Evidence mapPaperPMID 41922545Full record

ArticleScientific reports2026

LPS-induced endometrial cell-derived exosomes suppress probiotic Lactobacillus growth.

Le-Ming Wang, Yeu-Ching Shi, Bao-Hong Lee, Ching-Hsuan Liu, El-Wui Loh, Chen-Jei Tai, Liang-Tzung Lin

Abstract read
In one paragraph

Article in Scientific reports, 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

7 authors.

Le-Ming WangGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Yeu-Ching ShiBioX Biotech CO., Ltd., Taipei, Taiwan.
Bao-Hong LeeDepartment of Horticulture, National Chiayi University, Chiayi, Taiwan.
Ching-Hsuan LiuDepartment of Microbiology and Immunology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
El-Wui LohGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Chen-Jei TaiGraduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Liang-Tzung LinDepartment of Microbiology and Immunology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan. ltlin@tmu.edu.tw.

Funding

National Science and Technology Council NSTC 114-2320-B-038-044Wan Fang Hospital 112-wf-phd-01
6 · The paper itself

Abstract

Spontaneous preterm birth (sPTB) has been increasingly associated with alterations in vaginal microbiota. While Lactobacillus spp., which physiologically dominate the cervical microbiota, are considered protective with a lower risk of intra-amniotic infection and chorioamnionitis, other microbes such as Gardnerella vaginalis are associated with an increased risk of sPTB. Although this association is well documented, the host mechanisms that regulate the composition of vaginal microbial communities remain poorly understood. Emerging evidence suggests that host-derived exosomes may play a critical role in shaping the microbial environment. This study hypothesized that endothelial cell-derived exosomes may modulate the growth of probiotic Lactobacillus spp. through changes in microRNA cargo, thereby influencing the risk of sPTB. To investigate this hypothesis, HEC-1-A cells were stimulated with lipopolysaccharides (LPS), and exosomes were isolated from these cells. These exosomes were then applied to four Lactobacillus strains (L. crispatus, L. gasseri, L. jensenii, L. reuteri) to evaluate how LPS-induced alterations in exosomal microRNA content affect probiotic growth. The results indicate that exosomes derived from LPS-stimulated HEC-1-A cells inhibited the four bacterial strains and facilitated the expansion of the opportunistic pathogen G. vaginalis in a mixed-culture system. MicroRNA sequencing revealed that LPS stimulation increased the levels of miR-181d-5p and miR-181c in these exosomes, both of which may contribute to the suppression of Lactobacillus spp. growth. Taken together, these findings suggest a novel regulatory pathway in which host-derived exosomes influence the vaginal microbiota, suggesting that disruptions in this mechanism may contribute to vaginal dysbiosis and increase the risk of sPTB.

Indexed as

EndometriumExosomesLactobacillusLipopolysaccharidesProbioticsCell LineFemaleHumansMicrobiotaMicroRNAsPremature BirthVaginaLipopolysaccharidesMicroRNAsExosomeMicroRNAProbioticSpontaneous preterm birthVaginal microbiota

Identifiers

PMID41922545
PMCPMC13181033

What Socratic holds

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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.