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Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines
Around the world, rollout of COVID-19 vaccines has been used as a strategy to end COVID-19-related restrictions and the pandemic. Several COVID-19 vaccine platforms have successfully protected against severe SARS-CoV-2 infection and subsequent deaths. Here, we compared humoral and cellular immunity...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782527/ https://www.ncbi.nlm.nih.gov/pubmed/36560562 http://dx.doi.org/10.3390/vaccines10122152 |
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author | Samanovic, Marie I. Oom, Aaron L. Cornelius, Amber R. Gray-Gaillard, Sophie L. Karmacharya, Trishala Tuen, Michael Wilson, Jimmy P. Tasissa, Meron F. Goins, Shelby Herati, Ramin Sedaghat Mulligan, Mark J. |
author_facet | Samanovic, Marie I. Oom, Aaron L. Cornelius, Amber R. Gray-Gaillard, Sophie L. Karmacharya, Trishala Tuen, Michael Wilson, Jimmy P. Tasissa, Meron F. Goins, Shelby Herati, Ramin Sedaghat Mulligan, Mark J. |
author_sort | Samanovic, Marie I. |
collection | PubMed |
description | Around the world, rollout of COVID-19 vaccines has been used as a strategy to end COVID-19-related restrictions and the pandemic. Several COVID-19 vaccine platforms have successfully protected against severe SARS-CoV-2 infection and subsequent deaths. Here, we compared humoral and cellular immunity in response to either infection or vaccination. We examined SARS-CoV-2 spike-specific immune responses from Pfizer/BioNTech BNT162b2, Moderna mRNA-1273, Janssen Ad26.COV2.S, and SARS-CoV-2 infection approximately 4 months post-exposure or vaccination. We found that these three vaccines all generate relatively similar immune responses and elicit a stronger response than natural infection. However, antibody responses to recent viral variants are diminished across all groups. The similarity of immune responses from the three vaccines studied here is an important finding in maximizing global protection as vaccination campaigns continue. |
format | Online Article Text |
id | pubmed-9782527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97825272022-12-24 Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines Samanovic, Marie I. Oom, Aaron L. Cornelius, Amber R. Gray-Gaillard, Sophie L. Karmacharya, Trishala Tuen, Michael Wilson, Jimmy P. Tasissa, Meron F. Goins, Shelby Herati, Ramin Sedaghat Mulligan, Mark J. Vaccines (Basel) Article Around the world, rollout of COVID-19 vaccines has been used as a strategy to end COVID-19-related restrictions and the pandemic. Several COVID-19 vaccine platforms have successfully protected against severe SARS-CoV-2 infection and subsequent deaths. Here, we compared humoral and cellular immunity in response to either infection or vaccination. We examined SARS-CoV-2 spike-specific immune responses from Pfizer/BioNTech BNT162b2, Moderna mRNA-1273, Janssen Ad26.COV2.S, and SARS-CoV-2 infection approximately 4 months post-exposure or vaccination. We found that these three vaccines all generate relatively similar immune responses and elicit a stronger response than natural infection. However, antibody responses to recent viral variants are diminished across all groups. The similarity of immune responses from the three vaccines studied here is an important finding in maximizing global protection as vaccination campaigns continue. MDPI 2022-12-15 /pmc/articles/PMC9782527/ /pubmed/36560562 http://dx.doi.org/10.3390/vaccines10122152 Text en © 2022 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 Samanovic, Marie I. Oom, Aaron L. Cornelius, Amber R. Gray-Gaillard, Sophie L. Karmacharya, Trishala Tuen, Michael Wilson, Jimmy P. Tasissa, Meron F. Goins, Shelby Herati, Ramin Sedaghat Mulligan, Mark J. Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title | Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title_full | Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title_fullStr | Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title_full_unstemmed | Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title_short | Vaccine-Acquired SARS-CoV-2 Immunity versus Infection-Acquired Immunity: A Comparison of Three COVID-19 Vaccines |
title_sort | vaccine-acquired sars-cov-2 immunity versus infection-acquired immunity: a comparison of three covid-19 vaccines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782527/ https://www.ncbi.nlm.nih.gov/pubmed/36560562 http://dx.doi.org/10.3390/vaccines10122152 |
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