Recent advances in engineered exosome-based therapies for ocular vascular disease.

IF 10.6 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jian Guan, Fanhe Meng, Chuanzhuo Wang, Binglun Zhang, Jun Chen, Jingnan Han
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Abstract

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.

基于工程外泌体的眼部血管疾病治疗的最新进展。
包括角膜新生血管(CoNV)、年龄相关性黄斑变性(AMD)和糖尿病性视网膜病变(DR)在内的眼部新生血管疾病(ond)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,但存在明显的局限性,如耐药性、频繁的玻璃体内注射以及对潜在病理机制的研究不足。本文综述了外泌体作为治疗眼部新生血管疾病的创新药物传递平台的最新进展。外泌体是天然存在的细胞外囊泡,具有优越的生物相容性、低免疫原性和内在的靶向能力,使其成为生物活性分子(包括蛋白质、rna和小药物)的理想载体。我们探索外泌体在调节病理性血管生成、炎症和眼内组织修复中的机制作用。此外,本综述还讨论了目前阻碍这些外泌体临床翻译的挑战,包括大规模生产、监管障碍和安全性问题。未来的观点强调纳米颗粒和外泌体与现有疗法的潜在整合,多功能和个性化治疗策略的发展,以及标准化方案的必要性,以促进它们从实验室到床边的过渡。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前景,最终提高患者的治疗效果和生活质量。
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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来源期刊
Journal of Nanobiotechnology
Journal of Nanobiotechnology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
13.90
自引率
4.90%
发文量
493
审稿时长
16 weeks
期刊介绍: Journal of Nanobiotechnology is an open access peer-reviewed journal communicating scientific and technological advances in the fields of medicine and biology, with an emphasis in their interface with nanoscale sciences. The journal provides biomedical scientists and the international biotechnology business community with the latest developments in the growing field of Nanobiotechnology.
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