed/34802792
http://dx.doi.org/10.1016/j.vaccine.2021.10.074
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