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视网膜治疗干预的新领域:新方法的批判性分析。

New frontiers of retinal therapeutic intervention: a critical analysis of novel approaches.

机构信息

Doheny Eye Institute, Pasadena, CA, USA.

Department of Ophthalmology, David Geffen School of Medicine, University of California-Los Angeles, Los Angeles, CA, USA.

出版信息

Ann Med. 2022 Dec;54(1):1067-1080. doi: 10.1080/07853890.2022.2066169.

Abstract

A recent wave of pharmacologic and technologic innovations has revolutionized our management of retinal diseases. Many of these advancements have demonstrated efficacy and can increase the quality of life while potentially reducing complications and decreasing the burden of care for patients. Some advances, such as longer-acting anti-vascular endothelial growth factor agents, port delivery systems, gene therapy, and retinal prosthetics have been approved by the US Food and Drug Administration, and are available for clinical use. Countless other therapeutics are in various stages of development, promising a bright future for further improvements in the management of the retinal disease. Herein, we have highlighted several important novel therapies and therapeutic approaches and examine the opportunities and limitations offered by these innovations at the new frontier. KEY MESSAGESNumerous pharmacologic and technologic advancements have been emerging, providing a higher treatment efficacy while decreasing the burden and associated side effects.Anti-vascular endothelial growth factor (anti-VEGF) and its longer-acting agents have dramatically improved visual outcomes and have become a mainstay treatment in various retinal diseases.Gene therapy and retinal prosthesis implantation in the treatment of congenital retinal dystrophy can accomplish the partial restoration of vision and improved daily function in patients with blindness, an unprecedented success in the field of retina.

摘要

近年来,药理学和技术创新的浪潮彻底改变了我们对视网膜疾病的治疗方法。其中许多进展已经证明了其疗效,可以提高生活质量,同时有可能减少并发症,降低患者的护理负担。一些进展,如长效抗血管内皮生长因子药物、经皮输送系统、基因治疗和视网膜假体,已经获得美国食品和药物管理局的批准,可用于临床应用。无数其他疗法正在不同的开发阶段,为视网膜疾病的进一步治疗改善提供了光明的前景。在此,我们重点介绍了几种重要的新型疗法和治疗方法,并探讨了这些创新在新前沿带来的机遇和局限性。

关键信息

大量药理学和技术进步不断涌现,在降低负担和相关副作用的同时,提高了治疗效果。

血管内皮生长因子(VEGF)拮抗剂及其长效制剂显著改善了视力预后,已成为多种视网膜疾病的主要治疗方法。

基因治疗和视网膜假体植入治疗先天性视网膜营养不良,可以使失明患者部分恢复视力和提高日常功能,这在视网膜领域是前所未有的成功。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5a1/9045775/6dfeac9914dd/IANN_A_2066169_F0001_C.jpg

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