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Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2
BACKGROUND: Breakthrough infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) has occurred in populations with high vaccination rates. METHODS: In a longitudinal cohort study, pre-breakthrough infection sera for Omicron breakthroughs (n = 12) we...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424516/ https://www.ncbi.nlm.nih.gov/pubmed/36088193 http://dx.doi.org/10.1016/j.vaccine.2022.08.058 |
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author | Williams, Erin Colson, Jordan Valiathan, Ranjini Carreño, Juan Manuel Krammer, Florian Hoffer, Michael Pallikkuth, Suresh Pahwa, Savita Andrews, David |
author_facet | Williams, Erin Colson, Jordan Valiathan, Ranjini Carreño, Juan Manuel Krammer, Florian Hoffer, Michael Pallikkuth, Suresh Pahwa, Savita Andrews, David |
author_sort | Williams, Erin |
collection | PubMed |
description | BACKGROUND: Breakthrough infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) has occurred in populations with high vaccination rates. METHODS: In a longitudinal cohort study, pre-breakthrough infection sera for Omicron breakthroughs (n = 12) were analyzed. Assays utilized include a laboratory-developed solid phase binding assay to recombinant spike protein, a commercial assay to the S1 domain of the spike protein calibrated to the World Health Organization (WHO) standard, and a commercial solid-phase surrogate neutralizing activity (SNA) assay. All assays employed spike protein preparations based on sequences from the Wuhan-Hu-1 strain. RESULTS: Pre-breakthrough binding antibody titers ranged from 1:800 to 1:51,200 for the laboratory-developed binding assay, which correlated well and agreed quantitatively with the commercial spike S1 domain WHO calibrated assay. SNA was detected in 10/12 (83%) samples. CONCLUSIONS: Neither high binding titers nor SNA were markers of protection from Omicron infection/re-infection. |
format | Online Article Text |
id | pubmed-9424516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94245162022-08-30 Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 Williams, Erin Colson, Jordan Valiathan, Ranjini Carreño, Juan Manuel Krammer, Florian Hoffer, Michael Pallikkuth, Suresh Pahwa, Savita Andrews, David Vaccine Short Communication BACKGROUND: Breakthrough infection with the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant (B.1.1.529) has occurred in populations with high vaccination rates. METHODS: In a longitudinal cohort study, pre-breakthrough infection sera for Omicron breakthroughs (n = 12) were analyzed. Assays utilized include a laboratory-developed solid phase binding assay to recombinant spike protein, a commercial assay to the S1 domain of the spike protein calibrated to the World Health Organization (WHO) standard, and a commercial solid-phase surrogate neutralizing activity (SNA) assay. All assays employed spike protein preparations based on sequences from the Wuhan-Hu-1 strain. RESULTS: Pre-breakthrough binding antibody titers ranged from 1:800 to 1:51,200 for the laboratory-developed binding assay, which correlated well and agreed quantitatively with the commercial spike S1 domain WHO calibrated assay. SNA was detected in 10/12 (83%) samples. CONCLUSIONS: Neither high binding titers nor SNA were markers of protection from Omicron infection/re-infection. Published by Elsevier Ltd. 2022-09-29 2022-08-30 /pmc/articles/PMC9424516/ /pubmed/36088193 http://dx.doi.org/10.1016/j.vaccine.2022.08.058 Text en © 2022 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Short Communication Williams, Erin Colson, Jordan Valiathan, Ranjini Carreño, Juan Manuel Krammer, Florian Hoffer, Michael Pallikkuth, Suresh Pahwa, Savita Andrews, David Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title | Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title_full | Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title_fullStr | Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title_full_unstemmed | Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title_short | Permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral SARS-CoV-2 |
title_sort | permissive omicron breakthrough infections in individuals with binding or neutralizing antibodies to ancestral sars-cov-2 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424516/ https://www.ncbi.nlm.nih.gov/pubmed/36088193 http://dx.doi.org/10.1016/j.vaccine.2022.08.058 |
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