Population-Weighted Seroprevalence From Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection, Vaccination, and Hybrid Immunity Among US Blood Donations From January to December 2021.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
03 10 2022
Historique:
received: 03 04 2022
pubmed: 11 6 2022
medline: 6 10 2022
entrez: 10 6 2022
Statut: ppublish

Résumé

Previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19) vaccination, independently and combined ("hybrid immunity"), result in partial protection from subsequent infection and strong protection from severe disease. Proportions of the US population who have been infected, vaccinated, or have hybrid immunity remain unclear, posing a challenge for assessing effective pandemic mitigation strategies. In this serial cross-sectional study, nationwide blood donor specimens collected during January-December 2021 were tested for anti-spike and anti-nucleocapsid antibodies, and donor COVID-19 vaccination history of ≥1 dose was collected. Monthly seroprevalence induced from SARS-CoV-2 infection, COVID-19 vaccination, or both, were estimated. Estimates were weighted to account for demographic differences from the general population and were compared temporally and by demographic factors. Overall, 1 123 855 blood samples were assayed. From January to December 2021, the weighted percentage of donations with seropositivity changed as follows: seropositivity due to vaccination without previous infection, increase from 3.5% (95% confidence interval, 3.4%-3.7%) to 64.0%, (63.5%-64.5%); seropositivity due to previous infection without vaccination, decrease from 15.6% (15.2%-16.0%) to 11.7% (11.4%-12.0%); and seropositivity due to hybrid immunity, increase from 0.7% (0.6%-0.7%) to 18.9% (18.5%-19.3%). Combined seroprevalence from infection, vaccination, or both increased from 19.8% (19.3%-20.2%) to 94.5% (93.5%-94.0%). Infection- and vaccination-induced antibody responses varied significantly by age, race-ethnicity, and region, but not by sex. Our results indicate substantial increases in population humoral immunity from SARS-CoV-2 infection, COVID-19 vaccination, and hybrid immunity during 2021. These findings are important to consider in future COVID-19 studies and long-term pandemic mitigation efforts.

Sections du résumé

BACKGROUND
Previous severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and coronavirus disease 2019 (COVID-19) vaccination, independently and combined ("hybrid immunity"), result in partial protection from subsequent infection and strong protection from severe disease. Proportions of the US population who have been infected, vaccinated, or have hybrid immunity remain unclear, posing a challenge for assessing effective pandemic mitigation strategies.
METHODS
In this serial cross-sectional study, nationwide blood donor specimens collected during January-December 2021 were tested for anti-spike and anti-nucleocapsid antibodies, and donor COVID-19 vaccination history of ≥1 dose was collected. Monthly seroprevalence induced from SARS-CoV-2 infection, COVID-19 vaccination, or both, were estimated. Estimates were weighted to account for demographic differences from the general population and were compared temporally and by demographic factors.
RESULTS
Overall, 1 123 855 blood samples were assayed. From January to December 2021, the weighted percentage of donations with seropositivity changed as follows: seropositivity due to vaccination without previous infection, increase from 3.5% (95% confidence interval, 3.4%-3.7%) to 64.0%, (63.5%-64.5%); seropositivity due to previous infection without vaccination, decrease from 15.6% (15.2%-16.0%) to 11.7% (11.4%-12.0%); and seropositivity due to hybrid immunity, increase from 0.7% (0.6%-0.7%) to 18.9% (18.5%-19.3%). Combined seroprevalence from infection, vaccination, or both increased from 19.8% (19.3%-20.2%) to 94.5% (93.5%-94.0%). Infection- and vaccination-induced antibody responses varied significantly by age, race-ethnicity, and region, but not by sex.
CONCLUSIONS
Our results indicate substantial increases in population humoral immunity from SARS-CoV-2 infection, COVID-19 vaccination, and hybrid immunity during 2021. These findings are important to consider in future COVID-19 studies and long-term pandemic mitigation efforts.

Identifiants

pubmed: 35684973
pii: 6605072
doi: 10.1093/cid/ciac470
pmc: PMC9214177
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

S254-S263

Subventions

Organisme : CDC HHS
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interest. M. P. B. reports being an employee of Vitalant Research Institute and receiving grant funding for their institution from Ortho Clinical Diagnostics. E. G. reports research funding to their employer Vitalant Research Institute from Ortho Clinical Diagnostics. They also report the provision of reagents for other studies from Ortho Clinical Diagnostics and Roche. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Michael P Busch (MP)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Susan L Stramer (SL)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

Mars Stone (M)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Elaine A Yu (EA)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Eduard Grebe (E)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Edward Notari (E)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

Paula Saa (P)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

Robyn Ferg (R)

Westat, Rockville, Maryland, USA.

Irene Molina Manrique (IM)

Westat, Rockville, Maryland, USA.

Natalia Weil (N)

Westat, Rockville, Maryland, USA.

Rebecca V Fink (RV)

Westat, Rockville, Maryland, USA.

Matthew E Levy (ME)

Westat, Rockville, Maryland, USA.

Valerie Green (V)

Creative Testing Solutions, Tempe, Arizona, USA.

Sherri Cyrus (S)

Creative Testing Solutions, Tempe, Arizona, USA.

Phillip C Williamson (PC)

Creative Testing Solutions, Tempe, Arizona, USA.

James Haynes (J)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

Jamel Groves (J)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

David Krysztof (D)

American Red Cross, Scientific Affairs, Gaithersburg and Rockville, Maryland, USA.

Brian Custer (B)

Vitalant Research Institute, San Francisco, California, USA.
Department of Laboratory Medicine, University of California San Francisco, San Francisco, California, USA.

Steve Kleinman (S)

Vitalant Research Institute, San Francisco, California, USA.

Brad J Biggerstaff (BJ)

Centers for Disease Control and Prevention, Fort Collins, Colorado, USA.

Jean D Opsomer (JD)

Westat, Rockville, Maryland, USA.

Jefferson M Jones (JM)

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

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