Evidence map›Paper›PMID 39905573›Full record

ArticleMicrobiome2025

Quantitative profiling of the vaginal microbiota improves resolution of the microbiota-immune axis.

Eric Armstrong, Rachel Liu, James Pollock, Sanja Huibner, Suji Udayakumar, Erastus Irungu, Pauline Ngurukiri, Peter Muthoga, Wendy Adhiambo, Sergey Yegorov and 4 more

Abstract read
In one paragraph

Article in Microbiome, 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

14 authors.

Eric ArmstrongToronto General Hospital Research Institute, University Health Network, Toronto, Canada. eric.armstrong@uhn.ca.
Rachel LiuDepartment of Medicine, University of Toronto, Toronto, Canada.
James PollockDepartment of Immunology, University of Toronto, Toronto, Canada.
Sanja HuibnerDepartment of Medicine, University of Toronto, Toronto, Canada.
Suji UdayakumarDepartment of Medicine, University of Toronto, Toronto, Canada.
Erastus IrunguPartners for Health and Development in Africa (PHDA), Nairobi, Kenya.
Pauline NgurukiriPartners for Health and Development in Africa (PHDA), Nairobi, Kenya.
Peter MuthogaPartners for Health and Development in Africa (PHDA), Nairobi, Kenya.
Wendy AdhiamboPartners for Health and Development in Africa (PHDA), Nairobi, Kenya.
Sergey YegorovDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.
Joshua KimaniPartners for Health and Development in Africa (PHDA), Nairobi, Kenya.
Tara BeattieDepartment of Global Health and Development, London School of Hygiene and Tropical Medicine, London, UK.
Bryan Coburn *Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
Rupert Kaul *Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.

Funding

CIHR Canada Graduate ScholarshipCIHR PJT-180629CIHR Vanier Canada Graduate ScholarshipMedical Research Council and the UK Foreign, Commonwealth and Development Office MR/R023182/1
6 · The paper itself

Abstract

backgroundThe composition of the vaginal microbiota is closely linked to adverse sexual and reproductive health outcomes, due in part to effects on genital immunology. Compositional approaches such as metagenomic sequencing provide a snapshot of all bacteria in a sample and have become the standard for characterizing the vaginal microbiota, but only provide microbial relative abundances. We hypothesized that the addition of absolute abundance data would provide a more complete picture of host-microbe interactions in the female genital tract.

resultsWe analyzed cervicovaginal secretions from 196 female sex workers in Kenya and found that bacterial load was elevated among women with diverse, bacterial vaginosis (BV)-type microbiota and lower among women with Lactobacillus predominance. Bacterial load was also positively associated with proinflammatory cytokines, such as IL-1α, and negatively associated with chemokines, such as IP-10. The associations between bacterial load and immune factors differed across bacterial community states, but L. crispatus predominance was the only microbial community where higher bacterial load was not associated with higher proinflammatory cytokines. Total vaginal bacterial load was also a stronger predictor of the genital immune environment than BV by Nugent score, the current clinical standard, in the Kenya-based cohort and in a Uganda-based confirmatory cohort.

conclusionsOur results suggest that total vaginal bacterial load is at least as strong a predictor of the genital immune milieu as current BV clinical diagnostic tools, supporting exploration of the vaginal bacterial load as a predictor of adverse reproductive and sexual health outcomes. Video Abstract.

Indexed as

BacteriaMicrobiotaVaginaVaginosis, BacterialAdultBacterial LoadCytokinesFemaleHost Microbial InteractionsHumansKenyaSex WorkersUgandaYoung AdultCytokines

Identifiers

PMID39905573
PMCPMC11792376

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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.