Division of Nephrology, The Hospital for Sick Children, University of Toronto, ON, Canada.
Am J Transplant. 2012 Sep;12(9):2546-53. doi: 10.1111/j.1600-6143.2012.04124.x. Epub 2012 Jun 8.
Antibody mediated rejection (AMR) activates the classical complement pathway and can be detrimental to graft survival. AMR can be accompanied by thrombotic microangiopathy (TMA). Eculizumab, a monoclonal C5 antibody prevents induction of the terminal complement cascade (TCC) and has recently emerged as a therapeutic option for AMR. We present a highly sensitized 13-year-old female with end-stage kidney disease secondary to spina bifida-associated reflux nephropathy, who developed severe steroid-, ATG- and plasmapheresis-resistant AMR with TMA 1 week post second kidney transplant despite previous desensitization therapy with immunoglobulin infusions. Eculizumab rescue therapy resulted in a dramatic improvement in biochemical (C3; creatinine) and hematological (platelets) parameters within 6 days. The patient was proven to be deficient in complement Factor H-related protein 3/1 (CFHR3/1), a plasma protein that regulates the complement cascade at the level of C5 conversion and has been involved in the pathogenesis of atypical hemolytic uremic syndrome caused by CFH autoantibodies (DEAP-HUS). CFHR1 deficiency may have worsened the severe clinical progression of AMR and possibly contributed to the development of donor-specific antibodies. Thus, screening for CFHR3/1 deficiency should be considered in patients with severe AMR associated with TMA.
抗体介导的排斥反应 (AMR) 会激活经典补体途径,从而对移植物的存活造成损害。AMR 可伴有血栓性微血管病 (TMA)。Eculizumab 是一种单克隆 C5 抗体,可防止末端补体级联反应 (TCC) 的诱导,最近已成为 AMR 的治疗选择。我们报告了一例高度致敏的 13 岁女性,因脊柱裂相关反流性肾病导致终末期肾病,在第二次肾移植后 1 周发生严重的激素、ATG 和血浆置换抵抗性 AMR 伴 TMA,尽管之前已进行免疫球蛋白输注脱敏治疗。Eculizumab 抢救治疗在 6 天内显著改善了生化(C3;肌酐)和血液学(血小板)参数。该患者被证明缺乏补体因子 H 相关蛋白 3/1(CFHR3/1),这是一种调节 C5 转化水平补体级联反应的血浆蛋白,与 CFH 自身抗体引起的非典型溶血尿毒症综合征(DEAP-HUS)的发病机制有关。CFHR1 缺乏可能使 AMR 的严重临床进展恶化,并可能导致供体特异性抗体的产生。因此,在伴有 TMA 的严重 AMR 患者中,应考虑筛查 CFHR3/1 缺乏症。