PLA2R染色对儿科膜性肾病的诊断和治疗有重要意义

Hiroshi Tamura, Keishiro Furuie, S. Kuraoka, T. Kawano, H. Nakazato
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摘要

特发性膜性肾病(IMN)是一种罕见的儿童疾病。在患有肾病综合征的儿童中发病率为1.5%。一些研究也调查了m型磷脂酶A2受体(PLA2R)在儿科IMN中的潜在作用,报道了儿童肾脏的低阳性率。因此,我们使用抗pla2r抗体对8例小儿IMN患者的肾活检标本进行免疫荧光染色。我们利用IMN患儿的组织研究了PLA2R的肾小球表达,并在PubMed上检索了关于小儿IMN中PLA2R染色的论文。本研究及其他三项研究中诊断为IMN患者的临床特征:共20例儿童(2-12岁;平均年龄7.4±2.8岁,青少年25例(13-19岁;平均年龄15.9±2.0岁,男性25例(55.6%),女性20例(44.4%),其中23例(51.1%)IMN患者pla2r阳性。此外,我们通过在线搜索找到了三篇论文。在患有IMN的儿童中,PLA2R的表达大约有一半是阳性的,因此研究儿童PLA2R的致病抗原是有用的。抗pla2r抗体表达强度反映了本研究患者的疾病活动性(尿蛋白水平)。参考PLA2R的表达强度,可以在免疫抑制治疗中调整药物剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PLA2R Staining is Useful for the Diagnosis and Treatment of Membranous Nephropathy in Pediatric Patients
Idiopathic membranous nephropathy (IMN) is a rare disease in children. The incidence is 1.5% in children with nephrotic syndrome. A few studies have also investigated the M-type phospholipase A2 receptor’s (PLA2R) potential role in pediatric IMN, reporting a low positive rate in pediatric kidneys. Therefore, we conducted immunofluorescence staining using an anti-PLA2R antibody in the renal biopsy specimens of eight pediatric patients with IMN. We studied the glomerular expression of PLA2R using tissues from children with IMN, and searched for papers on PLA2R staining in pediatric IMN on PubMed. Clinical characteristics of patients diagnosed with IMN in this study and the other three studies: A total of 20 pediatric (aged 2–12 years; mean age 7.4 ± 2.8 years) patients and 25 adolescent (aged 13–19 years; mean age 15.9 ± 2.0 years) patients, comprising 25 male (55.6%) and 20 female (44.4%) patients, with 23 (51.1%) patients with IMN being PLA2R-positive, were found to be eligible for this study. Furthermore, we found three papers through our online search. PLA2R expression can be approximately half positive in children with IMN, and it is useful to investigate the causative antigen of PLA2R in children. The intensity of anti-PLA2R antibody expression reflected the disease activity (urinary protein level) of the patients in this study. It is possible to adjust the drug dose in immunosuppressive therapy with reference to the expression intensity of PLA2R.
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