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Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein

The emergence of COVID-19 has led to a worldwide challenge for the rapid development of vaccines. Several types of safe and effective vaccines have been available in a time frame never seen before. Now that several hundred million people have been vaccinated there is an opportunity to compare vaccin...

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Autores principales: Romero-Pinedo, Salvador, Quesada, Marina, Horndler, Lydia, Álvarez-Fernández, Stela, Olmo, Asunción, Abia, David, Alarcón, Balbino, Delgado, Pilar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918633/
https://www.ncbi.nlm.nih.gov/pubmed/35296086
http://dx.doi.org/10.3389/fimmu.2022.809285
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author Romero-Pinedo, Salvador
Quesada, Marina
Horndler, Lydia
Álvarez-Fernández, Stela
Olmo, Asunción
Abia, David
Alarcón, Balbino
Delgado, Pilar
author_facet Romero-Pinedo, Salvador
Quesada, Marina
Horndler, Lydia
Álvarez-Fernández, Stela
Olmo, Asunción
Abia, David
Alarcón, Balbino
Delgado, Pilar
author_sort Romero-Pinedo, Salvador
collection PubMed
description The emergence of COVID-19 has led to a worldwide challenge for the rapid development of vaccines. Several types of safe and effective vaccines have been available in a time frame never seen before. Now that several hundred million people have been vaccinated there is an opportunity to compare vaccines in terms of protection and immune response. Here, we have applied a highly sensitive multiplexed flow cytometry method to measure simultaneously IgM, IgG1 and IgA anti-spike protein antibodies generated in response to three vaccines: ChAdOx1 (Oxford-AstraZeneca), mRNA-1273 (Moderna), and BNT162b2 (Pfizer-BioNTech). We have found that mRNA vaccines (mRNA-1273 and BNT162b2) induce a stronger humoral response, both after the first and the second dose, than the adenovirus-based ChAdOx1 vaccine. We also found that, in the elderly, antibody titers negatively correlate with the age of the donor but, also, that antibody titers remain stable for at least 6 months after complete vaccination. Finally, we found that one dose of BNT162b2 is sufficient to induce the highest antibody titers in seropositive pre-vaccination donors. We hope these data will help to guide future decisions on vaccination strategies.
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spelling pubmed-89186332022-03-15 Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein Romero-Pinedo, Salvador Quesada, Marina Horndler, Lydia Álvarez-Fernández, Stela Olmo, Asunción Abia, David Alarcón, Balbino Delgado, Pilar Front Immunol Immunology The emergence of COVID-19 has led to a worldwide challenge for the rapid development of vaccines. Several types of safe and effective vaccines have been available in a time frame never seen before. Now that several hundred million people have been vaccinated there is an opportunity to compare vaccines in terms of protection and immune response. Here, we have applied a highly sensitive multiplexed flow cytometry method to measure simultaneously IgM, IgG1 and IgA anti-spike protein antibodies generated in response to three vaccines: ChAdOx1 (Oxford-AstraZeneca), mRNA-1273 (Moderna), and BNT162b2 (Pfizer-BioNTech). We have found that mRNA vaccines (mRNA-1273 and BNT162b2) induce a stronger humoral response, both after the first and the second dose, than the adenovirus-based ChAdOx1 vaccine. We also found that, in the elderly, antibody titers negatively correlate with the age of the donor but, also, that antibody titers remain stable for at least 6 months after complete vaccination. Finally, we found that one dose of BNT162b2 is sufficient to induce the highest antibody titers in seropositive pre-vaccination donors. We hope these data will help to guide future decisions on vaccination strategies. Frontiers Media S.A. 2022-02-28 /pmc/articles/PMC8918633/ /pubmed/35296086 http://dx.doi.org/10.3389/fimmu.2022.809285 Text en Copyright © 2022 Romero-Pinedo, Quesada, Horndler, Álvarez-Fernández, Olmo, Abia, Alarcón and Delgado https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Romero-Pinedo, Salvador
Quesada, Marina
Horndler, Lydia
Álvarez-Fernández, Stela
Olmo, Asunción
Abia, David
Alarcón, Balbino
Delgado, Pilar
Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title_full Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title_fullStr Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title_full_unstemmed Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title_short Vaccine Type-, Age- and Past Infection-Dependence of the Humoral Response to SARS-CoV-2 Spike S Protein
title_sort vaccine type-, age- and past infection-dependence of the humoral response to sars-cov-2 spike s protein
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918633/
https://www.ncbi.nlm.nih.gov/pubmed/35296086
http://dx.doi.org/10.3389/fimmu.2022.809285
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