一种新型的双特异性抗il - 17/VEGF融合陷阱对年龄相关性黄斑变性的发展具有有效和持久的抑制作用。

IF 2.9 Q2 BIOCHEMICAL RESEARCH METHODS Biochemistry Research International Pub Date : 2024-12-21 eCollection Date: 2024-01-01 DOI:10.1155/bri/1405338
Lan Deng, Lihua Wang, Yun Meng, Jidai Zheng, Xia Dong, Ying Chen, Haomin Huang
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引用次数: 0

摘要

老年性黄斑变性(AMD)是一种严重的眼科疾病,多发于 60 岁及以上的人群。虽然抗血管内皮生长因子疗法在临床上能有效治疗新生血管性黄斑变性(NvAMD),但多达 60% 的患者对疗法没有完全反应。最近的研究表明,血源性巨噬细胞及其相关的促炎细胞因子可能在顽固性疾病的发展和抗血管内皮生长因子疗法的抗药性方面发挥重要作用。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,它能同时抑制 IL-17 诱导的炎症和血管内皮生长因子介导的新生血管。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 在体内的抑制作用比康柏西汀更强更持久。因此,我们为治疗对抗血管内皮生长因子疗法不敏感的老年性黄斑变性患者提供了一种新颖而有前景的策略。
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A Novel Bispecific Anti-IL17/VEGF Fusion Trap Exhibits Potent and Long-Lasting Inhibitory Effects on the Development of Age-Related Macular Degeneration.

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.

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来源期刊
Biochemistry Research International
Biochemistry Research International BIOCHEMICAL RESEARCH METHODS-
CiteScore
6.30
自引率
0.00%
发文量
27
审稿时长
14 weeks
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