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Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations

OBJECTIVE: To investigate whether SARS-CoV-2 omicron breakthrough infection in individuals after three doses of wildtype-based BNT162b2 increases antibody levels measured by a commercially available wildtype-based immunoassay. METHODS: 16 of 21 individuals in a BNT162b2 vaccination cohort (recruited...

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Autores principales: Perkmann, Thomas, Springer, David N., Mucher, Patrick, Wolzt, Michael, Weseslindtner, Lukas, Haslacher, Helmuth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299948/
https://www.ncbi.nlm.nih.gov/pubmed/37398629
http://dx.doi.org/10.1016/j.jcvp.2023.100157
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author Perkmann, Thomas
Springer, David N.
Mucher, Patrick
Wolzt, Michael
Weseslindtner, Lukas
Haslacher, Helmuth
author_facet Perkmann, Thomas
Springer, David N.
Mucher, Patrick
Wolzt, Michael
Weseslindtner, Lukas
Haslacher, Helmuth
author_sort Perkmann, Thomas
collection PubMed
description OBJECTIVE: To investigate whether SARS-CoV-2 omicron breakthrough infection in individuals after three doses of wildtype-based BNT162b2 increases antibody levels measured by a commercially available wildtype-based immunoassay. METHODS: 16 of 21 individuals in a BNT162b2 vaccination cohort (recruited 129 [129–135] days after dose 3) experienced a breakthrough infection (BTI) between March and September 2022. Antibodies to the receptor binding domain (RBP) of the spike protein (Anti-S) were quantified using the wildtype-based Elecsys SARS-CoV-2 S assay (Roche). Antibody responses of triple vaccinated BTI cases were compared to triple vaccinated individuals without breakthrough infection and to 16 matched individuals after primary omicron infection. RESULTS: In the 16 individuals with primary Omicron infection, the anti-S assay returned only very low results (2.25 [0.61–5.80] U/mL). However, in individuals with BTI, Anti-S levels rose from 7,135 [5,870–17,470] U/mL to 21,705 (7,750–46,137.5) U/mL. At the same time, Anti-S concentrations decreased from 9,120 [7,480–13,480] U/mL to 3,830 (2,390–4,220) U/mL in those 5 of 21 vaccinated only. CONCLUSIONS: Our data suggest that breakthrough infection with omicron can efficiently boost wild-type antibodies in individuals vaccinated with wild-type BNT162b2.
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spelling pubmed-102999482023-06-28 Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations Perkmann, Thomas Springer, David N. Mucher, Patrick Wolzt, Michael Weseslindtner, Lukas Haslacher, Helmuth J Clin Virol Plus Article OBJECTIVE: To investigate whether SARS-CoV-2 omicron breakthrough infection in individuals after three doses of wildtype-based BNT162b2 increases antibody levels measured by a commercially available wildtype-based immunoassay. METHODS: 16 of 21 individuals in a BNT162b2 vaccination cohort (recruited 129 [129–135] days after dose 3) experienced a breakthrough infection (BTI) between March and September 2022. Antibodies to the receptor binding domain (RBP) of the spike protein (Anti-S) were quantified using the wildtype-based Elecsys SARS-CoV-2 S assay (Roche). Antibody responses of triple vaccinated BTI cases were compared to triple vaccinated individuals without breakthrough infection and to 16 matched individuals after primary omicron infection. RESULTS: In the 16 individuals with primary Omicron infection, the anti-S assay returned only very low results (2.25 [0.61–5.80] U/mL). However, in individuals with BTI, Anti-S levels rose from 7,135 [5,870–17,470] U/mL to 21,705 (7,750–46,137.5) U/mL. At the same time, Anti-S concentrations decreased from 9,120 [7,480–13,480] U/mL to 3,830 (2,390–4,220) U/mL in those 5 of 21 vaccinated only. CONCLUSIONS: Our data suggest that breakthrough infection with omicron can efficiently boost wild-type antibodies in individuals vaccinated with wild-type BNT162b2. Published by Elsevier Ltd. 2023-08 2023-06-28 /pmc/articles/PMC10299948/ /pubmed/37398629 http://dx.doi.org/10.1016/j.jcvp.2023.100157 Text en © 2023 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 Article
Perkmann, Thomas
Springer, David N.
Mucher, Patrick
Wolzt, Michael
Weseslindtner, Lukas
Haslacher, Helmuth
Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title_full Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title_fullStr Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title_full_unstemmed Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title_short Breakthrough infections with SARS-CoV-2 omicron efficiently boost antibodies from previous BNT162b2 vaccinations
title_sort breakthrough infections with sars-cov-2 omicron efficiently boost antibodies from previous bnt162b2 vaccinations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299948/
https://www.ncbi.nlm.nih.gov/pubmed/37398629
http://dx.doi.org/10.1016/j.jcvp.2023.100157
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