自身抗体
尼福林
肾病综合征
医学
免疫荧光
抗体
免疫学
共域化
膜性肾病
生物标志物
重组DNA
离体
微小变化病
肾病
队列
肾小球肾炎
肾脏疾病
免疫染色
疾病
内科学
病理
肾病科
免疫病理学
足细胞
人类疾病
蛋白尿
免疫球蛋白G
单克隆抗体
临床意义
全身性疾病
作者
Francesco Pecoraro,Luca Perico,Federica Casiraghi,Paola Rizzo,Matias Trillini,Andrea Angeletti,Manuel Alfredo Podestà,Xhuliana Kajana,Agnese Spennacchio,Marta Todeschini,Marilena Mister,Giuseppe Castellano,Ariela Benigni,Giuseppe Remuzzi
摘要
BACKGROUND: Anti-nephrin autoantibodies have emerged as a putative pathogenic driver in a subset of patients with podocytopathies, including those with post-transplant disease recurrence. METHODS: We measured anti-nephrin autoantibodies in a cohort of 65 patients with podocytopathy associated with steroid-sensitive nephrotic syndrome (n = 39) and steroid-resistant nephrotic syndrome (n = 26), and in 34 patients with post-transplant podocytopathy recurrence. Fourteen patients with membranous nephropathy and 20 healthy volunteers served as controls. ELISA and immunoprecipitation assays were performed to detect anti-nephrin IgG using two different recombinant human nephrin proteins. Immunofluorescence analysis was performed to assess the deposition of IgG and their colocalization with nephrin in renal biopsies. RESULTS: When using murine antigen-based ELISA, the highest positivity was found in healthy volunteers (55%), correlating with levels of circulating natural anti-α-galactose-α-1,3-galactose antibodies. This cross-reactivity was abrogated with recombinant human nephrin expressed in human cells. In this setting, very low prevalence (<5%) of anti-nephrin antibody-positive patients was found in steroid-sensitive and steroid-resistant nephrotic syndrome cohorts and in patients with post-transplant disease recurrence. These frequencies were comparable to healthy volunteers. Using confocal and super-resolution microscopy, only trace amounts of IgM, but no IgG, were found in the glomeruli of analyzed biopsies, which did not colocalize with nephrin. CONCLUSIONS: With the methodology presented here, anti-nephrin reactivity was extremely rare and occurred at comparably low frequencies in healthy controls, native-kidney podocytopathies, and post-transplant disease recurrence. This suggests that these autoantibodies are not inherently disease-specific and may not serve as a broad biomarker across podocytopathies. CLINICALTRIALS: gov NCT06334692. FUNDING: Private donation.
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