Yerramothu Praveen
School of Optometry and Vision Science, University of New South Wales, Sydney 00098, Australia.
Vision (Basel). 2018 Jul 30;2(3):31. doi: 10.3390/vision2030031.
Neovascular age-related macular degeneration (nAMD) is one of the leading causes of blindness among the aging population. The current treatment options for nAMD include intravitreal injections of anti-vascular endothelial growth factor (anti-VEGF). However, standardized frequent administration of anti-VEGF injections only improves vision in approximately 30-40% of nAMD patients. Current therapies targeting nAMD pose a significant risk of retinal fibrosis and geographic atrophy (GA) development in nAMD patients. A need exists to develop new therapies to treat nAMD with effective and long-term anti-angiogenic effects. Recent research on nAMD has identified novel therapeutic targets and angiogenic signaling mechanisms involved in its pathogenesis. For example, tissue factor, human intravenous immune globulin, interferon-β signaling, cyclooxygenase-2 (COX-2) and cytochrome P450 monooxygenase lipid metabolites have been identified as key players in the development of angiogenesis in AMD disease models. Furthermore, novel therapies such as NACHT, LRR and PYD domains containing protein 3 (NLRP3) inflammasome inhibition, inhibitors of integrins and tissue factor are currently being tested at the level of clinical trials to treat nAMD. The aim of this review is to discuss the scope for alternative therapies proposed as anti-VEGFs for the treatment of nAMD.
新生血管性年龄相关性黄斑变性(nAMD)是老年人群失明的主要原因之一。目前nAMD的治疗选择包括玻璃体内注射抗血管内皮生长因子(抗VEGF)。然而,标准化的频繁抗VEGF注射仅能使约30-40%的nAMD患者视力得到改善。目前针对nAMD的治疗方法在nAMD患者中存在视网膜纤维化和地理性萎缩(GA)发展的重大风险。因此,需要开发具有有效和长期抗血管生成作用的新疗法来治疗nAMD。最近对nAMD的研究已经确定了其发病机制中涉及的新治疗靶点和血管生成信号机制。例如,在AMD疾病模型中,组织因子、人静脉注射免疫球蛋白、干扰素-β信号传导、环氧合酶-2(COX-2)和细胞色素P450单加氧酶脂质代谢产物已被确定为血管生成发展的关键因素。此外,诸如含NACHT、LRR和PYD结构域蛋白3(NLRP3)炎性小体抑制、整合素抑制剂和组织因子等新疗法目前正在临床试验阶段进行测试以治疗nAMD。本综述的目的是讨论作为抗VEGF药物用于治疗nAMD的替代疗法的应用范围。