Level C· Early human research exploring benefitsProspective StudyEurope PMCOpen access

The exosomal miR-26b-3p derived from Crohn's disease-associated mesenteric adipose tissue induces M1 macrophage polarization and exacerbates ileocolonic anastomosis inflammation via the p38-MAPK signaling pathway

Wu E., Qian W., Zhang X., Gu L., Guo Z., Yu Z.

Prospective Study on Chronic Inflammation, Autoimmune Research, published in Front Immunol (2026) — summary generated from the PubMed abstract.

Open my reading list
Level C· Early human research exploring benefitsEvidence level of this study

Early human evidence such as case series or small samples is exploring possible benefits.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Prospective Study
Journal
Front Immunol (2026)
Reported sample size
—
Source database
Europe PMC
PMID
41822508
PMCID
PMC12975433
DOI
10.3389/fimmu.2026.1754302
Citations
1

Abstract (original English)

Purpose Crohn's Disease (CD) is a chronic inflammatory condition characterized by intestinal inflammation, especially in the progression of postoperative anastomotic recurrence. Recent evidence implicates mesenteric adipose tissue (MAT) in CD pathogenesis, particularly through its exosome secretion, which may influence inflammation pathways. The molecular mechanisms driving this inflammation remain inadequately understood. Methods Exosomes were isolated from MAT of the diseased bowel and macroscopically normal MAT from the surgical margins of patients with CD. We induced chronic intestinal inflammation in mice using dinitrobenzene sulfonic acid (DNBS), simulating CD-like MAT. Using a surgical model of IL10-knockout mice, we performed a series of experiments in vitro and in vivo to assess the effects of exosomes on ileocolonic anastomosis inflammation and macrophage M1 polarization. We performed microRNA microarray analysis, colonoscopy, Western blotting, luciferase assays, and immunofluorescence to investigate the underlying mechanisms. Results Hypertrophic MAT-Exosomes (Ht-exos) promoted ileocolonic anastomotic inflammation by activating macrophage M1 polarization in CD. In vivo , injection of Ht-exos induced inflammatory tissue damage and macrophage M1 polarization in an IL-10 -/- mouse model of ileocecal resection. In vitro , Ht-exos was found to promote macrophage inflammat

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Early human evidence such as case series or small samples is exploring possible benefits.

How we grade evidence
IleumAdipose TissueMacrophagesAnimalsMice, Inbred C57BLMice, KnockoutHumansMiceCrohn DiseaseDisease Models, Animal

Browse all related research

Filter the research library by this study's title keywords, author, or publication year.

Related research