Evidence map›Paper›PMID 41388385›Full record

ArticleBMC infectious diseases2025

Evaluating the effectiveness of the 13-valent pneumococcal conjugate vaccine and clinical and demographic characteristics on pneumococcal carriage density in young children in Papua New Guinea, Lao PDR, and Mongolia.

Claire von Mollendorf, Isatou Jagne, Elizabeth A Ashley, Christopher C Blyth, Jocelyn Chan, Rebecca L Ford, Mayfong Mayxay, E Kim Mulholland, Tuya Mungun, Dorj Narangerel and 14 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. 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

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

24 authors.

Claire von Mollendorf *Infection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia. claire.vonmollendorf@mcri.edu.au.
Isatou Jagne *Infection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Elizabeth A AshleyLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Christopher C BlythWesfarmers Centre for Vaccines and Infectious Diseases, The Kids Research Institute Australia, Perth, Australia.
Jocelyn ChanInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Rebecca L FordInfection and Immunity Unit, Papua New Guinea Institute of Medical Research (PNG IMR), Goroka, Papua New Guinea.
Mayfong MayxayLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
E Kim MulhollandInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Tuya MungunNational Center for Communicable Diseases (NCCD), Ulaanbaatar, Mongolia.
Dorj NarangerelMinistry of Health, Ulaanbaatar, Mongolia.
Odgerel TundevNational Center for Communicable Diseases (NCCD), Ulaanbaatar, Mongolia.
Monica L NationInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Cattram D NguyenInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Belinda D OrtikaInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Casey L PellInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Joycelyn SapuraInfection and Immunity Unit, Papua New Guinea Institute of Medical Research (PNG IMR), Goroka, Papua New Guinea.
Keoudomphone VilivongLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
Jana LaiInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Yuhang ZhangDepartment of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia.
David A B DanceLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Mahosot Hospital, Vientiane, Lao People's Democratic Republic.
William S PomatInfection and Immunity Unit, Papua New Guinea Institute of Medical Research (PNG IMR), Goroka, Papua New Guinea.
Catherine SatzkeInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
Fiona M RussellInfection, Immunity and Global Health, Murdoch Children's Research Institute, Parkville, VIC, Australia.
PneuCaPTIVE Research Group

Funding

Bill and Melinda Gates Foundation OPP1115490Wellcome Trust
6 · The paper itself

Abstract

backgroundHigh nasopharyngeal pneumococcal carriage density is associated with severe pneumonia; however, little is known about factors that affect pneumococcal carriage density including pneumococcal vaccination. We describe pneumococcal density by clinical and demographic factors, and effect of 13-valent pneumococcal conjugate vaccine (PCV13) on density in Papua New Guinea (PNG), Lao People’s Democratic Republic (Lao PDR) and Mongolia, 3–6 years following national PCV13 introduction.

methodsThree prospective pneumococcal carriage surveillance studies enrolled children aged 2–59 months with acute respiratory infections in Lao PDR (2013–2019), and pneumonia in PNG (2016–2019) and Mongolia (2015–2019). Demographic and clinical factors were collected on interview and from medical records. Nasopharyngeal swabs were tested for pneumococci using lytA real-time quantitative PCR and molecular serotyping using DNA microarray. In unvaccinated children median pneumococcal carriage density was compared across relevant clinical and demographic factors using Wilcoxon rank sum or Kruskal Wallis tests. Quantile regression models were used to determine the association between pneumococcal density, vaccination status and number of PCV doses.

resultsA total of 1009 (PNG), 532 (Lao PDR) and 621 (Mongolia) pneumococcal carriers were included. Of carriers with serotyping results, PCV13 serotype (VT) carriage was 36.1% (356/985) in PNG, 40.8% (189/463) in Lao PDR and 50.7% (270/532) in Mongolia. The median pneumococcal VT density was 6.25 log10GE/ml (genome equivalents per milliliter) (interquartile range [IQR] 5.66, 6.79) in PNG, 5.74 log10GE/ml (IQR 4.99, 6.40) in Lao PDR and 5.64 log10GE/ml (IQR 5.11, 6.32) in Mongolia. In PNG, Lao PDR and Mongolia, 54.4%, 51.1% and 34.9% pneumococcal carriers were fully vaccinated, respectively. There was no difference in VT pneumococcal density by relevant clinical and demographic factors in unvaccinated children. In PNG, VT density was slightly lower (-0.36, 95% confidence interval [CI] -0.61, -0.12; p = 0.004) among vaccinated compared with unvaccinated children, in particular those who received three doses (-0.37 95% CI -0.63, -0.10; p = 0.007). No differences were observed in Lao PDR and Mongolia.

conclusionsWe demonstrated variable results across our three sites. Indirect PCV13 effects may have resulted in limited observed reductions in VT density in unvaccinated children. In PNG, PCV13 vaccination was associated with a decline in VT density.

trial registrationNot applicable.

Indexed as

Carrier StatePneumococcal InfectionsPneumococcal VaccinesStreptococcus pneumoniaeChild, PreschoolFemaleHumansInfantLaosMaleMongoliaNasopharynxPapua New GuineaProspective StudiesVaccines, Conjugate13-valent pneumococcal vaccinePneumococcal VaccinesVaccines, ConjugateCarriageChildrenPneumococcal conjugate vaccinesPneumococcal nasopharyngeal density

Identifiers

PMID41388385
PMCPMC12821165

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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.