İDİOPATİK MEMBRANÖZ NEFROPATİDE TEDAVİ ÖNCESİ SERUM KOMLEMAN 3 SEVİYESİ VE RİTUKSİMAB YANITI

Engin ONAN, Dilek TORUN, Rüya ÖZELSANCAK, Hasan MİCOZKADIOĞLU
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Abstract

Objective: The efficacy of rituximab has been reported in patients with idiopathic membranous nephropathy (MN). We aimed to evaluate the relationship between biochemical tests at diagnosis, immunohistochemical profile, and rituximab response in patients with idiopathic MN unresponsive to other therapies in our center. Material and Methods: In this study, nine patients with idiopathic MN who received other immunosuppressive therapies between 2017-2022 and who underwent renal biopsy in our center were evaluated. Pre-treatment phospholipase A2 antibody levels were positive in 6 patients, and antibodies could not be analyzed in 3 patients. All patients received rituximab ≥2 grams after renin-angiotensin-aldosterone system (RAAS) blocker, cyclophosphamide, steroid, and calcineurin inhibitors. Results: Of the nine patients included in the study, 7 (78.2%) were male, and the mean age was 39.713.2 years. Four patients had complete remission (CR) with rituximab treatment, and five had partial remission (PR). Sclerotic glomeruli count, IgG, A, M, C1q, C3, C4d, fibrinogen, kappa and lambda staining, tubular atrophy, and interstitial fibrosis findings on renal biopsy were similar. However, the serum complement 3 (C3) level was significantly lower within normal limits (1.22  0.26 vs 1.560  0.56 p=0.016). The mean arterial pressure was significantly higher (96.22.5 mmHg vs 84.754.27 mmHg, p=0.018) in patients with partial remission compared to those with complete remission. Conclusion: A low baseline serum C3 level within normal limits before treatment in patients with idiopathic membranous nephropathy may help predicting unresponsiveness to other immunosuppressive therapies and partial response to rituximab treatment.
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特发性膜性肾病患者治疗前血清补体 3 水平和对利库西单抗的反应
目的:报道了利妥昔单抗治疗特发性膜性肾病(MN)的疗效。我们的目的是评估在我们中心对其他治疗无反应的特发性MN患者的诊断生化试验、免疫组织化学谱和利妥昔单抗反应之间的关系。材料和方法:在本研究中,对2017-2022年期间接受其他免疫抑制治疗并在本中心进行肾活检的9例特发性MN患者进行评估。6例患者治疗前磷脂酶A2抗体水平为阳性,3例患者抗体无法分析。所有患者在肾素-血管紧张素-醛固酮系统(RAAS)阻滞剂、环磷酰胺、类固醇和钙调磷酸酶抑制剂后接受利妥昔单抗治疗≥2g。结果:纳入研究的9例患者中,男性7例(78.2%),平均年龄39.713.2岁。通过利妥昔单抗治疗,4例患者完全缓解(CR), 5例部分缓解(PR)。硬化肾小球计数、IgG、A、M、C1q、C3、C4d、纤维蛋白原、kappa和lambda染色、肾活检小管萎缩和间质纤维化的结果相似。然而,血清补体3 (C3)水平明显低于正常范围(1.220.26 vs 1.5600.56 p=0.016)。部分缓解患者的平均动脉压明显高于完全缓解患者(96.22.5 mmHg vs 84.754.27 mmHg, p=0.018)。结论:特发性膜性肾病患者治疗前在正常范围内的低基线血清C3水平可能有助于预测对其他免疫抑制疗法的无反应性和对利妥昔单抗治疗的部分反应。
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