Kidney After Nonrenal Transplantation-The Impact of Alemtuzumab Induction

被引:10
|
作者
Shapiro, Ron [1 ]
Basu, Amit
Tan, Henkie P.
Morgan, Claire
Sharma, Vivek
Blisard, Deanna
Randhawa, Parmjeet S. [2 ]
Dvorchik, Igor
McCauley, Jerry
Ellis, Demetrius [3 ]
Marsh, J. Wallis
Webber, Steven [4 ]
Kurland, Geoffrey [5 ]
McCurry, Kenneth R. [6 ]
Abu-Elmagd, Kareem
Mazariegos, George
Starzl, Thomas E.
机构
[1] Univ Pittsburgh, Med Ctr, Thomas E Starzl Transplantat Inst, Div Transplantat,Dept Surg, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Pathol, Thomas E Starzl Transplantat Inst, Pittsburgh, PA 15213 USA
[3] Childrens Hosp Pittsburgh, Div Nephrol, Pittsburgh, PA 15213 USA
[4] Childrens Hosp Pittsburgh, Div Cardiol, Pittsburgh, PA 15213 USA
[5] Childrens Hosp Pittsburgh, Div Pulmonol, Pittsburgh, PA 15213 USA
[6] Univ Pittsburgh, Div Cardiothorac Transplantat, Pittsburgh, PA 15213 USA
关键词
Kidney; Nonrenal; Alemtuzumab; TACROLIMUS MONOTHERAPY; RENAL-TRANSPLANTATION; IMMUNOSUPPRESSION; TOLERANCE;
D O I
10.1097/TP.0b013e3181b4aaf5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. 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. Patients and Methods. 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. Results. 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. Conclusion. Alemtuzumab induction with simple resumption of baseline immunosuppression in patients undergoing kidney transplantation after nonrenal transplantation represents a reasonable immunosuppressive strategy.
引用
收藏
页码:799 / 802
页数:4
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