Is neglect of self-clearance biasing TB vaccine impact estimates?


Journal

BMJ global health
ISSN: 2059-7908
Titre abrégé: BMJ Glob Health
Pays: England
ID NLM: 101685275

Informations de publication

Date de publication:
08 2023
Historique:
received: 11 05 2023
accepted: 13 07 2023
medline: 11 8 2023
pubmed: 10 8 2023
entrez: 9 8 2023
Statut: ppublish

Résumé

Mathematical modelling has been used extensively to estimate the potential impact of new tuberculosis vaccines, with the majority of existing models assuming that individuals with For both countries, we calibrated a tuberculosis model to a scenario without self-clearance and to various scenarios with self-clearance. To account for the current uncertainty in self-clearance properties, we varied the rate of self-clearance, and the level of protection against reinfection in self-cleared individuals. We introduced potential new vaccines in 2025, exploring vaccines that work in uninfected or infected individuals only, or that are effective regardless of infection status, and modelling scenarios with different levels of vaccine efficacy in self-cleared individuals. We then estimated the relative disease incidence reduction in 2050 for each vaccine compared with the no vaccination scenario. The inclusion of self-clearance increased the estimated relative reductions in incidence in 2050 for vaccines effective only in uninfected individuals, by a maximum of 12% in China and 8% in India. The inclusion of self-clearance increased the estimated impact of vaccines only effective in infected individuals in some scenarios and decreased it in others, by a maximum of 14% in China and 15% in India. As would be expected, the inclusion of self-clearance had minimal impact on estimated reductions in incidence for vaccines that work regardless of infection status. Our work suggests that the neglect of self-clearance in mathematical models of tuberculosis vaccines does not result in substantially biased estimates of tuberculosis vaccine impact. It may, however, mean that we are slightly underestimating the relative advantages of vaccines that work in uninfected individuals only compared with those that work in infected individuals.

Sections du résumé

BACKGROUND
Mathematical modelling has been used extensively to estimate the potential impact of new tuberculosis vaccines, with the majority of existing models assuming that individuals with
METHODS
For both countries, we calibrated a tuberculosis model to a scenario without self-clearance and to various scenarios with self-clearance. To account for the current uncertainty in self-clearance properties, we varied the rate of self-clearance, and the level of protection against reinfection in self-cleared individuals. We introduced potential new vaccines in 2025, exploring vaccines that work in uninfected or infected individuals only, or that are effective regardless of infection status, and modelling scenarios with different levels of vaccine efficacy in self-cleared individuals. We then estimated the relative disease incidence reduction in 2050 for each vaccine compared with the no vaccination scenario.
FINDINGS
The inclusion of self-clearance increased the estimated relative reductions in incidence in 2050 for vaccines effective only in uninfected individuals, by a maximum of 12% in China and 8% in India. The inclusion of self-clearance increased the estimated impact of vaccines only effective in infected individuals in some scenarios and decreased it in others, by a maximum of 14% in China and 15% in India. As would be expected, the inclusion of self-clearance had minimal impact on estimated reductions in incidence for vaccines that work regardless of infection status.
INTERPRETATIONS
Our work suggests that the neglect of self-clearance in mathematical models of tuberculosis vaccines does not result in substantially biased estimates of tuberculosis vaccine impact. It may, however, mean that we are slightly underestimating the relative advantages of vaccines that work in uninfected individuals only compared with those that work in infected individuals.

Identifiants

pubmed: 37558271
pii: bmjgh-2023-012799
doi: 10.1136/bmjgh-2023-012799
pmc: PMC10414120
pii:
doi:

Substances chimiques

Tuberculosis Vaccines 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Bill & Melinda Gates Foundation
ID : INV-001754
Pays : United States
Organisme : Bill & Melinda Gates Foundation
ID : INV-035506
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI147321
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Danny Scarponi (D)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK danny.scarponi@lshtm.ac.uk.

Rebecca A Clark (RA)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Chathika Krishan Weerasuriya (CK)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Jon Emery (J)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Rein M G J Houben (RMGJ)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Richard White (R)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

Nicky McCreesh (N)

Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.

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Classifications MeSH