Shapiro Ron, Basu Amit, Tan Henkie P, Morgan Claire, Sharma Vivek, Blisard Deanna, Randhawa Parmjeet S, Dvorchik Igor, McCauley Jerry, Ellis Demetrius, Marsh J Wallis, Webber Steven, Kurland Geoffrey, McCurry Kenneth R, Abu-Elmagd Kareem, Mazariegos George, Starzl Thomas E
Department of Surgery, Division of Transplantation, Thomas E. Starzl Transplantation Institute, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Transplantation. 2009 Sep 27;88(6):799-802. doi: 10.1097/TP.0b013e3181b4aaf5.
Calcineurin inhibitor nephrotoxicity in nonrenal allograft recipients can lead to end-stage renal disease and the need for kidney transplantation. We sought to evaluate the role of alemtuzumab induction in this population.
We evaluated 144 patients undergoing kidney transplantation after nonrenal transplantation between May 18, 1998, and October 8, 2007. Seventy-two patients transplanted between January 15, 2003, and October 8, 2007, received alemtuzumab induction and continued their pretransplant immunosuppression. Seventy-two patients transplanted between May 18, 1998, and July 21, 2007, did not receive alemtuzumab induction, but received additional steroids and maintenance immunosuppression. Donor and recipient demographics were comparable.
Overall, 1- and 3-year patient survival and renal function were comparable between the two groups. One- and 3-year graft survival was 93.0% and 75.3% in the alemtuzumab group and 83.3% and 68.7% in the no alemtuzumab group, respectively (P=0.051). The incidence of acute rejection was lower in the alemtuzumab group, 15.3%, than in the no alemtuzumab group, 41.7% (P=0.0001). The incidence of delayed graft function was lower in the alemtuzumab group, 9.7%, than in the no alemtuzumab group, 25.0% (P=0.003). The incidence of viral complications was comparable.
Alemtuzumab induction with simple resumption of baseline immunosuppression in patients undergoing kidney transplantation after nonrenal transplantation represents a reasonable immunosuppressive strategy.
非肾移植受者中钙调神经磷酸酶抑制剂肾毒性可导致终末期肾病,并需要进行肾移植。我们试图评估阿仑单抗诱导在该人群中的作用。
我们评估了1998年5月18日至2007年10月8日期间接受非肾移植后进行肾移植的144例患者。2003年1月15日至2007年10月8日期间接受移植的72例患者接受了阿仑单抗诱导,并继续其移植前免疫抑制治疗。1998年5月18日至2007年7月21日期间接受移植的72例患者未接受阿仑单抗诱导,但接受了额外的类固醇和维持免疫抑制治疗。供体和受体的人口统计学特征具有可比性。
总体而言,两组患者1年和3年的生存率及肾功能相当。阿仑单抗组1年和3年的移植物生存率分别为93.0%和75.3%,未使用阿仑单抗组分别为83.3%和68.7%(P=0.051)。阿仑单抗组急性排斥反应的发生率较低,为15.3%,低于未使用阿仑单抗组的41.7%(P=0.0001)。阿仑单抗组移植肾功能延迟的发生率较低,为9.7%,低于未使用阿仑单抗组的25.0%(P=0.003)。病毒并发症的发生率相当。
对于非肾移植后接受肾移植的患者,采用阿仑单抗诱导并简单恢复基线免疫抑制是一种合理的免疫抑制策略。