Mesenchymal stem cell-derived extracellular vesicles for dry eye disease: principles, progress, and challenges.

IF 8.5
Extracellular vesicles and circulating nucleic acids Pub Date : 2026-06-24 eCollection Date: 2026-01-01 DOI:10.20517/evcna.2025.174
Yuting Feng, Mingqi Zhang
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Abstract

Dry eye disease (DED) is a multifactorial ocular surface disorder characterized by disruption of tear film and/or ocular surface homeostasis that represents a significant global public health concern. This review summarizes the pathogenesis of DED, with particular emphasis on the central role of ocular surface inflammation. It further comprehensively evaluates the therapeutic rationale, preclinical advances, and translational challenges associated with mesenchymal stem cell-derived extracellular vesicle (MSC-EV) therapy for DED. MSC-EVs exhibit numerous properties, including anti-inflammatory, immunomodulatory, reparative, and regenerative effects, and offer key advantages such as a cell-free nature, low immunogenicity, minimal tumorigenic risk, high stability, and suitability for topical administration. Through advanced strategies such as cargo engineering, hybrid design, biomaterial-assisted delivery, and genetic engineering, the therapeutic performance of MSC-EVs can be further optimized, enabling targeted delivery, improved retention and bioavailability, and precise immunomodulation. In addition, three-dimensional ocular surface and ex vivo models help overcome the limitations of traditional animal models in replicating human ocular physiology. Among available sources, umbilical cord-derived MSC-EVs represent one of the most promising candidates for clinical translation. Despite these advances, several challenges remain, including ocular-specific anatomical and physiological barriers, limited pharmacological characterization, lack of standardized large-scale production and storage protocols, incomplete toxicological and microbiological safety evaluation, and the absence of a unified regulatory framework. Overall, MSC-EVs represent a potentially transformative therapeutic strategy for the management of refractory DED. However, as most current evidence remains preclinical, further validation in human-relevant models and clinical studies is essential before definitive conclusions can be drawn.

间充质干细胞衍生的细胞外囊泡治疗干眼病:原理、进展和挑战。
干眼病(DED)是一种以泪膜和/或眼表面稳态破坏为特征的多因素眼表疾病,是一个重大的全球公共卫生问题。本文综述了DED的发病机制,特别强调眼表炎症的中心作用。它进一步全面评估了间充质干细胞衍生的细胞外囊泡(MSC-EV)治疗DED的治疗原理、临床前进展和转化挑战。msc - ev具有许多特性,包括抗炎、免疫调节、修复和再生作用,并具有诸如无细胞性质、低免疫原性、最小致瘤风险、高稳定性和适合局部给药等关键优势。通过货物工程、混合设计、生物材料辅助递送和基因工程等先进策略,msc - ev的治疗性能可以进一步优化,实现靶向递送、提高保留率和生物利用度以及精确的免疫调节。此外,三维眼表和离体模型有助于克服传统动物模型在复制人类眼生理方面的局限性。在现有的来源中,脐带来源的msc - ev是最有希望用于临床转化的候选者之一。尽管取得了这些进展,但仍存在一些挑战,包括眼特异性解剖和生理障碍、有限的药理学表征、缺乏标准化的大规模生产和储存方案、不完整的毒理学和微生物安全性评估以及缺乏统一的监管框架。总的来说,msc - ev代表了难治性DED治疗的潜在变革性治疗策略。然而,由于目前大多数证据仍处于临床前阶段,在得出明确结论之前,必须在与人类相关的模型和临床研究中进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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