ArticleMaterials today. Bio2026
Adhesive cationic hyaluronic acid loading with small extracellular vesicles from IL-6 activated mesenchymal stem cells improves repair of corrosive esophageal injury.
Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
12 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The treatment of corrosive esophageal injury (CEI) remains challenging due to recurrent courses, frequent complications, and severe tissue damage. Enhancing the therapeutic potential of mesenchymal stem cell-derived small extracellular vesicles (sEVs) through cytokine preconditioning has emerged as a promising strategy. In this study, functionally enhanced sEVs (E-sEVs) were generated by pretreating umbilical cord-derived mesenchymal stem cells with interleukin-6 (IL-6). E-sEVs exhibited superior capabilities in promoting fibroblast migration and suppressing macrophage-mediated inflammation compared to naïve sEVs. To improve local retention and therapeutic efficacy, E-sEVs were integrated into a cationic hyaluronic acid (CHA) hydrogel with strong bioadhesive properties, forming a composite system termed E-sEVs@CHA. In vitro assays demonstrated that E-sEVs@CHA effectively promoted endothelial cell invasion, exhibited antioxidant activity, and modulated macrophage polarization toward an anti-inflammatory phenotype. In a rat model of CEI, E-sEVs@CHA significantly reduced esophageal inflammation, oxidative stress, and fibrotic remodeling, leading to improved tissue repair and reduced stricture formation. This study presents a novel cell-free therapeutic strategy with translational potential for the management of corrosive esophageal injury.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.