Evidence map›Paper›PMID 40533059›Full record

ArticleJournal of advanced research2026

Lactobacillus johnsonii-derived extracellular vesicles carrying GAPDH protect against ulcerative colitis through modulating macrophage polarization.

Shiyu Tao, Mengzhen Song, Jinping Fan, Feng Zhu, Tengfei Lv, Hong Wei

Abstract read
In one paragraph

Article in Journal of advanced research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Applied and environmental microbiology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. International journal of nanomedicine · 2026
    Article
  11. Review
  12. Article
  13. Strain-resolved biology ofFrontiers in veterinary science · 2026
    Review
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

6 authors.

Shiyu TaoCollege of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Mengzhen SongCollege of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Jinping FanCollege of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Feng ZhuJinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China.
Tengfei LvJinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing 210000, China. Electronic address: itengfeilv@163.com.
Hong WeiCollege of Animal Sciences and Technology, Huazhong Agricultural University, Wuhan 430070, China. Electronic address: weihong63528@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionUlcerative colitis (UC) is a major inflammatory condition worldwide.

objectivesThe purpose of this study was to investigate the potential contribution of Lactobacillus johnsonii against UC from the perspective of gut microbiota-macrophage-host interactions.

methodsL. johnsonii abundance in UC patients and colitis mice was evaluated by genomic sequencing. SPF and macrophage-depleted mice were employed to explore the effects of L. johnsonii and its products on colitis. An in vitro macrophage and intestinal epithelial cell co-culture system was constructed. Proteins in extracellular vesicles (EVs) were identified by proteomic analyses, and host signaling pathways were analyzed with transcriptomic analyses.

resultsL. johnsonii abundance was found to be associated with macrophage polarization and intestinal barrier function in human UC patients and mice of a colitis model. L. johnsonii and its derived EVs alleviate colitis in mice in a macrophage-dependent manner. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), a protein in EVs derived from L. johnsonii, counteracts colitis in vitro and in vivo by regulating macrophage phenotype. GAPDH enhances anti-inflammatory macrophage polarization by inhibiting the MAPK-STAT3 axis. Macrophage-secreted EVs enhances intestinal barrier function in colitis mice by blocking the TLR4 pathway. Protein components in macrophage-derived EVs contribute to colitis remission and intestinal barrier protection.

conclusionGAPDH originating in L. johnsonii-derived EVs alleviates colitis and improves intestinal barrier by inhibiting STAT3 in macrophages. EVs created from L. johnsonii are a potential novel treatment strategy for UC.

Indexed as

Colitis, UlcerativeExtracellular VesiclesGlyceraldehyde-3-Phosphate DehydrogenasesLactobacillus johnsoniiMacrophagesAnimalsDisease Models, AnimalFemaleGastrointestinal MicrobiomeHumansIntestinal MucosaMacrophage ActivationMaleMiceMice, Inbred C57BLSignal TransductionGlyceraldehyde-3-Phosphate DehydrogenasesToll-Like Receptor 4Extracellular vesiclesGlyceraldehyde-3-phosphate dehydrogenaseLactobacillus johnsoniiMacrophageUlcerative colitis

Identifiers

PMID40533059
PMCPMC12958211

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.