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一种新的选择:抑制 IgA 肾病患者的补体激活。

A new alternative: inhibiting complement activation in patients with IgA nephropathy.

机构信息

Division of Nephrology and Immunology, RWTH University of Aachen, Aachen, Germany.

出版信息

Kidney Int. 2024 Jan;105(1):28-30. doi: 10.1016/j.kint.2023.10.012.

Abstract

Mesangial complement C3 deposits, reflecting alternative and possibly lectin pathway activation, are characteristic in biopsies of patients with IgA nephropathy (IgAN). A recent randomized controlled trial tested the efficacy and safety of iptacopan, a factor B inhibitor, in patients with IgAN. Iptacopan dose-dependently reduced proteinuria, and there was a pronounced decrease of urinary C5b-9. This offers the perspective of "personalizing" therapy, which would be a unique feature of this novel approach to IgAN. A phase III clinical trial (APPLAUSE-IgAN) is ongoing.

摘要

系膜补体 C3 沉积反映替代途径和(或)凝集素途径的激活,是 IgA 肾病(IgAN)患者活检的特征。最近一项随机对照试验测试了因子 B 抑制剂伊帕替尼在 IgAN 患者中的疗效和安全性。伊帕替尼呈剂量依赖性降低蛋白尿,尿 C5b-9 显著减少。这提供了“个体化”治疗的前景,这将是这种新型 IgAN 治疗方法的独特特征。一项 III 期临床试验(APPLAUSE-IgAN)正在进行中。

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