肾移植后复发性膜性肾病的补体受体 1 增强:病例报告

IF 3.2 Q1 UROLOGY & NEPHROLOGY
Noriyuki Kounoue , Hideyo Oguchi , Akinori Hashiguchi , Kazuho Honda , Dedong Kang , Tetuo Mikami , Naobumi Tochigi , Takeshi Kawamura , Yoshihiro Itabashi , Takashi Yonekura , Kei Sakurabayashi , Ken Sakai
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引用次数: 0

摘要

膜性肾病(MN)会在一些肾脏异体移植患者身上复发,而且复发会增加移植失败率。我们介绍了一例在第一和第二次异体移植中复发的 MN,其肾小球毛细血管壁补体受体 1(CR1)阳性与免疫球蛋白 G(IgG)一致。一名 20 多岁的男子出现了 MN,并开始进行血液透析。第一次移植后,MN 复发并导致移植物损失,第二次移植后不久再次复发。IgG亚类染色几乎一致为阴性,IgG4和磷脂酶A2受体(PLA2R)染色均为阴性。考虑为病因不明的复发性 MN。质谱分析表明,移植肾活检组织中的 CR1 增高。免疫组化和免疫荧光研究表明,在该病例中,CR1与IgG沿肾小球毛细血管共聚焦,而在PLA2R相关MN的对照病例中,CR1定位于荚膜细胞,IgG没有共聚焦。相关的光镜和免疫电镜检查显示,CR1 定位于电子致密沉积物和荚膜细胞之间的界面。总之,该病例显示了 CR1 独特的增强和定位。迄今为止,CR1 增强的 MN 病例尚未见报道。CR1 可能是本例复发性 MN 的候选致病抗原,但仍需进一步研究 CR1 的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complement Receptor 1 Enhancement in Recurrent Membranous Nephropathy Following Kidney Transplantation: A Case Report

Membranous nephropathy (MN) recurs in some kidney allograft patients, and recurrence increases graft failure rates. We present a unique case of recurrent MN in first and second allografts showing glomerular capillary wall-positivity for complement receptor 1 (CR1) consistent with immunoglobulin G (IgG). A man in his late 20s developed MN and started hemodialysis. MN recurred and caused graft loss after the first transplantation and recurred again soon after the second transplantation. The IgG subclass staining was almost consistently negative for IgG4 and phospholipase A2 receptor (PLA2R)-staining was negative. Recurrent MN of unknown etiology was considered. Mass spectrometry demonstrated that CR1 had increased in the transplanted kidney biopsies. Immunohistochemistry and immunofluorescence studies demonstrated CR1 colocalized with IgG along glomerular capillaries in this case, whereas CR1 was localized in podocytes with no colocalization of IgG in a control case of PLA2R-associated MN. Correlative light and immunoelectron microscopy showed localization of CR1 at the interface between electron-dense deposits and podocytes. Collectively, this case demonstrated a unique enhancement and localization of CR1. MN with enhancement of CR1 has not been reported to date. CR1 may be a candidate causative antigen in this case of recurrent MN, although further study is needed to investigate the pathogenesis of CR1.

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来源期刊
Kidney Medicine
Kidney Medicine Medicine-Internal Medicine
CiteScore
4.80
自引率
5.10%
发文量
176
审稿时长
12 weeks
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