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色素上皮衍生因子在视网膜退行性和血管性疾病中的功能作用:一项范围综述

Functional Roles of Pigment Epithelium-Derived Factor in Retinal Degenerative and Vascular Disorders: A Scoping Review.

作者信息

Jakobsen Thomas Stax, Adsersen Rikke L, Askou Anne Louise, Corydon Thomas J

机构信息

Department of Biomedicine, Aarhus University, Aarhus C, Denmark.

Department of Ophthalmology, Aarhus University Hospital, Aarhus N, Denmark.

出版信息

Invest Ophthalmol Vis Sci. 2024 Dec 2;65(14):41. doi: 10.1167/iovs.65.14.41.

Abstract

PURPOSE

This review explores the role of pigment epithelium-derived factor (PEDF) in retinal degenerative and vascular disorders and assesses its potential both as an adjunct to established vascular endothelial growth factor inhibiting treatments for retinal vascular diseases and as a neuroprotective therapeutic agent.

METHODS

A comprehensive literature review was conducted, focusing on the neuroprotective and anti-angiogenic properties of PEDF. The review evaluated its effects on retinal health, its dysregulation in ocular disorders, and its therapeutic application in preclinical models. Advances in drug delivery, including gene therapy, were also examined.

RESULTS

PEDF, initially identified for promoting neuronal differentiation, is also a potent endogenous angiogenesis inhibitor. Strong anti-angiogenic and neuroprotective effects are observed in preclinical studies. It has pro-apoptotic and antiproliferative effects on endothelial cells thereby reducing neovascularization. Although promising, clinical development is limited with only a single conducted phase I clinical trial for macular neovascularization. Development of PEDF-derived peptides enhances potency and specificity, and emerging gene therapy approaches offer sustained PEDF expression for long-term treatment. However, questions regarding dosage, durability, and efficacy remain, particularly in large animal models.

CONCLUSIONS

PEDF shows significant therapeutic potential in preclinical models of retinal degeneration and vascular disorders. Despite inconclusive evidence on PEDF downregulation as a primary disease driver, many studies highlight its therapeutic benefits and favorable safety profile. Advances in gene therapy could enable long-acting PEDF-based treatments, but further research is needed to optimize dosage and durability, potentially leading to clinical trials and expanding treatment options for retinal disorders.

摘要

目的

本综述探讨色素上皮衍生因子(PEDF)在视网膜退行性疾病和血管疾病中的作用,并评估其作为视网膜血管疾病已确立的血管内皮生长因子抑制治疗辅助药物以及神经保护治疗药物的潜力。

方法

进行了全面的文献综述,重点关注PEDF的神经保护和抗血管生成特性。该综述评估了其对视网膜健康的影响、在眼部疾病中的失调情况以及在临床前模型中的治疗应用。还研究了包括基因治疗在内的药物递送进展。

结果

PEDF最初因促进神经元分化而被发现,也是一种有效的内源性血管生成抑制剂。在临床前研究中观察到了强大的抗血管生成和神经保护作用。它对内皮细胞具有促凋亡和抗增殖作用,从而减少新生血管形成。尽管前景广阔,但临床开发有限,仅针对黄斑新生血管化进行了一项I期临床试验。PEDF衍生肽的开发提高了效力和特异性,新兴的基因治疗方法可实现PEDF的持续表达以进行长期治疗。然而,关于剂量、持久性和疗效的问题仍然存在,尤其是在大型动物模型中。

结论

PEDF在视网膜变性和血管疾病的临床前模型中显示出显著的治疗潜力。尽管关于PEDF下调作为主要疾病驱动因素的证据尚无定论,但许多研究强调了其治疗益处和良好的安全性。基因治疗的进展可能使基于PEDF的长效治疗成为可能,但需要进一步研究以优化剂量和持久性,这可能会促成临床试验并扩大视网膜疾病的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50b2/11684118/3f699786bf48/iovs-65-14-41-f001.jpg

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