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.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2023
Historique:
received: 08 03 2023
accepted: 01 09 2023
medline: 22 9 2023
pubmed: 20 9 2023
entrez: 20 9 2023
Statut: epublish

Résumé

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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 37729332
doi: 10.1371/journal.pone.0291678
pii: PONE-D-23-06056
pmc: PMC10511074
doi:

Substances chimiques

BNT162 Vaccine 0
COVID-19 Vaccines 0
Vaccines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0291678

Informations de copyright

Copyright: 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 public domain dedication.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Maya R Sternberg (MR)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Amelia Johnson (A)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Justice King (J)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Akilah R Ali (AR)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Lauren Linde (L)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Abiola O Awofeso (AO)

Community Health Administration, DC Department of Health, Washington, District of Columbia, United States of America.

Jodee S Baker (JS)

Division of Population Health, Utah Department of Health and Human Services, Salt Lake City, Utah, United States of America.

Nagla S Bayoumi (NS)

Communicable Disease Service, New Jersey Department of Health, Trenton, New Jersey, United States of America.

Steven Broadway (S)

Division of Disease Control and Health Protection, Florida Department of Health, Tallahassee, Florida, United States of America.

Katherine Busen (K)

Division of Communicable Disease, Michigan Department of Health and Human Services, Lansing, Michigan, United States of America.

Carolyn Chang (C)

Communicable Disease Service, New York City Department of Health and Mental Hygiene, Long Island City, New York, United States of America.

Iris Cheng (I)

Bureau of Immunization, New York City Department of Health and Mental Hygiene, Long Island City, New York, United States of America.

Mike Cima (M)

Epidemilogy, Arkansas Department of Health, Little Rock, Arkansas, United States of America.

Abi Collingwood (A)

Division of Population Health, Utah Department of Health and Human Services, Salt Lake City, Utah, United States of America.

Vajeera Dorabawila (V)

Bureau of Surveillance and Data Systems, Division of Epidemiology, Albany, New York State Department of Health, New York, NY, United States of America.

Cherie Drenzek (C)

Acute Epidemiology, Georgia Department of Public Health, Atlanta, Georgia, United States of America.

Aaron Fleischauer (A)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Ashley Gent (A)

Division of Disease Control and Health Protection, Florida Department of Health, Tallahassee, Florida, United States of America.

Amanda Hartley (A)

Communicable and Environmental Diseases and Emergency Preparedness, Nashville, Tennessee Department of Health, Nashville, Tennessee, United States of America.

Liam Hicks (L)

Bureau of Infectious Disease and Services, Arizona Department of Health Services, Phoenix, Arizona, United States of America.

Mikhail Hoskins (M)

Communicable Disease, North Carolina Department of Health and Human Services, Raleigh, North Carolina, United States of America.

Amanda Jara (A)

Acute Epidemiology, Georgia Department of Public Health, Atlanta, Georgia, United States of America.

Amanda Jones (A)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Saadiah I Khan (SI)

Communicable Disease Service, New Jersey Department of Health, Trenton, New Jersey, United States of America.

Ishrat Kamal-Ahmed (I)

Division of Public Health, Nebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.

Sarah Kangas (S)

COVID-19 Data and Surveillance Unit, Wisconsin Department of Health Services, Madison, Wisconsin, United States of America.

Fnu Kanishka (F)

Division of Public Health, Nebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.

Alison Kleppinger (A)

Epidemiology and Infectious Disease Section, Connecticut Department of Public Health, Hartford, Connecticut, United States of America.

Anna Kocharian (A)

COVID-19 Data and Surveillance Unit, Wisconsin Department of Health Services, Madison, Wisconsin, United States of America.

Tomás M León (TM)

Center for Infectious Diseases, California Department of Public Health, Sacramento, California, United States of America.

Ruth Link-Gelles (R)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

B Casey Lyons (BC)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

John Masarik (J)

Community Health Administration, DC Department of Health, Washington, District of Columbia, United States of America.

Andrea May (A)

Bureau of Epidemiology and Public Health Informatics, Kansas Department of Health and Environment, Kansas, Missouri, United States of America.

Donald McCormick (D)

Epidemilogy, Arkansas Department of Health, Little Rock, Arkansas, United States of America.

Stephanie Meyer (S)

Infectious Disease Epidemiology, Prevention and Control Division, Minnesota Department of Health, Saint Paul, Minnesota, United States of America.

Lauren Milroy (L)

Disease Epidemiology and Prevention Division, Indiana Department of Health, Indianapolis, Indiana, United States of America.

Keeley J Morris (KJ)

Infectious Disease Epidemiology, Prevention and Control Division, Minnesota Department of Health, Saint Paul, Minnesota, United States of America.

Lauren Nelson (L)

Center for Infectious Diseases, California Department of Public Health, Sacramento, California, United States of America.

Enaholo Omoike (E)

Division of Communicable Disease, Michigan Department of Health and Human Services, Lansing, Michigan, United States of America.

Komal Patel (K)

Acute Epidemiology, Georgia Department of Public Health, Atlanta, Georgia, United States of America.

Michael Pietrowski (M)

Division of Disease Control, Philadelphia Department of Public Health, Philadelphia, Pennsylvania, United States of America.

Melissa A Pike (MA)

Disease Control and Public Health Response Division, Colorado Department of Public Health and Environment, Denver, Colorado, United States of America.

Tamara Pilishvili (T)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Xandy Peterson Pompa (X)

Bureau of Infectious Disease and Services, Arizona Department of Health Services, Phoenix, Arizona, United States of America.

Charles Powell (C)

Epidemiology and Infectious Disease Section, Connecticut Department of Public Health, Hartford, Connecticut, United States of America.

Kevin Praetorius (K)

CDC Foundation, Atlanta, Georgia, United States of America.

Eli Rosenberg (E)

Bureau of Surveillance and Data Systems, Division of Epidemiology, Albany, New York State Department of Health, New York, NY, United States of America.

Adam Schiller (A)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Mayra L Smith-Coronado (ML)

Disease Control and Public Health Response Division, Colorado Department of Public Health and Environment, Denver, Colorado, United States of America.

Emma Stanislawski (E)

Epidemiology and Response Division, New Mexico Department of Health, Santa Fe, New Mexico, United States of America.

Kyle Strand (K)

Division of Public Health, Nebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.

Buddhi P Tilakaratne (BP)

Community Health Administration, DC Department of Health, Washington, District of Columbia, United States of America.

Hailey Vest (H)

Disease Epidemiology and Prevention Division, Indiana Department of Health, Indianapolis, Indiana, United States of America.

Caleb Wiedeman (C)

Communicable and Environmental Diseases and Emergency Preparedness, Nashville, Tennessee Department of Health, Nashville, Tennessee, United States of America.

Allison Zaldivar (A)

Bureau of Epidemiology and Public Health Informatics, Kansas Department of Health and Environment, Kansas, Missouri, United States of America.

Benjamin Silk (B)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

Heather M Scobie (HM)

COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.

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