H. Yokoyama, M. Shimizu, T. Wada, K. Yoshimoto, Y. Iwata, Kazuaki Shimizu, N. Sakai, K. Furuichi, Y. Hisada, H. Takakuwa, Ken‐ichi Kobayashi
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Two patients with MCNS, 1 with FSGS, and 1 with MN and FSGS showed a dramatic decrease of proteinuria (-30% and -94%) in their urine protein/creatinine ratio. Three out of 4 patients had a complete or partial remission (proteinuria <1g/day) within 8 weeks following immunosuppressive therapy. During the LCAP, T cells, especially activated T cells, decreased significantly in the response group. The other 2 patients, 1 with FSGS and 1 with MN, however, had no response to LCAP and following immunosuppressive therapy or low-density lipoprotein apheresis and suffered from end-stage renal failure or death by pneumonia. 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引用次数: 10
摘要
来自循环T细胞的大量通透性因子(或多个因子)在肾病综合征蛋白尿(NS)中起着至关重要的作用。我们使用Cellsorba (Asahi Medical Co., Osaka, Japan)对6例原发性NS患者、2例微小改变肾病综合征(MCNS)患者、2例局灶节段性肾小球硬化(FSGS)患者、1例膜性肾病(MN)患者和1例MN合并FSGS患者进行了淋巴细胞穿刺(LCAP)去除致病性T细胞的尝试。5例患者连续2周进行2次LCAP,随后给予皮质类固醇治疗(含或不含环孢素A)。2例MCNS患者,1例FSGS患者,1例MN和FSGS患者尿蛋白/肌酐比值显著降低(-30%和-94%)。4例患者中有3例在免疫抑制治疗后8周内完全或部分缓解(蛋白尿<1g/天)。在LCAP期间,反应组的T细胞,尤其是活化T细胞明显减少。然而,另外2例患者,1例FSGS和1例MN,对LCAP没有反应,在免疫抑制治疗或低密度脂蛋白分离后,出现终末期肾功能衰竭或死于肺炎。这些结果表明,LCAP可能对NS,特别是MCNS和一些FSGS患者的治疗有有益的作用,尽管LCAP和伴随的免疫抑制治疗的反应不同。
The beneficial effects of lymphocytapheresis for treatment of nephrotic syndrome.
A considerable permeability factor (or factors) derived from circulating T cells has a crucial role in proteinuria of nephrotic syndrome (NS). We attempted to remove pathogenic T cells through lymphocytapheresis (LCAP) in 6 patients with primary NS, 2 patients with minimal change nephrotic syndrome (MCNS), 2 patients with focal segmental glomerulosclerosis (FSGS), 1 patient with membranous nephropathy (MN), and 1 patient with MN and FSGS using Cellsorba (Asahi Medical Co., Osaka, Japan). LCAP was performed 2 times in 2 consecutive weeks and was followed with corticosteroid therapy with or without cyclosporine A in 5 patients. Two patients with MCNS, 1 with FSGS, and 1 with MN and FSGS showed a dramatic decrease of proteinuria (-30% and -94%) in their urine protein/creatinine ratio. Three out of 4 patients had a complete or partial remission (proteinuria <1g/day) within 8 weeks following immunosuppressive therapy. During the LCAP, T cells, especially activated T cells, decreased significantly in the response group. The other 2 patients, 1 with FSGS and 1 with MN, however, had no response to LCAP and following immunosuppressive therapy or low-density lipoprotein apheresis and suffered from end-stage renal failure or death by pneumonia. These results suggested that LCAP might have a beneficial effect on the treatment of NS, especially MCNS and in some patients with FSGS, despite varying responses to LCAP and concomitant immunosuppressive therapy.