Evidence map›Paper›PMID 41882671›Full record

ArticleBMC medicine2026

Public health impact of catch-up vaccination or additional booster doses with pre-erythrocytic malaria vaccine R21/Matrix-M: a modelling study.

Kelly McCain, Hillary M Topazian, Joseph D Challenger, Lucy Okell, Peter Winskill, Azra C Ghani

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Kelly McCainMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK. k.mccain22@imperial.ac.uk.
Hillary M TopazianMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Joseph D ChallengerMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Lucy OkellMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Peter WinskillMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Azra C GhaniMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.

Funding

Medical Research Council MR/X020258/1Open Philanthropy Project GV673604959
6 · The paper itself

Abstract

backgroundThe malaria vaccine R21/Matrix-M is recommended for young children in malaria-endemic regions. However, the small vaccine-eligible population and waning vaccine efficacy mean that routine vaccination is unlikely to prevent severe cases in older children who experience significant malaria burden. As R21/Matrix-M vaccination expands, targeting older age groups may be warranted, depending on funding.

methodsUsing a stochastic, individual-based Plasmodium falciparum malaria transmission model, we estimate the impact of (1) one-off catch-up campaigns with R21/Matrix-M to previously unvaccinated age groups between age 6 months and 14 years, and/or (2) extra boosters at 2, 5, and/or 10 years after the primary series in low, moderate, and high transmission settings. We assume that vaccine immunogenicity in older children is equivalent to that of the standard target age group, though clinical trials have shown lower immunogenicity in older children.

resultsCatch-up campaigns in moderate-to-high transmission settings targeting younger children averted the most uncomplicated cases per 1000 additional doses (358 (95% credible interval (CI) 113-570) in children aged 6 months-2 years at 45% PfPR

conclusionsCatch-up campaigns or extra booster doses of R21/Matrix-M can provide benefits beyond routine administration, with the per-additional-dose value approaching that of routine vaccination, but this varies by transmission and seasonality setting. Further empirical studies, particularly on vaccine efficacy in older children, are warranted to inform policy guidance for malaria vaccination implementation.

Indexed as

Immunization, SecondaryMalaria, FalciparumMalaria VaccinesPublic HealthVaccinationAdolescentChildChild, PreschoolHumansInfantMaleVaccine EfficacyMalaria VaccinesCatch-up vaccinationMalaria controlMalaria transmission modelMalaria vaccineScenario modellingSchool-aged children

Identifiers

PMID41882671
PMCPMC13137673

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.