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Recent advances in engineered exosome-based therapies for ocular vascular disease
Jian Guan1, Fanhe Meng2, Chuanzhuo Wang2
1Ophthalmology Department, The First Hospital of China Medical University, Liaoning, 110001, China.
Journal of Nanobiotechnology
|July 19, 2025
Summary
Exosomes show promise for treating ocular neovascular diseases (ONDs) like AMD and DR by overcoming limitations of current anti-VEGF therapies. Further research into large-scale production and safety is needed for clinical use.
Area of Science:
- Ophthalmology
- Regenerative Medicine
- Nanotechnology
Background:
- Ocular neovascular diseases (ONDs), including corneal neovascularization (CoNV), age-related macular degeneration (AMD), and diabetic retinopathy (DR), are leading causes of global vision impairment.
- Current treatments like anti-vascular endothelial growth factor (anti-VEGF) injections have limitations including drug resistance and frequent administration.
Purpose of the Study:
- To review advancements in using exosomes as drug delivery platforms for ONDs.
- To explore the mechanisms by which exosomes modulate ocular angiogenesis, inflammation, and repair.
- To address challenges and future perspectives for clinical translation of exosome-based therapies.
Main Methods:
- Critical review of recent scientific literature on exosome applications in ocular neovascular diseases.
- Analysis of exosome properties, including biocompatibility, low immunogenicity, and targeting capabilities.
- Examination of mechanistic roles in angiogenesis, inflammation, and tissue repair.
Main Results:
- Exosomes serve as effective natural carriers for bioactive molecules, offering advantages over conventional therapies.
- Exosomes demonstrate potential in modulating key pathological processes in ONDs.
- Significant challenges remain, including scalable production, regulatory approval, and safety validation.
Conclusions:
- Exosomes represent a promising innovative therapeutic strategy for ONDs, potentially revolutionizing treatment.
- Overcoming production and regulatory hurdles is crucial for clinical translation.
- Future research should focus on integrated and personalized exosome-based therapies.
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