Evidence map›Paper›PMID 39811540›Full record

ArticleThe Lancet regional health. Southeast Asia2025

Unveiling immunity gaps and determining a suitable age for a third dose of the measles-containing vaccine: a strategic approach to accelerating measles elimination.

Somya Mehra, Sajikapon Kludkleeb, Chutikarn Chaimayo, Pornsawan Leaungwutiwong, Saranath Lawpoolsri, Wirichada Pan-Ngum, Kulkanya Chokephaibulkit, Thundon Ngamprasertchai

Abstract read
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Article in The Lancet regional health. Southeast Asia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Somya MehraMahidol Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.
Sajikapon KludkleebDepartment of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Chutikarn ChaimayoDepartment of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pornsawan LeaungwutiwongDepartment of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Saranath LawpoolsriDepartment of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Wirichada Pan-NgumMahidol Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.
Kulkanya ChokephaibulkitDepartment of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Thundon NgamprasertchaiDepartment of Tropical Hygiene, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: In highly measles immunized countries, immunity gaps in adolescents and young adults are a key issue posing an obstacle to measles elimination. This study aims to identify the gaps by estimating the age-stratified probability of seropositivity, and to ascertain a suitable age for the administration of a third dose of a measles-containing vaccine (MCV3) to effectively fill these gaps. Methods: We retrospectively obtained measles serological results from hospital setting among among individuals aged 13-39 years and developed a serocatalytic dynamic probability model, stratifying seropositivity due to vaccination or natural infection. We calibrated the model to age-stratified seropositivity data within a Bayesian setting using the Metropolis-Hastings algorithm. A scenario analysis to determine a suitable age for MCV3 administration was also performed. Findings: The overall prevalence of measles seropositivity was 65.6% (95% confidence interval [CI]: 61.5-69.6). Posterior predictive curves for the age-stratified seroprevalence exhibited a decreasing trend from ages 13-20 years but an upward trend from 26 to 30 years. The age at which a given individual's serostatus reached a 50% probability of seronegativity was found to be approximately 18-20 years depending on the annual measles force of infection. Interpretation: Our findings highlight a significant measles immunity gap in young adults aged 20-26 years, posing an increased risk of transmission. A MCV3 at the age of 18-20 years potentially closes the gap and aids measles elimination programmes. Funding: This work was supported by Faculty of Tropical Medicine (MCTM, ICTM grant), Mahidol University (to T.N.) and APC fee was supported by Mahidol University (to T.N.). S.M. and W.P. were funded in whole, or in part, by the Wellcome Trust [Grant number 220211]. For the purpose of open access, the authors have applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission.

Indexed as

Immunity gapsMeaslesMeasles vaccineSeropositivityThird dose measles vaccine

Identifiers

PMID39811540
PMCPMC11732191

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