Deng Lan, Wang Lihua, Meng Yun, Zheng Jidai, Dong Xia, Chen Ying, Huang Haomin
Development of Research and Development, Sunshine Guojian Pharmaceutical (Shanghai) Co. Ltd., a 3SBio Inc. Company, 399 Libing Road, Shanghai 201203, China.
Biochem Res Int. 2024 Dec 21;2024:1405338. doi: 10.1155/bri/1405338. eCollection 2024.
Age-related macular degeneration (AMD) is a severe eye disease in people aged 60 years and older. Although anti-VEGF therapies are effective in treating neovascular AMD (NvAMD) in the clinic, up to 60% of patients do not completely respond to the therapies. Recent studies have shown that blood-derived macrophages and their associated proinflammatory cytokines may play important roles in the development of persistent disease and resistance to anti-VEGF therapy. To address this issue, we constructed an antibody-based bispecific fusion protein that can simultaneously inhibit IL-17-induced inflammation and VEGF-mediated neovascularization. As a result, the bispecific fusion protein 17V05 effectively inhibited multiple proinflammatory cytokines and chemokines, as well as laser-induced choroidal neovascularization (CNV). More importantly, 17V05 also exhibited stronger and longer inhibitory effects than conbercept in vivo. Thus, we provide a novel and promising strategy for treating AMD patients who are not sensitive to anti-VEGF therapies.
年龄相关性黄斑变性(AMD)是一种发生于60岁及以上人群的严重眼部疾病。尽管抗血管内皮生长因子(VEGF)疗法在临床上对治疗新生血管性AMD(NvAMD)有效,但高达60%的患者对这些疗法没有完全反应。最近的研究表明,血液来源的巨噬细胞及其相关的促炎细胞因子可能在持续性疾病的发展和对抗VEGF治疗的耐药性中起重要作用。为了解决这个问题,我们构建了一种基于抗体的双特异性融合蛋白,它可以同时抑制白细胞介素-17(IL-17)诱导的炎症和VEGF介导的新生血管形成。结果,双特异性融合蛋白17V05有效抑制了多种促炎细胞因子和趋化因子,以及激光诱导的脉络膜新生血管(CNV)。更重要的是,17V05在体内也表现出比康柏西普更强、更持久的抑制作用。因此,我们为治疗对抗VEGF疗法不敏感的AMD患者提供了一种新的、有前景的策略。