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Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection
The rapid spread of the vaccine-resistant Omicron variant of SARS-CoV-2 presents a renewed threat to both unvaccinated and fully vaccinated individuals, and accelerated booster vaccination campaigns are underway to mitigate the ongoing wave of Omicron cases. The degree of immunity provided by standa...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016649/ https://www.ncbi.nlm.nih.gov/pubmed/35441177 http://dx.doi.org/10.1101/2022.04.11.22273694 |
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author | Curlin, Marcel E. Bates, Timothy A. Guzman, Gaelen Schoen, Devin McBride, Savannah K. Carpenter, Samuel D. Tafesse, Fikadu G. |
author_facet | Curlin, Marcel E. Bates, Timothy A. Guzman, Gaelen Schoen, Devin McBride, Savannah K. Carpenter, Samuel D. Tafesse, Fikadu G. |
author_sort | Curlin, Marcel E. |
collection | PubMed |
description | The rapid spread of the vaccine-resistant Omicron variant of SARS-CoV-2 presents a renewed threat to both unvaccinated and fully vaccinated individuals, and accelerated booster vaccination campaigns are underway to mitigate the ongoing wave of Omicron cases. The degree of immunity provided by standard vaccine regimens, boosted regimens, and immune responses elicited by the combination of vaccination and natural infection remain incompletely understood. The relative magnitude, quality and durability of serological responses, and the likelihood of neutralizing protection against future SARS-CoV-2 variants following these modes of exposure are unknown but are critical to the future trajectory of the COVID-19 pandemic. In this study of 99 vaccinated adults, we find that compared with responses after two doses of an mRNA regimen, the immune responses three months after a third vaccine dose and one month after breakthrough infection due to prior variants show dramatic increases in magnitude, potency, and breadth, including increased antibody dependent cellular phagocytosis and robust neutralization of the recently circulating Omicron variant. These results suggest that as the number of Omicron cases rise and as global vaccination and booster campaigns continue, an increasing proportion of the world’s population will acquire potent immune responses that may be protective against future SARS-CoV-2 variants. |
format | Online Article Text |
id | pubmed-9016649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-90166492022-04-19 Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection Curlin, Marcel E. Bates, Timothy A. Guzman, Gaelen Schoen, Devin McBride, Savannah K. Carpenter, Samuel D. Tafesse, Fikadu G. medRxiv Article The rapid spread of the vaccine-resistant Omicron variant of SARS-CoV-2 presents a renewed threat to both unvaccinated and fully vaccinated individuals, and accelerated booster vaccination campaigns are underway to mitigate the ongoing wave of Omicron cases. The degree of immunity provided by standard vaccine regimens, boosted regimens, and immune responses elicited by the combination of vaccination and natural infection remain incompletely understood. The relative magnitude, quality and durability of serological responses, and the likelihood of neutralizing protection against future SARS-CoV-2 variants following these modes of exposure are unknown but are critical to the future trajectory of the COVID-19 pandemic. In this study of 99 vaccinated adults, we find that compared with responses after two doses of an mRNA regimen, the immune responses three months after a third vaccine dose and one month after breakthrough infection due to prior variants show dramatic increases in magnitude, potency, and breadth, including increased antibody dependent cellular phagocytosis and robust neutralization of the recently circulating Omicron variant. These results suggest that as the number of Omicron cases rise and as global vaccination and booster campaigns continue, an increasing proportion of the world’s population will acquire potent immune responses that may be protective against future SARS-CoV-2 variants. Cold Spring Harbor Laboratory 2022-04-12 /pmc/articles/PMC9016649/ /pubmed/35441177 http://dx.doi.org/10.1101/2022.04.11.22273694 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Curlin, Marcel E. Bates, Timothy A. Guzman, Gaelen Schoen, Devin McBride, Savannah K. Carpenter, Samuel D. Tafesse, Fikadu G. Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title | Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title_full | Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title_fullStr | Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title_full_unstemmed | Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title_short | Omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
title_sort | omicron neutralizing antibody response following booster vaccination compared with breakthrough infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016649/ https://www.ncbi.nlm.nih.gov/pubmed/35441177 http://dx.doi.org/10.1101/2022.04.11.22273694 |
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