Beck Laurence H, Bonegio Ramon G B, Lambeau Gérard, Beck David M, Powell David W, Cummins Timothy D, Klein Jon B, Salant David J
Boston University School of Medicine, Boston, MA, USA.
N Engl J Med. 2009 Jul 2;361(1):11-21. doi: 10.1056/NEJMoa0810457.
Idiopathic membranous nephropathy, a common form of the nephrotic syndrome, is an antibody-mediated autoimmune glomerular disease. Serologic diagnosis has been elusive because the target antigen is unknown.
We performed Western blotting of protein extracts from normal human glomeruli with serum samples from patients with idiopathic or secondary membranous nephropathy or other proteinuric or autoimmune diseases and from normal controls. We used mass spectrometry to analyze the reactive protein bands and confirmed the identity and location of the target antigen with a monospecific antibody.
Serum samples from 26 of 37 patients (70%) with idiopathic but not secondary membranous nephropathy specifically identified a 185-kD glycoprotein in nonreduced glomerular extract. Mass spectrometry of the reactive protein band detected the M-type phospholipase A(2) receptor (PLA(2)R). Reactive serum specimens recognized recombinant PLA(2)R and bound the same 185-kD glomerular protein as did the monospecific anti-PLA(2)R antibody. Anti-PLA(2)R autoantibodies in serum samples from patients with membranous nephropathy were mainly IgG4, the predominant immunoglobulin subclass in glomerular deposits. PLA(2)R was expressed in podocytes in normal human glomeruli and colocalized with IgG4 in immune deposits in glomeruli of patients with membranous nephropathy. IgG eluted from such deposits in patients with idiopathic membranous nephropathy, but not in those with lupus membranous or IgA nephropathy, recognized PLA(2)R.
A majority of patients with idiopathic membranous nephropathy have antibodies against a conformation-dependent epitope in PLA(2)R. PLA(2)R is present in normal podocytes and in immune deposits in patients with idiopathic membranous nephropathy, indicating that PLA(2)R is a major antigen in this disease.
特发性膜性肾病是肾病综合征的一种常见形式,是一种抗体介导的自身免疫性肾小球疾病。由于靶抗原未知,血清学诊断一直难以实现。
我们用来自特发性或继发性膜性肾病患者、其他蛋白尿或自身免疫性疾病患者以及正常对照的血清样本,对正常人肾小球的蛋白质提取物进行蛋白质印迹分析。我们使用质谱分析反应性蛋白条带,并用单特异性抗体确认靶抗原的身份和定位。
37例特发性而非继发性膜性肾病患者中的26例(70%)的血清样本在非还原肾小球提取物中特异性识别出一种185-kD糖蛋白。对反应性蛋白条带进行质谱分析检测到M型磷脂酶A2受体(PLA2R)。反应性血清标本识别重组PLA2R,并与单特异性抗PLA2R抗体结合相同的185-kD肾小球蛋白。膜性肾病患者血清样本中的抗PLA2R自身抗体主要为IgG4,是肾小球沉积物中的主要免疫球蛋白亚类。PLA2R在正常人肾小球的足细胞中表达,并与膜性肾病患者肾小球免疫沉积物中的IgG4共定位。从特发性膜性肾病患者而非狼疮性膜性或IgA肾病患者的此类沉积物中洗脱的IgG识别PLA2R。
大多数特发性膜性肾病患者具有针对PLA2R中构象依赖性表位的抗体。PLA2R存在于正常足细胞和特发性膜性肾病患者的免疫沉积物中,表明PLA2R是该疾病的主要抗原。