Comparative performance of between-population vaccine allocation strategies with applications for emerging pandemics.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
10 03 2023
Historique:
received: 17 08 2022
revised: 19 12 2022
accepted: 20 12 2022
pubmed: 26 1 2023
medline: 7 3 2023
entrez: 25 1 2023
Statut: ppublish

Résumé

Vaccine allocation decisions during emerging pandemics have proven to be challenging due to competing ethical, practical, and political considerations. Complicating decision making, policy makers need to consider vaccine allocation strategies that balance needs both within and between populations. When vaccine stockpiles are limited, doses should be allocated in locations to maximize their impact. Using a susceptible-exposed-infectious-recovered (SEIR) model we examine optimal vaccine allocation decisions across two populations considering the impact of characteristics of the population (e.g., size, underlying immunity, heterogeneous risk structure, interaction), vaccine (e.g., vaccine efficacy), pathogen (e.g., transmissibility), and delivery (e.g., varying speed and timing of rollout). Across a wide range of characteristics considered, we find that vaccine allocation proportional to population size (i.e., pro-rata allocation) performs either better or comparably to nonproportional allocation strategies in minimizing the cumulative number of infections. These results may argue in favor of sharing of vaccines between locations in the context of an epidemic caused by an emerging pathogen, where many epidemiologic characteristics may not be known.

Identifiants

pubmed: 36697312
pii: S0264-410X(22)01579-1
doi: 10.1016/j.vaccine.2022.12.053
pmc: PMC10075509
mid: NIHMS1869722
pii:
doi:

Substances chimiques

Vaccines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1864-1874

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007535
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA261277
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Eva Rumpler, Lee Kennedy-Shaffer, and Rafia Bosan have no conflicts of interest to disclose. Keya Joshi reports a paid internship unrelated to COVID-19 with Janssen Pharmaceuticals. Marc Lipsitch reports grants from CDC, NIH, UK NIHR, and Pfizer, personal fees from Merck, Janssen, Sanofi Pasteur, Bristol Myers Squibb, and Peter Diamandis/Abundance Platinum, outside the submitted work; and Unpaid advice to One Day Sooner, Pfizer, Janssen, Astra-Zeneca, COVAX (United Biomedical).

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Auteurs

Keya Joshi (K)

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard TH Chan School of Public Health, 02115 Boston, MA, USA.

Eva Rumpler (E)

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard TH Chan School of Public Health, 02115 Boston, MA, USA.

Lee Kennedy-Shaffer (L)

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard TH Chan School of Public Health, 02115 Boston, MA, USA; Department of Mathematics & Statistics, Vassar College, 12604 Poughkeepsie, NY, USA.

Rafia Bosan (R)

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard TH Chan School of Public Health, 02115 Boston, MA, USA.

Marc Lipsitch (M)

Center for Communicable Disease Dynamics, Department of Epidemiology, Harvard TH Chan School of Public Health, 02115 Boston, MA, USA.

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Classifications MeSH