Prunotto Marco, Nachman Patrick H, Gillespie Barbara S, Beck Laurence H, Thompson Aliza M, Hu Austin H, Stafford Elizabeth A, Tarnoff Josh M, Rovin Brad H
School of Pharmaceutical Sciences, Institute of Pharmaceutical Sciences of Western Switzerland, University of Geneva, Geneva, Switzerland.
Division of Renal Diseases and Hypertension, Department of Medicine, University of Minnesota, Minneapolis, MN, USA.
Glomerular Dis. 2025 Mar 14;5(1):133-141. doi: 10.1159/000544808. eCollection 2025 Jan-Dec.
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.
原发性膜性肾病是成人肾病综合征的常见病因,年发病率为每百万人口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M型磷脂酶A2受体1(PLA2R)被确定为疾病自身抗原之前,原发性膜性肾病的自身抗原一直难以捉摸。随后,其他几种自身抗原也相对迅速地被发现。约75%的原发性膜性肾病患者可检测到抗PLA2R自身抗体。针对PLA2R的循环和沉积自身抗体的发现为肾脏病学提供了个性化疾病管理的机会。2023年1月14日,国际肾病治愈组织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研发项目中纳入抗PLA2R自身抗体的相关考量。本报告记录了膜性肾病科学研讨会上的讨论情况。