SynthesisTranslational vision science & technology2026
Therapeutic Potential of Mesenchymal Stem Cell-Derived Exosomes in Ocular Surface Disorders.
Synthesis in Translational vision science & technology, 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
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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.
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Who cites it
0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The global burden of ocular surface disorders (OSDs), manifesting as progressive visual impairment and chronic discomfort, has driven urgent exploration of regenerative therapeutic strategies. Mesenchymal stem cell-derived exosomes (MSC-Exos) have emerged as promising candidates for OSD treatment, as they exhibit multifaceted therapeutic properties including immunomodulation, antifibrotic activity, and pro-regenerative capacity. This systematic review consolidates current understanding of MSC-Exo-mediated ocular surface repair mechanisms, with particular emphasis on the molecular dialog established through delivery of bioactive cargo that modulate pivotal signaling pathways. We critically analyze preclinical evidence demonstrating therapeutic efficacy across diverse OSD pathologies, including dry eye disease, corneal epithelial defects, and limbal stem cell deficiency. Notwithstanding these advances, critical barriers to clinical translation persist: (1) methodological heterogeneity arising from variable cell sourcing, culture protocols, and exosome isolation/characterization standards; (2) discordance between animal models and human OSD pathophysiology; and (3) technological limitations in scalable, clinically compatible delivery systems. Addressing these challenges requires interdisciplinary collaboration to standardize exosome production pipelines and establish robust preclinical validation frameworks, thereby accelerating the transition of MSC-Exo therapies from bench to bedside.
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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 Socratic graph.