Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Curlin, Marcel E., Bates, Timothy A., Guzman, Gaelen, Schoen, Devin, McBride, Savannah K., Carpenter, Samuel D., Tafesse, Fikadu G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2022
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
_version_ 1784688571996700672
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
work_keys_str_mv AT curlinmarcele omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT batestimothya omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT guzmangaelen omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT schoendevin omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT mcbridesavannahk omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT carpentersamueld omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection
AT tafessefikadug omicronneutralizingantibodyresponsefollowingboostervaccinationcomparedwithbreakthroughinfection