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Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses
The SARS-CoV-2 Delta variant is currently responsible for most infections worldwide, including among fully vaccinated individuals. Although these latter infections are associated with milder COVID-19 disease relative to unvaccinated subjects, the specificity and durability of antibody responses elic...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687475/ https://www.ncbi.nlm.nih.gov/pubmed/34931192 http://dx.doi.org/10.1101/2021.12.08.471707 |
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author | Walls, Alexandra C. Sprouse, Kaitlin R. Joshi, Anshu Bowen, John E. Franko, Nicholas Navarro, Mary Jane Stewart, Cameron McCallum, Matthew Goecker, Erin A. Degli-Angeli, Emily J. Logue, Jenni Greninger, Alex Chu, Helen Veesler, David |
author_facet | Walls, Alexandra C. Sprouse, Kaitlin R. Joshi, Anshu Bowen, John E. Franko, Nicholas Navarro, Mary Jane Stewart, Cameron McCallum, Matthew Goecker, Erin A. Degli-Angeli, Emily J. Logue, Jenni Greninger, Alex Chu, Helen Veesler, David |
author_sort | Walls, Alexandra C. |
collection | PubMed |
description | The SARS-CoV-2 Delta variant is currently responsible for most infections worldwide, including among fully vaccinated individuals. Although these latter infections are associated with milder COVID-19 disease relative to unvaccinated subjects, the specificity and durability of antibody responses elicited by Delta breakthrough cases remain unknown. Here, we demonstrate that breakthrough infections induce serum binding and neutralizing antibody responses that are markedly more potent, durable and resilient to spike mutations observed in variants of concern than those observed in subjects who were infected only or received only two doses of COVID-19 vaccine. However, wee show that Delta breakthrough cases, subjects who were vaccinated after SARS-CoV-2 infection and individuals vaccinated three times (without infection) have serum neutralizing activity of comparable magnitude and breadth indicate that multiple types of exposure or increased number of exposures to SARS-CoV-2 antigen(s) enhance spike-specific antibody responses. Neutralization of the genetically divergent SARS-CoV, however, was moderate with all four cohorts examined, except after four exposures to the SARS-CoV-2 spike, underscoring the importance of developing vaccines eliciting broad sarbecovirus immunity for pandemic preparedness. |
format | Online Article Text |
id | pubmed-8687475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-86874752021-12-21 Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses Walls, Alexandra C. Sprouse, Kaitlin R. Joshi, Anshu Bowen, John E. Franko, Nicholas Navarro, Mary Jane Stewart, Cameron McCallum, Matthew Goecker, Erin A. Degli-Angeli, Emily J. Logue, Jenni Greninger, Alex Chu, Helen Veesler, David bioRxiv Article The SARS-CoV-2 Delta variant is currently responsible for most infections worldwide, including among fully vaccinated individuals. Although these latter infections are associated with milder COVID-19 disease relative to unvaccinated subjects, the specificity and durability of antibody responses elicited by Delta breakthrough cases remain unknown. Here, we demonstrate that breakthrough infections induce serum binding and neutralizing antibody responses that are markedly more potent, durable and resilient to spike mutations observed in variants of concern than those observed in subjects who were infected only or received only two doses of COVID-19 vaccine. However, wee show that Delta breakthrough cases, subjects who were vaccinated after SARS-CoV-2 infection and individuals vaccinated three times (without infection) have serum neutralizing activity of comparable magnitude and breadth indicate that multiple types of exposure or increased number of exposures to SARS-CoV-2 antigen(s) enhance spike-specific antibody responses. Neutralization of the genetically divergent SARS-CoV, however, was moderate with all four cohorts examined, except after four exposures to the SARS-CoV-2 spike, underscoring the importance of developing vaccines eliciting broad sarbecovirus immunity for pandemic preparedness. Cold Spring Harbor Laboratory 2021-12-13 /pmc/articles/PMC8687475/ /pubmed/34931192 http://dx.doi.org/10.1101/2021.12.08.471707 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 Walls, Alexandra C. Sprouse, Kaitlin R. Joshi, Anshu Bowen, John E. Franko, Nicholas Navarro, Mary Jane Stewart, Cameron McCallum, Matthew Goecker, Erin A. Degli-Angeli, Emily J. Logue, Jenni Greninger, Alex Chu, Helen Veesler, David Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title | Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title_full | Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title_fullStr | Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title_full_unstemmed | Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title_short | Delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
title_sort | delta breakthrough infections elicit potent, broad and durable neutralizing antibody responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687475/ https://www.ncbi.nlm.nih.gov/pubmed/34931192 http://dx.doi.org/10.1101/2021.12.08.471707 |
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