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Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period
BACKGROUND: SARS-CoV-2 Omicron variants have the potential to impact vaccine effectiveness and duration of vaccine-derived immunity. We analyzed U.S. multi-jurisdictional COVID-19 vaccine breakthrough surveillance data to examine potential waning of protection against SARS-CoV-2 infection for the Pf...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511074/ https://www.ncbi.nlm.nih.gov/pubmed/37729332 http://dx.doi.org/10.1371/journal.pone.0291678 |
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author | Sternberg, Maya R. Johnson, Amelia King, Justice Ali, Akilah R. Linde, Lauren Awofeso, Abiola O. Baker, Jodee S. Bayoumi, Nagla S. Broadway, Steven Busen, Katherine Chang, Carolyn Cheng, Iris Cima, Mike Collingwood, Abi Dorabawila, Vajeera Drenzek, Cherie Fleischauer, Aaron Gent, Ashley Hartley, Amanda Hicks, Liam Hoskins, Mikhail Jara, Amanda Jones, Amanda Khan, Saadiah I. Kamal-Ahmed, Ishrat Kangas, Sarah Kanishka, FNU Kleppinger, Alison Kocharian, Anna León, Tomás M. Link-Gelles, Ruth Lyons, B. Casey Masarik, John May, Andrea McCormick, Donald Meyer, Stephanie Milroy, Lauren Morris, Keeley J. Nelson, Lauren Omoike, Enaholo Patel, Komal Pietrowski, Michael Pike, Melissa A. Pilishvili, Tamara Peterson Pompa, Xandy Powell, Charles Praetorius, Kevin Rosenberg, Eli Schiller, Adam Smith-Coronado, Mayra L. Stanislawski, Emma Strand, Kyle Tilakaratne, Buddhi P. Vest, Hailey Wiedeman, Caleb Zaldivar, Allison Silk, Benjamin Scobie, Heather M. |
author_facet | Sternberg, Maya R. Johnson, Amelia King, Justice Ali, Akilah R. Linde, Lauren Awofeso, Abiola O. Baker, Jodee S. Bayoumi, Nagla S. Broadway, Steven Busen, Katherine Chang, Carolyn Cheng, Iris Cima, Mike Collingwood, Abi Dorabawila, Vajeera Drenzek, Cherie Fleischauer, Aaron Gent, Ashley Hartley, Amanda Hicks, Liam Hoskins, Mikhail Jara, Amanda Jones, Amanda Khan, Saadiah I. Kamal-Ahmed, Ishrat Kangas, Sarah Kanishka, FNU Kleppinger, Alison Kocharian, Anna León, Tomás M. Link-Gelles, Ruth Lyons, B. Casey Masarik, John May, Andrea McCormick, Donald Meyer, Stephanie Milroy, Lauren Morris, Keeley J. Nelson, Lauren Omoike, Enaholo Patel, Komal Pietrowski, Michael Pike, Melissa A. Pilishvili, Tamara Peterson Pompa, Xandy Powell, Charles Praetorius, Kevin Rosenberg, Eli Schiller, Adam Smith-Coronado, Mayra L. Stanislawski, Emma Strand, Kyle Tilakaratne, Buddhi P. Vest, Hailey Wiedeman, Caleb Zaldivar, Allison Silk, Benjamin Scobie, Heather M. |
author_sort | Sternberg, Maya R. |
collection | PubMed |
description | BACKGROUND: SARS-CoV-2 Omicron variants have the potential to impact vaccine effectiveness and duration of vaccine-derived immunity. We analyzed U.S. multi-jurisdictional COVID-19 vaccine breakthrough surveillance data to examine potential waning of protection against SARS-CoV-2 infection for the Pfizer-BioNTech (BNT162b) primary vaccination series by age. METHODS: Weekly numbers of SARS-CoV-2 infections during January 16, 2022–May 28, 2022 were analyzed by age group from 22 U.S. jurisdictions that routinely linked COVID-19 case surveillance and immunization data. A life table approach incorporating line-listed and aggregated COVID-19 case datasets with vaccine administration and U.S. Census data was used to estimate hazard rates of SARS-CoV-2 infections, hazard rate ratios (HRR) and percent reductions in hazard rate comparing unvaccinated people to people vaccinated with a Pfizer-BioNTech primary series only, by age group and time since vaccination. RESULTS: The percent reduction in hazard rates for persons 2 weeks after vaccination with a Pfizer-BioNTech primary series compared with unvaccinated persons was lowest among children aged 5–11 years at 35.5% (95% CI: 33.3%, 37.6%) compared to the older age groups, which ranged from 68.7%–89.6%. By 19 weeks after vaccination, all age groups showed decreases in the percent reduction in the hazard rates compared with unvaccinated people; with the largest declines observed among those aged 5–11 and 12–17 years and more modest declines observed among those 18 years and older. CONCLUSIONS: The decline in vaccine protection against SARS-CoV-2 infection observed in this study is consistent with other studies and demonstrates that national case surveillance data were useful for assessing early signals in age-specific waning of vaccine protection during the initial period of SARS-CoV-2 Omicron variant predominance. The potential for waning immunity during the Omicron period emphasizes the importance of continued monitoring and consideration of optimal timing and provision of booster doses in the future. |
format | Online Article Text |
id | pubmed-10511074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-105110742023-09-21 Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period Sternberg, Maya R. Johnson, Amelia King, Justice Ali, Akilah R. Linde, Lauren Awofeso, Abiola O. Baker, Jodee S. Bayoumi, Nagla S. Broadway, Steven Busen, Katherine Chang, Carolyn Cheng, Iris Cima, Mike Collingwood, Abi Dorabawila, Vajeera Drenzek, Cherie Fleischauer, Aaron Gent, Ashley Hartley, Amanda Hicks, Liam Hoskins, Mikhail Jara, Amanda Jones, Amanda Khan, Saadiah I. Kamal-Ahmed, Ishrat Kangas, Sarah Kanishka, FNU Kleppinger, Alison Kocharian, Anna León, Tomás M. Link-Gelles, Ruth Lyons, B. Casey Masarik, John May, Andrea McCormick, Donald Meyer, Stephanie Milroy, Lauren Morris, Keeley J. Nelson, Lauren Omoike, Enaholo Patel, Komal Pietrowski, Michael Pike, Melissa A. Pilishvili, Tamara Peterson Pompa, Xandy Powell, Charles Praetorius, Kevin Rosenberg, Eli Schiller, Adam Smith-Coronado, Mayra L. Stanislawski, Emma Strand, Kyle Tilakaratne, Buddhi P. Vest, Hailey Wiedeman, Caleb Zaldivar, Allison Silk, Benjamin Scobie, Heather M. PLoS One Research Article BACKGROUND: SARS-CoV-2 Omicron variants have the potential to impact vaccine effectiveness and duration of vaccine-derived immunity. We analyzed U.S. multi-jurisdictional COVID-19 vaccine breakthrough surveillance data to examine potential waning of protection against SARS-CoV-2 infection for the Pfizer-BioNTech (BNT162b) primary vaccination series by age. METHODS: Weekly numbers of SARS-CoV-2 infections during January 16, 2022–May 28, 2022 were analyzed by age group from 22 U.S. jurisdictions that routinely linked COVID-19 case surveillance and immunization data. A life table approach incorporating line-listed and aggregated COVID-19 case datasets with vaccine administration and U.S. Census data was used to estimate hazard rates of SARS-CoV-2 infections, hazard rate ratios (HRR) and percent reductions in hazard rate comparing unvaccinated people to people vaccinated with a Pfizer-BioNTech primary series only, by age group and time since vaccination. RESULTS: The percent reduction in hazard rates for persons 2 weeks after vaccination with a Pfizer-BioNTech primary series compared with unvaccinated persons was lowest among children aged 5–11 years at 35.5% (95% CI: 33.3%, 37.6%) compared to the older age groups, which ranged from 68.7%–89.6%. By 19 weeks after vaccination, all age groups showed decreases in the percent reduction in the hazard rates compared with unvaccinated people; with the largest declines observed among those aged 5–11 and 12–17 years and more modest declines observed among those 18 years and older. CONCLUSIONS: The decline in vaccine protection against SARS-CoV-2 infection observed in this study is consistent with other studies and demonstrates that national case surveillance data were useful for assessing early signals in age-specific waning of vaccine protection during the initial period of SARS-CoV-2 Omicron variant predominance. The potential for waning immunity during the Omicron period emphasizes the importance of continued monitoring and consideration of optimal timing and provision of booster doses in the future. Public Library of Science 2023-09-20 /pmc/articles/PMC10511074/ /pubmed/37729332 http://dx.doi.org/10.1371/journal.pone.0291678 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Sternberg, Maya R. Johnson, Amelia King, Justice Ali, Akilah R. Linde, Lauren Awofeso, Abiola O. Baker, Jodee S. Bayoumi, Nagla S. Broadway, Steven Busen, Katherine Chang, Carolyn Cheng, Iris Cima, Mike Collingwood, Abi Dorabawila, Vajeera Drenzek, Cherie Fleischauer, Aaron Gent, Ashley Hartley, Amanda Hicks, Liam Hoskins, Mikhail Jara, Amanda Jones, Amanda Khan, Saadiah I. Kamal-Ahmed, Ishrat Kangas, Sarah Kanishka, FNU Kleppinger, Alison Kocharian, Anna León, Tomás M. Link-Gelles, Ruth Lyons, B. Casey Masarik, John May, Andrea McCormick, Donald Meyer, Stephanie Milroy, Lauren Morris, Keeley J. Nelson, Lauren Omoike, Enaholo Patel, Komal Pietrowski, Michael Pike, Melissa A. Pilishvili, Tamara Peterson Pompa, Xandy Powell, Charles Praetorius, Kevin Rosenberg, Eli Schiller, Adam Smith-Coronado, Mayra L. Stanislawski, Emma Strand, Kyle Tilakaratne, Buddhi P. Vest, Hailey Wiedeman, Caleb Zaldivar, Allison Silk, Benjamin Scobie, Heather M. Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title | Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title_full | Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title_fullStr | Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title_full_unstemmed | Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title_short | Application of a life table approach to assess duration of BNT162b2 vaccine-derived immunity by age using COVID-19 case surveillance data during the Omicron variant period |
title_sort | application of a life table approach to assess duration of bnt162b2 vaccine-derived immunity by age using covid-19 case surveillance data during the omicron variant period |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511074/ https://www.ncbi.nlm.nih.gov/pubmed/37729332 http://dx.doi.org/10.1371/journal.pone.0291678 |
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