Ayalon Rivka, Beck Laurence H
Department of Medicine, Renal Section, Boston University School of Medicine, 650 Albany Street Boston, Boston, MA, 02118, USA.
Pediatr Nephrol. 2015 Jan;30(1):31-9. doi: 10.1007/s00467-013-2717-z. Epub 2013 Dec 29.
Membranous nephropathy (MN) is an immune complex-mediated cause of the nephrotic syndrome that can occur in all age groups, from infants to the elderly. While systemic disorders such as hepatitis B infection or lupus may more frequently cause secondary MN in the younger population, primary or "idiopathic" MN has generally been considered a disease of adults. Recent progress in our understanding of primary disease was recently made when the target antigen in primary MN was identified as the M-type phospholipase A2 receptor (PLA2R). Circulating anti-PLA2R antibodies may serve both as a diagnostic tool for distinguishing primary from secondary disease and as a biomarker for monitoring the immunologic activity of this organ-specific autoimmune disease during treatment. Whereas definitive therapy for secondary forms of MN should be targeted at the underlying cause, immunosuppressive therapy is often necessary for primary disease. Alkylating agents in combination with corticosteroids, as well as calcineurin inhibitors (± steroids), are first line agents due to randomized controlled trials in an adult population with relatively long durations of follow-up. However, rituximab, mycophenolate and adrenocorticotropic hormone have shown promise in smaller and/or observational studies. The optimal therapy for children and adolescents with MN is less well defined.
膜性肾病(MN)是一种由免疫复合物介导的肾病综合征病因,可发生于从婴儿到老年人的所有年龄组。虽然诸如乙型肝炎感染或狼疮等全身性疾病在较年轻人群中更常导致继发性MN,但原发性或“特发性”MN通常被认为是一种成人疾病。当原发性MN中的靶抗原被确定为M型磷脂酶A2受体(PLA2R)时,我们对原发性疾病的认识最近取得了进展。循环抗PLA2R抗体既可以作为区分原发性疾病和继发性疾病的诊断工具,也可以作为监测这种器官特异性自身免疫性疾病治疗期间免疫活性的生物标志物。虽然继发性MN的确定性治疗应针对潜在病因,但原发性疾病通常需要免疫抑制治疗。由于在随访时间相对较长的成年人群中进行了随机对照试验,烷化剂联合皮质类固醇以及钙调神经磷酸酶抑制剂(±类固醇)是一线治疗药物。然而,利妥昔单抗、霉酚酸酯和促肾上腺皮质激素在规模较小和/或观察性研究中显示出了前景。MN患儿和青少年的最佳治疗方法尚不太明确。