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在肾移植后IgA肾病复发中,iptacopan靶向替代补体途径可消除C3,并显著减少肾小球内C5b - 9的沉积。

Targeting the alternative complement pathway by iptacopan abrogates C3 and strongly reduces C5b-9 deposition within glomeruli in IgA nephropathy recurrence after kidney transplantation.

作者信息

Sanna Enrico, Nicassio Silvia Rita, Mella Alberto, Mingozzi Silvia, Manzione Ana Maria, Dolla Caterina, Gallo Ester, Randone Paolo, Tarragoni Rita, Benetto Giulia, Barreca Antonella, Arato Carlotta, Deambrosis Ilaria, Biancone Luigi

机构信息

Renal Transplantation Center "A. Vercellone," Division of Nephrology, Dialysis and Transplantation, Department of Medical Sciences, Città Della Salute e Della Scienza Hospital and University of Turin, Corso Bramante, 88-10126, Turin, Italy.

Pathology Unit, University of Turin, Città Della Salute e Della Scienza, Turin, Italy.

出版信息

Am J Transplant. 2025 Aug 23. doi: 10.1016/j.ajt.2025.08.015.

Abstract

Current trials are exploring complement blockade in IgA nephropathy (IgAN) of native kidneys. No data are available on IgAN recurrence. Here, we report on the first small case series (n = 5) treated with iptacopan, a factor B inhibitor targeting the alternative complement pathway, for this condition, providing biopsy findings after treatment. All patients underwent indication biopsies for proteinuria increase, graft function deterioration, and subsequent posttreatment biopsies. Three of 5 were treated with iptacopan-only between the biopsies, whereas in 2 of 5, iptacopan treatment was preceded by either a steroid pulse or a steroid pulse plus plasmapheresis. Within 6 to 12 months, iptacopan led to a marked reduction in terminal complement component deposition (C5b-9) and almost disappearance of C3. In contrast, IgA deposition was slightly reduced. There was no consistent improvement in proteinuria. No major adverse events (AE) occurred. In conclusion, to our knowledge, this is the first report of iptacopan use for recurrent IgAN in kidney transplant recipients. In addition, it demonstrates in vivo modulation of glomerular complement deposition, specifically preventing C3 deposition and C5b-9 fixation, which is considered a major effector mechanism of tissue injury. Large cohorts are required to define its impact on clinical outcomes in long-term transplant settings.

摘要

目前的试验正在探索在原发性IgA肾病(IgAN)中进行补体阻断。关于IgAN复发尚无相关数据。在此,我们报告首例小病例系列(n = 5),针对这种情况使用iptacopan(一种靶向替代补体途径的B因子抑制剂)进行治疗,并提供治疗后的活检结果。所有患者均因蛋白尿增加、移植肾功能恶化接受了指征性活检,随后进行了治疗后活检。5例中有3例在两次活检之间仅接受iptacopan治疗,而5例中有2例在iptacopan治疗前接受了类固醇冲击治疗或类固醇冲击治疗加血浆置换。在6至12个月内,iptacopan使终末补体成分沉积(C5b-9)显著减少,C3几乎消失。相比之下,IgA沉积略有减少。蛋白尿无持续改善。未发生重大不良事件(AE)。总之,据我们所知,这是关于肾移植受者复发性IgAN使用iptacopan的首例报告。此外,它证明了肾小球补体沉积的体内调节作用,特别是防止C3沉积和C5b-9固定,这被认为是组织损伤的主要效应机制。需要大型队列研究来确定其在长期移植环境中对临床结局的影响。

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