Department of Ophthalmology, Eugene and Marilyn Glick Eye Institute, Indiana University, Indianapolis, IN, USA.
Clearside Biomedical, Inc., Alpharetta, GA, USA.
Expert Opin Investig Drugs. 2020 Mar;29(3):237-244. doi: 10.1080/13543784.2020.1723078. Epub 2020 Jan 31.
: Plasma kallikrein is a mediator of vascular leakage and inflammation. Activation of plasma kallikrein can induce features of diabetic macular edema (DME) in preclinical models. Human vitreous shows elevated plasma kallikrein levels in patients with DME. Because of the incomplete response of some patients to anti-VEGF agents, and the treatment burden associated with frequent dosing, there is still considerable need for VEGF-independent targeted pathways.: This review covers the role of plasma kallikrein in the pathogenesis of DME and the therapeutic potential of plasma kallikrein inhibitors. It discusses early clinical studies of plasma kallikrein pathway modulation for DME, which have been associated with some improvement in visual acuity but with limited improvement in macular edema. This review also highlights KVD001, which is furthest along the development pathway, THR-149, which has recently completed a phase 1 study, and oral agents under development.: Plasma kallikrein inhibitors have a potential role in the treatment of DME, with mixed functional/anatomic results in early clinical trials. Given the large unmet need in DME treatment, further studies are warranted.
血浆激肽释放酶是血管渗漏和炎症的介质。在临床前模型中,血浆激肽释放酶的激活可诱导糖尿病性黄斑水肿(DME)的特征。患有 DME 的患者的人玻璃体中显示血浆激肽释放酶水平升高。由于一些患者对抗 VEGF 药物的反应不完全,并且与频繁给药相关的治疗负担,因此仍然非常需要非 VEGF 依赖性靶向途径。
这篇综述涵盖了血浆激肽释放酶在 DME 发病机制中的作用以及血浆激肽释放酶抑制剂的治疗潜力。它讨论了早期关于 DME 血浆激肽释放酶途径调节的临床研究,这些研究与视力的某些改善相关,但对黄斑水肿的改善有限。该综述还强调了开发途径中进展最快的 KVD001、最近完成了 1 期研究的 THR-149 以及正在开发的口服药物。
血浆激肽释放酶抑制剂在 DME 治疗中具有潜在作用,早期临床试验的功能/解剖结果混合。鉴于 DME 治疗存在巨大的未满足需求,需要进一步研究。