Mesenchymal Stem Cells Derived Extracellular Vesicles in Inflammatory Bowel Disease: Therapeutic Efficacy and Bioengineering Applications.
Li Z., Sun Y., Wu J., Zhang W., Li T., Tang S.
Narrative Review on Chronic Inflammation, Immune Modulation, published in Int J Nanomedicine (2026) — summary generated from the PubMed abstract.
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
- Narrative Review
- Journal
- Int J Nanomedicine (2026)
- Country
- New Zealand
- Reported sample size
- —
- PMID
- 41993781
- DOI
- 10.2147/IJN.S584494
Abstract (original English)
Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) have emerged as a promising therapeutic approach for inflammatory bowel disease (IBD) due to their anti-inflammatory properties, immune modulation, and tissue regeneration potential. However, challenges in optimizing their production, efficacy, and understanding their therapeutic mechanisms remain. MSC-EVs, particularly those derived from bone marrow and umbilical mesenchymal stem cells, have shown significant therapeutic potential in both preclinical and clinical studies. Although the advantages of MSC-EVs over traditional therapies, such as low immunogenicity and non-invasive administration, limitations in their targeting capabilities and stability in fibrotic tissues impede full clinical translation. This review succinctly outlines a comparative analysis of MSC-EVs derived from various sources, such as bone marrow, adipose tissue, perinatal tissues, dental tissues, olfactory mucosa, and hair follicles in IBD treatment. Additionally, the applications of bioengineered MSC-EVs, including their use as nanodrug carriers and in targeted therapies, are discussed, with an emphasis on the future potential of integrating MSC-EVs with biomaterials like hydrogels. Finally, the current challenges and potential solutions for translating MSC-EVs from bench to bedside are discussed. This review aims to elucidate the therapeutic
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
There is currently not enough data to draw conclusions about benefit or risk for this topic.
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