The effect of time since measles vaccination and age at first dose on measles vaccine effectiveness - A systematic review.


Journal

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

Informations de publication

Date de publication:
16 01 2020
Historique:
received: 03 06 2019
revised: 16 09 2019
accepted: 27 10 2019
pubmed: 17 11 2019
medline: 13 2 2021
entrez: 17 11 2019
Statut: ppublish

Résumé

In settings where measles has been eliminated, vaccine-derived immunity may in theory wane more rapidly due to a lack of immune boosting by circulating measles virus. We aimed to assess whether measles vaccine effectiveness (VE) waned over time, and if so, whether differentially in measles-eliminated and measles-endemic settings. We performed a systematic literature review of studies that reported VE and time since vaccination with measles-containing vaccine (MCV). We extracted information on case definition (clinical symptoms and/or laboratory diagnosis), method of vaccination status ascertainment (medical record or vaccine registry), as well as any biases which may have arisen from cold chain issues and a lack of an age at first dose of MCV. We then used linear regression to evaluate VE as a function of age at first dose of MCV and time since MCV. After screening 14,782 citations, we identified three full-text articles from measles-eliminated settings and 33 articles from measles-endemic settings. In elimination settings, two-dose VE estimates increased as age at first dose of MCV increased and decreased as time since MCV increased; however, the small number of studies available limited interpretation. In measles-endemic settings, one-dose VE increased by 1.5% (95% CI 0.5, 2.5) for every month increase in age at first dose of MCV. We found no evidence of waning VE in endemic settings. The paucity of data from measles-eliminated settings indicates that additional studies and approaches (such as studies using proxies including laboratory correlates of protection) are needed to answer the question of whether VE in measles-eliminated settings wanes. Age at first dose of MCV was the most important factor in determining VE. More VE studies need to be conducted in elimination settings, and standards should be developed for information collected and reported in such studies.

Sections du résumé

BACKGROUND
In settings where measles has been eliminated, vaccine-derived immunity may in theory wane more rapidly due to a lack of immune boosting by circulating measles virus. We aimed to assess whether measles vaccine effectiveness (VE) waned over time, and if so, whether differentially in measles-eliminated and measles-endemic settings.
METHODS
We performed a systematic literature review of studies that reported VE and time since vaccination with measles-containing vaccine (MCV). We extracted information on case definition (clinical symptoms and/or laboratory diagnosis), method of vaccination status ascertainment (medical record or vaccine registry), as well as any biases which may have arisen from cold chain issues and a lack of an age at first dose of MCV. We then used linear regression to evaluate VE as a function of age at first dose of MCV and time since MCV.
RESULTS
After screening 14,782 citations, we identified three full-text articles from measles-eliminated settings and 33 articles from measles-endemic settings. In elimination settings, two-dose VE estimates increased as age at first dose of MCV increased and decreased as time since MCV increased; however, the small number of studies available limited interpretation. In measles-endemic settings, one-dose VE increased by 1.5% (95% CI 0.5, 2.5) for every month increase in age at first dose of MCV. We found no evidence of waning VE in endemic settings.
CONCLUSIONS
The paucity of data from measles-eliminated settings indicates that additional studies and approaches (such as studies using proxies including laboratory correlates of protection) are needed to answer the question of whether VE in measles-eliminated settings wanes. Age at first dose of MCV was the most important factor in determining VE. More VE studies need to be conducted in elimination settings, and standards should be developed for information collected and reported in such studies.

Identifiants

pubmed: 31732326
pii: S0264-410X(19)31479-3
doi: 10.1016/j.vaccine.2019.10.090
pmc: PMC6970218
pii:
doi:

Substances chimiques

Measles Vaccine 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

460-469

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.

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Auteurs

Stephanie L Hughes (SL)

Public Health Ontario, Toronto, Ontario, Canada.

Shelly Bolotin (S)

Public Health Ontario, Toronto, Ontario, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.

Sumaiya Khan (S)

Public Health Ontario, Toronto, Ontario, Canada.

Ye Li (Y)

Public Health Ontario, Toronto, Ontario, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Caitlin Johnson (C)

Public Health Ontario, Toronto, Ontario, Canada.

Lindsay Friedman (L)

Public Health Ontario, Toronto, Ontario, Canada.

Andrea C Tricco (AC)

Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada; Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada.

Susan J M Hahné (SJM)

Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, the Netherlands.

Jane M Heffernan (JM)

Centre for Disease Modelling, Department of Mathematics & Statistics, York University, Toronto, Ontario, Canada.

Alya Dabbagh (A)

Department of Immunisation, Vaccines, and Biologicals, World Health Organization, Geneva, Switzerland.

David N Durrheim (DN)

Hunter New England Health, New Lambton Heights, New South Wales, Australia; School of Medicine and Public Health, University of Newcastle, New South Wales, Australia; Public Health and Tropical Medicine, James Cook University, Queensland, Australia.

Walter A Orenstein (WA)

Emory University School of Medicine, Emory University, Atlanta, GA, United States; Emory Vaccine Center, Emory University, Atlanta, GA, United States.

William J Moss (WJ)

International Vaccine Access Center, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, United States.

Mark Jit (M)

Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom; Modelling and Economics Unit, Public Health England, London, United Kingdom.

Natasha S Crowcroft (NS)

Public Health Ontario, Toronto, Ontario, Canada; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; ICES, Toronto, Ontario, Canada. Electronic address: natasha.crowcroft@utoronto.ca.

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