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增殖性视网膜病变的新型疗法。

Novel therapies for proliferative retinopathies.

作者信息

Martinez-Alejo Juan Manuel, Baiza-Duran Leopoldo Martin, Quintana-Hau Juan de Dios

机构信息

Centro de Investigación Sophia, Laboratorios Sophia SA de CV, Zapopan, Mexico.

Laboratorios Sophia SA de CV, Zapopan, Mexico.

出版信息

Ther Adv Chronic Dis. 2022 Dec 2;13:20406223221140395. doi: 10.1177/20406223221140395. eCollection 2022.

Abstract

Proliferative retinopathies, such as neovascular age-related macular degeneration and proliferative diabetic retinopathy, are a special health issue due to their contribution to irreversible blindness. Although the promoting conditions and physiopathology of proliferative retinopathies are different, these feature a highly detrimental angiogenesis driven by the overproduction of vascular endothelial growth factor (VEGF). This article describes the mechanism of action of ocular antiangiogenic therapies currently found in clinical development. Systems classify accordingly as (a) novel anti-VEGF systems, (b) molecules targeting non-VEGF pathways, and (c) gene therapies. Whereas most therapies are designed to neutralize VEGF, there is a significant set of products with diverse complexity and mechanism of action. Anti-VEGF therapies are still the most studied approach to tackle angiogenesis. Therapies targeting non-VEGF pathways, however, are highlighted because they could be an option for patients nonresponsive to anti-VEGF therapies. Finally, gene therapy is a promissory technology platform but still is subject to demonstrate safety and efficacy.

摘要

增殖性视网膜病变,如新生血管性年龄相关性黄斑变性和增殖性糖尿病视网膜病变,因其会导致不可逆性失明而成为一个特殊的健康问题。尽管增殖性视网膜病变的促发条件和病理生理学有所不同,但它们都具有由血管内皮生长因子(VEGF)过度产生驱动的高度有害的血管生成。本文描述了目前处于临床开发阶段的眼部抗血管生成疗法的作用机制。这些系统相应地分为三类:(a)新型抗VEGF系统,(b)靶向非VEGF途径的分子,以及(c)基因疗法。虽然大多数疗法旨在中和VEGF,但仍有大量具有不同复杂性和作用机制的产品。抗VEGF疗法仍然是研究最多的解决血管生成问题的方法。然而,靶向非VEGF途径的疗法受到关注,因为它们可能为对抗VEGF疗法无反应的患者提供一种选择。最后,基因疗法是一个有前景的技术平台,但仍需证明其安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/736a/9720790/26898209b54e/10.1177_20406223221140395-fig1.jpg

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