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Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses
COVID-19 mRNA vaccines protect against severe disease and hospitalization. Neutralizing antibodies (NAbs) are a first-line defense mechanism, but protective NAb responses are variable. Currently, NAb testing is not widely available. This study employed a lateral flow assay for monitoring NAb levels...
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/PMC9504054/ https://www.ncbi.nlm.nih.gov/pubmed/36146537 http://dx.doi.org/10.3390/vaccines10091459 |
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author | Roeder, Alexa J. Koehler, Megan A. Jasbi, Paniz McKechnie, Davis Vanderhoof, John Edwards, Baylee A. Gonzalez-Moa, Maria J. Seit-Nebi, Alim Svarovsky, Sergei A. Lake, Douglas F. |
author_facet | Roeder, Alexa J. Koehler, Megan A. Jasbi, Paniz McKechnie, Davis Vanderhoof, John Edwards, Baylee A. Gonzalez-Moa, Maria J. Seit-Nebi, Alim Svarovsky, Sergei A. Lake, Douglas F. |
author_sort | Roeder, Alexa J. |
collection | PubMed |
description | COVID-19 mRNA vaccines protect against severe disease and hospitalization. Neutralizing antibodies (NAbs) are a first-line defense mechanism, but protective NAb responses are variable. Currently, NAb testing is not widely available. This study employed a lateral flow assay for monitoring NAb levels postvaccination and natural infection, using a finger-stick drop of blood. We report longitudinal NAb data from BNT162b2 (Pfizer) and mRNA-1273 (Moderna) recipients after second and third doses. Results demonstrate a third dose of mRNA vaccine elicits higher and more durable NAb titers than the second dose, independent of manufacturer, sex, and age. Our analyses also revealed that vaccinated individuals could be categorized as strong, moderate, and poorly neutralizing responders. After the second dose, 34% of subjects were classified as strong responders, compared to 79% after the third dose. The final months of this study coincided with the emergence of the SARS-CoV-2 Omicron variant and symptomatic breakthrough infections within our study population. Lastly, we show that NAb levels sufficient for protection from symptomatic infection with early SARS-CoV-2 variants were not protective against Omicron infection and disease. This work highlights the need for accessible vaccine response monitoring for use in healthcare, such that individuals, particularly those in vulnerable populations, can make informed vaccination decisions. |
format | Online Article Text |
id | pubmed-9504054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95040542022-09-24 Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses Roeder, Alexa J. Koehler, Megan A. Jasbi, Paniz McKechnie, Davis Vanderhoof, John Edwards, Baylee A. Gonzalez-Moa, Maria J. Seit-Nebi, Alim Svarovsky, Sergei A. Lake, Douglas F. Vaccines (Basel) Article COVID-19 mRNA vaccines protect against severe disease and hospitalization. Neutralizing antibodies (NAbs) are a first-line defense mechanism, but protective NAb responses are variable. Currently, NAb testing is not widely available. This study employed a lateral flow assay for monitoring NAb levels postvaccination and natural infection, using a finger-stick drop of blood. We report longitudinal NAb data from BNT162b2 (Pfizer) and mRNA-1273 (Moderna) recipients after second and third doses. Results demonstrate a third dose of mRNA vaccine elicits higher and more durable NAb titers than the second dose, independent of manufacturer, sex, and age. Our analyses also revealed that vaccinated individuals could be categorized as strong, moderate, and poorly neutralizing responders. After the second dose, 34% of subjects were classified as strong responders, compared to 79% after the third dose. The final months of this study coincided with the emergence of the SARS-CoV-2 Omicron variant and symptomatic breakthrough infections within our study population. Lastly, we show that NAb levels sufficient for protection from symptomatic infection with early SARS-CoV-2 variants were not protective against Omicron infection and disease. This work highlights the need for accessible vaccine response monitoring for use in healthcare, such that individuals, particularly those in vulnerable populations, can make informed vaccination decisions. MDPI 2022-09-03 /pmc/articles/PMC9504054/ /pubmed/36146537 http://dx.doi.org/10.3390/vaccines10091459 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 Roeder, Alexa J. Koehler, Megan A. Jasbi, Paniz McKechnie, Davis Vanderhoof, John Edwards, Baylee A. Gonzalez-Moa, Maria J. Seit-Nebi, Alim Svarovsky, Sergei A. Lake, Douglas F. Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title | Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title_full | Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title_fullStr | Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title_full_unstemmed | Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title_short | Longitudinal Comparison of Neutralizing Antibody Responses to COVID-19 mRNA Vaccines after Second and Third Doses |
title_sort | longitudinal comparison of neutralizing antibody responses to covid-19 mrna vaccines after second and third doses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9504054/ https://www.ncbi.nlm.nih.gov/pubmed/36146537 http://dx.doi.org/10.3390/vaccines10091459 |
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