Evidence map›Paper›PMID 41827013›Full record

ArticleMalaria journal2026

Timing of the fourth dose of RTS,S/AS01 malaria vaccine in perennial settings: a modelling study.

Daniella Figueroa-Downing, Sherrie L Kelly, Aurélien Cavelan, Melissa A Penny, Josephine Malinga

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Article in Malaria journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daniella Figueroa-DowningSwiss Tropical and Public Health Institute, Allschwil, Switzerland.
Sherrie L KellySwiss Tropical and Public Health Institute, Allschwil, Switzerland.
Aurélien CavelanUniversity of Basel, Basel, Switzerland.
Melissa A PennyThe Kids Research Institute Australia, Nedlands, WA, Australia. melissa.penny@uwa.edu.au.
Josephine MalingaThe Kids Research Institute Australia, Nedlands, WA, Australia.

Funding

Gates Foundation INV-025569Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung SNF Professorship PP00P3_203450
6 · The paper itself

Abstract

backgroundThe recommendation of the RTS,S/AS01 malaria vaccine for use in children in moderate to high transmission areas by the WHO in 2021 provided another crucial tool in reducing malaria morbidity and mortality. As countries introduce the RTS,S/AS01 vaccine, there is an interest in exploring vaccination schedules that align with existing routine health touchpoints and to optimize vaccine coverage.

methodsThis study used OpenMalaria, an individual-based, stochastic model of malaria transmission and disease progression, to assess the impact of different vaccination timing schedules and coverage on uncomplicated malaria cases, severe malaria cases, and malaria-related deaths across different archetypal transmission settings. We ran simulations comparing fourth dose protection against infection and timings at 6-, 9-, 12-, 15- and 18-month intervals following the primary series, including exploring ranges of plausible protection assumptions for many of the dose timings.

resultsThe primary series substantially reduces the malaria burden across transmission settings, regardless of timing of the fourth vaccine dose. For example, at a baseline Plasmodium falciparum prevalence in 2-10 year olds (PfPR

conclusionsA fourth dose delivered between 15- and 21-months of age (corresponding to a 6-12 month interval after the third dose) with high population coverage will likely avert the largest proportion of cases of uncomplicated malaria, severe malaria, and deaths in perennial settings, across transmission intensities. Therefore, the delivery of the fourth dose of the RTS,S/AS01 vaccine can be tailored to country-specific context and linked to existing health touchpoints to ensure adequate coverage of this dose to optimize its impact.

Indexed as

Immunization ScheduleMalaria, FalciparumMalaria VaccinesChildChild, PreschoolHumansInfantVaccines, SyntheticMalaria VaccinesRTS,S-AS01 vaccineVaccines, SyntheticMalariaMalaria vaccineMathematical modellingRTS,S/AS01Vaccine impact

Identifiers

PMID41827013
PMCPMC13097953

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.