C3 肾小球病:一种由替代途径失调介导的肾脏疾病。

Frontiers in nephrology Pub Date : 2024-10-29 eCollection Date: 2024-01-01 DOI:10.3389/fneph.2024.1460146
Karin Heidenreich, Deepti Goel, P S Priyamvada, Sagar Kulkarni, Vipul Chakurkar, Dinesh Khullar, Ravi Singh, Charan Bale, Peter F Zipfel
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摘要

C3 肾小球病(C3G)是一种超罕见的补体介导的肾脏疾病,由近端补体的替代途径(AP)失调引起。因此,补体的所有效应环路都处于活跃状态,并可导致病变,如 C3a 和 C5a 介导的炎症、C3b 的疏松作用、表面 C3b 介导的 AP C3 转化酶组装、C3 裂解产物在肾小球内的沉积以及溶解性 C5b-9/MAC 细胞损伤。最常见的病理机制是有缺陷的慢性替代途径失调,主要发生在血浆中,通常会导致 C3 消耗,以及慢性补体介导的肾小球损伤。C3G 会持续数年,50% 以上的患者会丧失肾功能。C3G 由遗传和自身免疫改变引起。遗传原因包括单个补体基因突变和染色体变异,即影响编码补体调节剂基因的缺失和重复。许多基因畸变会导致 AP C3 转化酶活性增加,这可能是由于调节剂的活性降低、调节剂的活性增加,或编码转化酶成分的基因发生了功能增益突变。C3G 的自身免疫形式也确实存在。自身抗体针对单个补体成分和调节剂,或与暴露在中央替代途径 C3 转化酶中的新表位结合,从而增加酶的活性。C3G 患者常见 AP C3 转化酶过度活跃。鉴于 C3G 是一种由替代途径作用缺陷介导的补体疾病,补体阻断是一种新兴的治疗概念。在此,我们总结了 C3G 的病因和补体抑制的原理,并列出了用于 C3G 最先进临床试验的抑制剂。目前有几种抑制剂正处于二期和三期临床试验阶段,预计在不久的将来就能对 C3G 进行有效治疗。
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C3 glomerulopathy: a kidney disease mediated by alternative pathway deregulation.

C3 glomerulopathy (C3G) is an ultra-rare complement-mediated kidney disease caused by to the deregulation of the alternative pathway (AP) of proximal complement. Consequently, all effector loops of the complement are active and can lead to pathologies, such as C3a- and C5a-mediated inflammation, C3b opsonization, surface C3b-mediated AP C3 convertase assembly, C3 cleavage product deposition in the glomerulus, and lytic C5b-9/MAC cell damage. The most common pathologic mechanisms are defective chronic alternative pathway deregulation, mostly occurring in the plasma, often causing C3 consumption, and chronic complement-mediated glomerular damage. C3G develops over several years, and loss of renal function occurs in more than 50% of patients. C3G is triggered by both genetic and autoimmune alterations. Genetic causes include mutations in individual complement genes and chromosomal variations in the form of deletions and duplications affecting genes encoding complement modulators. Many genetic aberrations result in increased AP C3 convertase activity, either due to decreased activity of regulators, increased activity of modulators, or gain-of-function mutations in genes encoding components of the convertase. Autoimmune forms of C3G do also exist. Autoantibodies target individual complement components and regulators or bind to neoepitopes exposed in the central alternative pathway C3 convertase, thereby increasing enzyme activity. Overactive AP C3 convertase is common in C3G patients. Given that C3G is a complement disease mediated by defective alternative pathway action, complement blockade is an emerging concept for therapy. Here, we summarize both the causes of C3G and the rationale for complement inhibition and list the inhibitors that are being used in the most advanced clinical trials for C3G. With several inhibitors in phase II and III trials, it is expected that effectice treatment for C3G will become availabe in the near future.

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