设计抗磷脂酶A2受体1时代膜性肾病治疗的临床试验:肾治疗膜性肾病研讨会的结果。

Glomerular diseases Pub Date : 2025-03-14 eCollection Date: 2025-01-01 DOI:10.1159/000544808
Marco Prunotto, Patrick H Nachman, Barbara S Gillespie, Laurence H Beck, Aliza M Thompson, Austin H Hu, Elizabeth A Stafford, Josh M Tarnoff, Brad H Rovin
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引用次数: 0

摘要

原发性膜性肾病是成人肾病综合征的常见病因,每年的总发病率为每百万人中有12例。原发性膜性肾病是一种自身免疫性肾脏疾病;然而,直到2009年,当m型磷脂酶A2受体1 (PLA2R)被确定为一种疾病自身抗原时,原发性膜性肾病自身抗原一直难以捉摸。随后很快又发现了其他几种自身抗原。约75%的原发性膜性肾病患者可检测到PLA2R自身抗体。循环和沉积的PLA2R自身抗体的发现为肾病学提供了个性化疾病管理的机会。2023年1月14日,NephCure Kidney International在弗吉尼亚州阿灵顿召开了一次科学研讨会,讨论抗PLA2R自身抗体的科学现状,以及在膜性肾病药物开发项目中结合抗PLA2R自身抗体的相关考虑。本报告记录了在膜性肾病科学研讨会上发生的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Designing Clinical Trials for the Treatment of Membranous Nephropathy in the Anti-Phospholipase A2 Receptor 1 Era: Results of a NephCure Membranous Nephropathy Workshop.

Primary membranous nephropathy is a common cause of adult-onset nephrotic syndrome, with an overall incidence of 12 cases per million per year. Primary membranous nephropathy is an autoimmune kidney disease; however, primary membranous nephropathy autoantigens remained elusive until 2009, when the M-type phospholipase A2 receptor 1 (PLA2R) was identified as a disease autoantigen. This was followed relatively rapidly by the identification of several other autoantigens. Autoantibodies against PLA2R are detectable in ≈75% of patients with primary membranous nephropathy. The discovery of circulating and deposited autoantibodies against PLA2R offers an opportunity in nephrology to personalize disease management. On January 14, 2023, NephCure Kidney International convened a scientific workshop in Arlington, Virginia, to discuss the state of the science on autoantibodies against PLA2R and considerations related to the incorporation of autoantibodies against PLA2R in drug development programs for membranous nephropathy. The present report captures the discussion that occurred at the Membranous Nephropathy Scientific Workshop.

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