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感染相关性肾小球肾炎与 C3 肾小球病的临床-病理相似性和差异。

Clinico-Pathogenic Similarities and Differences between Infection-Related Glomerulonephritis and C3 Glomerulopathy.

机构信息

Department of Nephrology, Kitasato University School of Medicine, 1-15-1 Kitasato, Minami-ku, Sagamihara 252-0374, Kanagawa, Japan.

Department of Nephrology and Blood Purification, Kidney Disease Center, Tokyo Medical University Hachioji Medical Center, Hachioji 193-0998, Tokyo, Japan.

出版信息

Int J Mol Sci. 2023 May 8;24(9):8432. doi: 10.3390/ijms24098432.

Abstract

Recently, the comprehensive concept of "infection-related glomerulonephritis (IRGN)" has replaced that of postinfectious glomerulonephritis (PIGN) because of the diverse infection patterns, epidemiology, clinical features, and pathogenesis. In addition to evidence of infection, hypocomplementemia particularly depresses serum complement 3 (C3), with endocapillary proliferative and exudative GN developing into membranoproliferative glomerulonephritis (MPGN); also, C3-dominant or co-dominant glomerular immunofluorescence staining is central for diagnosing IRGN. Moreover, nephritis-associated plasmin receptor (NAPlr), originally isolated from the cytoplasmic fraction of group A , is vital as an essential inducer of C3-dominant glomerular injury and is a key diagnostic biomarker for IRGN. Meanwhile, "C3 glomerulopathy (C3G)", also showing a histological pattern of MPGN due to acquired or genetic dysregulation of the complement alternative pathway (AP), mimics C3-dominant IRGN. Initially, C3G was characterized by intensive "isolated C3" deposition on glomeruli. However, updated definitions allow for glomerular deposition of other complement factors or immunoglobulins if C3 positivity is dominant and at least two orders of magnitude greater than any other immunoreactant, which makes it challenging to quickly distinguish pathomorphological findings between IRGN and C3G. As for NAPlr, it was demonstrated to induce complement AP activation directly in vitro, and it aggravates glomerular injury in the development of IRGN. A recent report identified anti-factor B autoantibodies as a contributing factor for complement AP activation in pediatric patients with PIGN. Moreover, C3G with glomerular NAPlr deposition without evidence of infection was reported. Taken together, the clinico-pathogenic features of IRGN overlap considerably with those of C3G. In this review, similarities and differences between the two diseases are highlighted.

摘要

最近,由于感染模式、流行病学、临床特征和发病机制的多样性,“感染相关性肾小球肾炎(IRGN)”的综合概念已经取代了“感染后肾小球肾炎(PIGN)”。除了感染证据外,低补体血症尤其会使血清补体 3(C3)降低,内皮下增生和渗出性 GN 发展为膜增生性肾小球肾炎(MPGN);此外,C3 为主或共同主导的肾小球免疫荧光染色是诊断 IRGN 的核心。此外,最初从 A 组细胞质部分分离出来的肾炎相关纤溶酶受体(NAPlr)作为 C3 为主的肾小球损伤的重要诱导剂,是 IRGN 的关键诊断生物标志物。同时,由于补体替代途径(AP)获得性或遗传性失调而表现出 MPGN 组织学模式的“C3 肾小球病(C3G)”,也类似于 C3 为主的 IRGN。最初,C3G 的特征是肾小球上密集的“孤立 C3”沉积。然而,更新的定义允许在 C3 阳性占主导地位且至少比任何其他免疫反应物高出两个数量级的情况下,在肾小球沉积其他补体因子或免疫球蛋白,如果存在 C3 阳性,这使得快速区分 IRGN 和 C3G 的病理形态学发现变得具有挑战性。至于 NAPlr,它被证明可以在体外直接诱导补体 AP 激活,并且在 IRGN 的发展中加重肾小球损伤。最近的一份报告表明,在儿童 PIGN 患者中,抗因子 B 自身抗体是补体 AP 激活的一个促成因素。此外,还报道了没有感染证据但有肾小球 NAPlr 沉积的 C3G。综上所述,IRGN 的临床病理特征与 C3G 有很大的重叠。在这篇综述中,强调了这两种疾病的相似之处和不同之处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18aa/10179079/6b5e314541cd/ijms-24-08432-g001.jpg

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