Evidence map›Paper›PMID 40911605›Full record

ArticlePLoS medicine2025

Vaccination strategies to achieve outbreak control for MPXV Clade I with a one-time mass campaign in sub-Saharan Africa: A scenario-based modelling study.

Shihui Jin, Toshiaki R Asakura, Hiroaki Murayama, David Niyukuri, Diafuka Saila-Ngita, Jue Tao Lim, Akira Endo, Borame L Dickens

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Article in PLoS medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

8 authors.

Shihui JinSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.ORCID https://orcid.org/0000-0003-0079-7390
Toshiaki R AsakuraDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene & Tropical Medicine, London, United Kingdom.ORCID https://orcid.org/0000-0001-8838-785X
Hiroaki MurayamaSchool of Medicine, International University of Health and Welfare, Narita, Japan.ORCID https://orcid.org/0000-0002-7219-5981
David NiyukuriDoctoral School, University of Burundi, Bujumbura, Burundi.
Diafuka Saila-NgitaDepartment of Basic Sciences, Faculty of Veterinary Medicine, Université de Kinshasa, Kinshasa, DR Congo.ORCID https://orcid.org/0000-0001-6594-8132
Jue Tao LimLee Kong Chian School of Medicine, Nanyang Technological University, Singapore.ORCID https://orcid.org/0000-0002-2245-0331
Akira EndoSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.ORCID https://orcid.org/0000-0001-6377-7296
Borame L DickensSaw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.ORCID https://orcid.org/0000-0003-1592-1745

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLimited mpox vaccination coverage, declining cross-protection from historical smallpox vaccination campaigns, and persistent zoonotic reservoirs leave many sub-Saharan countries susceptible to mpox outbreaks. With millions of vaccine doses made available to the region since late 2024 and the absence of country-specific guidelines for allocation, estimating the country-specific impact of one-time mass vaccination strategies is necessary for ongoing outbreaks and other countries at future risk. METHODS AND

findingsWe adapted a next generation matrix model to project disease transmission potential for 47 sub-Saharan countries from 2025 to 2050 under four transmission scenarios with different contributions of community versus sexual contacts. The model was informed by mpox datasets from Clade Ia and Ib outbreaks in the Democratic Republic of Congo (DRC), and incorporated country-specific demographics, contact patterns, and historical smallpox vaccination coverage. We then assessed strategies to reduce disease transmissibility by calculating country-specific minimum vaccine coverages and evaluating one-time, age-specific mass vaccination campaigns. At least 20 of the 47 countries are estimated to require vaccination in 2025, and 36 in 2050, to guard against potentially forthcoming national outbreaks. For 11 Clade I-affected countries, the minimum required coverage is estimated to range from 0%-4.8% to 14.5%-19.5% in 2025 with increasing sexual transmission, rising to 0%-10.8% and 22.6%-26.0% in 2050, respectively. The prioritised age group for vaccination shifts from 0-4 years to 20-29 years with additional sexual transmission. Note that all the projections were based on the best available evidence of Clade I transmission in the DRC as of December 2024.

interpretationWith diminishing smallpox-vaccination-induced immunity, increasing disease transmissibility and potential for persistent outbreaks are expected for mpox, necessitating growing vaccine demand for outbreak containment. Given probable supply constraints, our findings could guide the ongoing and future mass vaccination efforts in sub-Saharan Africa by emphasising the prioritisation of high-risk groups, where allocation strategies are tailored to the evolving epidemiological landscape of each country.

Indexed as

Disease OutbreaksMass VaccinationMpox, MonkeypoxSmallpox VaccineVaccinia virusAdolescentAdultAfrica South of the SaharaChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedVaccinationSmallpox Vaccine

Identifiers

PMID40911605
PMCPMC12412972

What Socratic holds

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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 Socratic graph.