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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2021
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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. |
format | Online Article Text |
id | pubmed-8580836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
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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