Mesenchymal Stem Cell-Derived Exosomes for Keratoconus: A Novel Therapeutic Approach
Hadi A., Hashemian H., Khorrami-Nejad M., Narooie-Noori F.
Laboratory Study on Chronic Wound, Chronic Inflammation, Immune Modulation, published in J Curr Ophthalmol (2025) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- 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
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
- Laboratory Study
- Journal
- J Curr Ophthalmol (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41982825
- PMCID
- PMC13075913
- DOI
- 10.4103/joco.joco_202_25
Abstract (original English)
Keratoconus (KC) is a progressive corneal ectatic disorder with limited treatment options addressing its underlying pathophysiology. Current therapies, including corneal cross-linking and transplantation, focus on halting progression rather than reversing damage. Mesenchymal stem cell-derived exosomes (MSC-Exo) have emerged as promising cell-free therapeutic agents with regenerative, anti-inflammatory, and immunomodulatory properties. This short communication synthesizes current evidence on MSC-Exo for KC treatment. Preclinical studies demonstrate that MSC-Exo enhances keratocyte proliferation, reduces fibrosis and inflammation, modulates extracellular matrix proteins, and promotes epithelial wound healing. Exosomes from various MSC sources show therapeutic efficacy across in vitro and animal models. While clinical evidence remains limited, early studies support safety and feasibility for ocular applications. MSC-Exo represents a promising therapeutic approach capable of modulating key KC pathological mechanisms, warranting further clinical investigation.
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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