Advancements in age-related macular degeneration treatment: From traditional anti-VEGF to emerging therapies in gene, stem cell, and nanotechnology

IF 5.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY Biochemical pharmacology Pub Date : 2025-03-28 DOI:10.1016/j.bcp.2025.116902
Zhanfei Wang , Yaqin Zhang , Chunxiu Xu , Anna Peng , Huan Qin , Kai Yao
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Abstract

Age-related macular degeneration (AMD) is the leading cause of central vision loss in older adults and is projected to affect approximately 400 million individuals worldwide by 2040. Its pathological characteristics include retinal extracellular deposits, such as drusen, which trigger photoreceptor degeneration and damage to the retinal pigment epithelium (RPE), resulting in irreversible vision loss. The pathogenesis of AMD involves genetic, environmental, and aging-related factors. Anti-vascular endothelial growth factor (anti-VEGF) therapy for wet AMD significantly inhibits choroidal neovascularization and delays visual deterioration. However, its high cost, frequent injections, and poor patient compliance limit application, and there remains no effective intervention for dry AMD. In recent years, emerging strategies, such as gene therapy, stem cell therapy, and nanotechnology-based drug delivery systems, offer hope for slowing disease progression by improving targeting, drug stability, and reducing treatment frequency. Nanoparticles, including polymeric and lipid systems, have shown promise for enhancing drug delivery and bioavailability, particularly for dry AMD, where existing therapies are inadequate. These strategies also have the potential to improve patient compliance. This review summarizes AMD epidemiology and examines the limitations of current therapies. It emphasizes the mechanisms and clinical advancements of gene therapy, stem cell therapy, and nanotechnology in AMD treatment. These emerging technologies offer promising opportunities for precision medicine and lay a solid foundation for the future development of multifaceted therapeutic strategies.

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年龄相关性黄斑变性治疗的进展:从传统的抗vegf到基因、干细胞和纳米技术的新兴疗法。
老年性黄斑变性(AMD)是老年人中枢视力丧失的主要原因,预计到2040年全球将有大约4亿人受到影响。其病理特征包括视网膜细胞外沉积,如drusen,引发光感受器变性和视网膜色素上皮(RPE)损伤,导致不可逆的视力丧失。AMD的发病机制涉及遗传、环境和衰老相关因素。抗血管内皮生长因子(anti-VEGF)治疗湿性AMD可显著抑制脉络膜新生血管,延缓视力恶化。然而,其成本高,注射频繁,患者依从性差限制了其应用,并且仍然没有有效的干预干性AMD。近年来,诸如基因治疗、干细胞治疗和基于纳米技术的药物传递系统等新兴策略,通过改善靶向性、药物稳定性和减少治疗频率,为减缓疾病进展提供了希望。纳米颗粒,包括聚合物和脂质系统,已经显示出增强药物传递和生物利用度的希望,特别是对于现有治疗方法不足的干性AMD。这些策略也有可能提高患者的依从性。本文综述了AMD的流行病学,并探讨了目前治疗方法的局限性。重点介绍了基因治疗、干细胞治疗和纳米技术在AMD治疗中的作用机制和临床进展。这些新兴技术为精准医疗提供了有希望的机会,并为多方面治疗策略的未来发展奠定了坚实的基础。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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