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Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada

BACKGROUND: The evolving proportion of the population considered immunologically naive versus primed for more efficient immune memory response to SARS-CoV-2 has implications for risk assessment. We sought to chronicle vaccine- and infection-induced seroprevalence across the first 7 waves of the COVI...

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Autores principales: Skowronski, Danuta M., Kaweski, Samantha E., Irvine, Michael A., Kim, Shinhye, Chuang, Erica S.Y., Sabaiduc, Suzana, Fraser, Mieke, Reyes, Romina C., Henry, Bonnie, Levett, Paul N., Petric, Martin, Krajden, Mel, Sekirov, Inna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Impact Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828974/
https://www.ncbi.nlm.nih.gov/pubmed/36507788
http://dx.doi.org/10.1503/cmaj.221335
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author Skowronski, Danuta M.
Kaweski, Samantha E.
Irvine, Michael A.
Kim, Shinhye
Chuang, Erica S.Y.
Sabaiduc, Suzana
Fraser, Mieke
Reyes, Romina C.
Henry, Bonnie
Levett, Paul N.
Petric, Martin
Krajden, Mel
Sekirov, Inna
author_facet Skowronski, Danuta M.
Kaweski, Samantha E.
Irvine, Michael A.
Kim, Shinhye
Chuang, Erica S.Y.
Sabaiduc, Suzana
Fraser, Mieke
Reyes, Romina C.
Henry, Bonnie
Levett, Paul N.
Petric, Martin
Krajden, Mel
Sekirov, Inna
author_sort Skowronski, Danuta M.
collection PubMed
description BACKGROUND: The evolving proportion of the population considered immunologically naive versus primed for more efficient immune memory response to SARS-CoV-2 has implications for risk assessment. We sought to chronicle vaccine- and infection-induced seroprevalence across the first 7 waves of the COVID-19 pandemic in British Columbia, Canada. METHODS: During 8 cross-sectional serosurveys conducted between March 2020 and August 2022, we obtained anonymized residual sera from children and adults who attended an outpatient laboratory network in the Lower Mainland (Greater Vancouver and Fraser Valley). We used at least 3 immunoassays per serosurvey to detect SARS-CoV-2 spike and nucleocapsid antibodies. We assessed any seroprevalence (vaccineor infection-induced, or both), defined by positivity on any 2 assays, and infection-induced seroprevalence, also defined by dual-assay positivity but requiring both antinucleocapsid and antispike detection. We used estimates of infection-induced seroprevalence to explore underascertainment of infections by surveillance case reports. RESULTS: By January 2021, we estimated that any seroprevalence remained less than 5%, increasing with vaccine rollout to 56% by May–June 2021, 83% by September–October 2021 and 95% by March 2022. Infection-induced seroprevalence remained less than 15% through September–October 2021, increasing across Omicron waves to 42% by March 2022 and 61% by July–August 2022. By August 2022, 70%–80% of children younger than 20 years and 60%–70% of adults aged 20–59 years had been infected, but fewer than half of adults aged 60 years and older had been infected. Compared with estimates of infection-induced seroprevalence, surveillance case reports underestimated infections 12-fold between September 2021 and March 2022 and 92-fold between March 2022 and August 2022. INTERPRETATION: By August 2022, most children and adults younger than 60 years had evidence of both SARS-CoV-2 vaccination and infection. As previous evidence suggests that a history of both exposures may induce stronger, more durable hybrid immunity than either exposure alone, older adults — who have the lowest infection rates but highest risk of severe outcomes — continue to warrant prioritized vaccination.
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spelling pubmed-98289742023-01-13 Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada Skowronski, Danuta M. Kaweski, Samantha E. Irvine, Michael A. Kim, Shinhye Chuang, Erica S.Y. Sabaiduc, Suzana Fraser, Mieke Reyes, Romina C. Henry, Bonnie Levett, Paul N. Petric, Martin Krajden, Mel Sekirov, Inna CMAJ Research BACKGROUND: The evolving proportion of the population considered immunologically naive versus primed for more efficient immune memory response to SARS-CoV-2 has implications for risk assessment. We sought to chronicle vaccine- and infection-induced seroprevalence across the first 7 waves of the COVID-19 pandemic in British Columbia, Canada. METHODS: During 8 cross-sectional serosurveys conducted between March 2020 and August 2022, we obtained anonymized residual sera from children and adults who attended an outpatient laboratory network in the Lower Mainland (Greater Vancouver and Fraser Valley). We used at least 3 immunoassays per serosurvey to detect SARS-CoV-2 spike and nucleocapsid antibodies. We assessed any seroprevalence (vaccineor infection-induced, or both), defined by positivity on any 2 assays, and infection-induced seroprevalence, also defined by dual-assay positivity but requiring both antinucleocapsid and antispike detection. We used estimates of infection-induced seroprevalence to explore underascertainment of infections by surveillance case reports. RESULTS: By January 2021, we estimated that any seroprevalence remained less than 5%, increasing with vaccine rollout to 56% by May–June 2021, 83% by September–October 2021 and 95% by March 2022. Infection-induced seroprevalence remained less than 15% through September–October 2021, increasing across Omicron waves to 42% by March 2022 and 61% by July–August 2022. By August 2022, 70%–80% of children younger than 20 years and 60%–70% of adults aged 20–59 years had been infected, but fewer than half of adults aged 60 years and older had been infected. Compared with estimates of infection-induced seroprevalence, surveillance case reports underestimated infections 12-fold between September 2021 and March 2022 and 92-fold between March 2022 and August 2022. INTERPRETATION: By August 2022, most children and adults younger than 60 years had evidence of both SARS-CoV-2 vaccination and infection. As previous evidence suggests that a history of both exposures may induce stronger, more durable hybrid immunity than either exposure alone, older adults — who have the lowest infection rates but highest risk of severe outcomes — continue to warrant prioritized vaccination. CMA Impact Inc. 2022-12-05 2022-12-05 /pmc/articles/PMC9828974/ /pubmed/36507788 http://dx.doi.org/10.1503/cmaj.221335 Text en © 2022 CMA Impact Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research
Skowronski, Danuta M.
Kaweski, Samantha E.
Irvine, Michael A.
Kim, Shinhye
Chuang, Erica S.Y.
Sabaiduc, Suzana
Fraser, Mieke
Reyes, Romina C.
Henry, Bonnie
Levett, Paul N.
Petric, Martin
Krajden, Mel
Sekirov, Inna
Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title_full Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title_fullStr Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title_full_unstemmed Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title_short Serial cross-sectional estimation of vaccine-and infection-induced SARS-CoV-2 seroprevalence in British Columbia, Canada
title_sort serial cross-sectional estimation of vaccine-and infection-induced sars-cov-2 seroprevalence in british columbia, canada
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9828974/
https://www.ncbi.nlm.nih.gov/pubmed/36507788
http://dx.doi.org/10.1503/cmaj.221335
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