Renal Unit, Alexandra Hospital Department of Pathology, Medical School, University of Athens, Athens, Greece.
Artif Organs. 2011 Apr;35(4):420-5. doi: 10.1111/j.1525-1594.2010.01068.x.
Therapy for recurrent focal segmental glomerulosclerosis (FSGS) in the renal allograft is largely based on case reports. The use of plasmapheresis alone (based on its effectiveness in children) appears less effective in adults, reaching a response rate of <40%. Recently, rituximab, an anti-CD20 monoclonal chimeric antibody, showed promising results as rescue therapy in plasmapheresis-resistant recurrent FSGS. However, following rituximab administration, response is variable, often slow and consequently overlooked. We report a series of four cases of recurrent FSGS following renal transplantation successfully treated with a combination of plasmapheresis and rituximab. Complete remission of proteinuria occurred in two and partial remission in the other two patients whereas renal function improved or remained stable. During treatment and the follow-up period (18-60 months) no severe infectious complications were observed. Our data suggest that the combination of plasmapheresis and rituximab is an acceptable treatment in patients with post-transplantation recurrent FSGS.
在肾移植中,复发性局灶节段性肾小球硬化(FSGS)的治疗主要基于病例报告。单独使用血浆置换(基于其在儿童中的有效性)在成人中效果较差,反应率<40%。最近,利妥昔单抗,一种抗 CD20 单克隆嵌合抗体,作为血浆置换抵抗性复发性 FSGS 的挽救治疗显示出有前途的结果。然而,在利妥昔单抗给药后,反应是可变的,通常缓慢,因此容易被忽视。我们报告了 4 例肾移植后复发性 FSGS 成功治疗的病例,采用血浆置换和利妥昔单抗联合治疗。2 例患者蛋白尿完全缓解,2 例患者部分缓解,而肾功能改善或保持稳定。在治疗和随访期间(18-60 个月)未观察到严重感染并发症。我们的数据表明,血浆置换和利妥昔单抗联合治疗是移植后复发性 FSGS 患者可接受的治疗方法。