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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-8918633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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