Guan Jian, Meng Fanhe, Wang Chuanzhuo, Zhang Binglun, Chen Jun, Han Jingnan
Ophthalmology Department, The First Hospital of China Medical University, Liaoning, 110001, China.
Shengjing Hospital of China Medical University, Liaoning, 110004, China.
J Nanobiotechnology. 2025 Jul 19;23(1):526. doi: 10.1186/s12951-025-03589-3.
Ocular neovascular diseases (ONDs), including corneal neovascularization (CoNV), age-related macular degeneration (AMD) and diabetic retinopathy (DR), are among the leading causes of visual impairment worldwide. Current therapeutic strategies predominantly involve intravitreal injection of anti-vascular endothelial growth factor (anti-VEGF) agents, which, despite their efficacy, present significant limitations such as drug resistance, frequent intravitreal injections, and insufficient addressing of underlying pathological mechanisms. This review critically examines recent advancements in the application of exosomes as innovative drug delivery platforms for treating ocular neovascular diseases. Exosomes, naturally occurring extracellular vesicles, exhibit superior biocompatibility, low immunogenicity, and intrinsic targeting capabilities, making them ideal carriers for bioactive molecules including proteins, RNAs, and small drugs. We explore the mechanistic roles of exosomes in modulating pathological angiogenesis, inflammation, and tissue repair within the ocular environment. Additionally, this review addresses the current challenges hindering the clinical translation of these exosomes, including large-scale production, regulatory hurdles, and safety concerns. Future perspectives highlight the potential integration of nanoparticles and exosomes with existing therapies, the development of multifunctional and personalized treatment strategies, and the necessity for standardized protocols to facilitate their transition from bench to bedside. By overcoming these challenges, exosomes hold the promise of revolutionizing the therapeutic landscape for ocular neovascular diseases, ultimately enhancing patient outcomes and quality of life.
眼部新生血管疾病(ONDs),包括角膜新生血管化(CoNV)、年龄相关性黄斑变性(AMD)和糖尿病性视网膜病变(DR),是全球视力损害的主要原因之一。目前的治疗策略主要包括玻璃体内注射抗血管内皮生长因子(anti-VEGF)药物,尽管这些药物有效,但存在显著局限性,如耐药性、频繁的玻璃体内注射以及对潜在病理机制的处理不足。本综述批判性地审视了外泌体作为治疗眼部新生血管疾病的创新药物递送平台的应用方面的最新进展。外泌体是天然存在的细胞外囊泡,具有卓越的生物相容性、低免疫原性和内在靶向能力,使其成为包括蛋白质、RNA和小分子药物在内的生物活性分子的理想载体。我们探讨了外泌体在调节眼部环境中的病理性血管生成、炎症和组织修复方面的机制作用。此外,本综述还讨论了阻碍这些外泌体临床转化的当前挑战,包括大规模生产、监管障碍和安全性问题。未来展望强调了纳米颗粒和外泌体与现有疗法潜在整合的可能性、多功能和个性化治疗策略的发展,以及制定标准化方案以促进其从实验室到临床应用转化的必要性。通过克服这些挑战,外泌体有望彻底改变眼部新生血管疾病的治疗格局,最终改善患者的治疗效果和生活质量。