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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Alemtuzumab induction and tacrolimus monotherapy in pancreas transplantation: One- and two-year outcomes.
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Alemtuzumab induction and tacrolimus monotherapy in pancreas transplantation: One- and two-year outcomes.

机译:胰腺移植中使用Alemtuzumab诱导和他克莫司单药治疗:一年和两年的结果。

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BACKGROUND: Alemtuzumab (Campath-1H) induction with tacrolimus monotherapy has been shown to provide effective immunosuppression for kidney, liver, lung, and small bowel transplantation. This drug combination was evaluated in pancreas transplant recipients. METHODS: Sixty consecutive pancreas transplants (30 simultaneous pancreas-kidney, 20 pancreas after kidney, and 10 pancreas alone) were carried out under this protocol between July 2003 to January 2005. The mean follow-up was 22 months (range 17-33). RESULTS: One-year patient, pancreas, and kidney allograft survival were 95%, 93%, and 90%, respectively. With 22 months follow-up, patient, pancreas, and kidney survival were 94%, 89%, and 87%, respectively. The rejection rate was 30% (18/60), with four patients (7%) experiencing steroid-resistant rejection. Major infection occurred in three (5%) patients resulting in two (3.3%) deaths from disseminated histoplasmosis and a herpes virus infection. One patient with cryptococcal meningitis was successfully treated. Seven (11.7%) patients experienced cytomegalovirus infection, all of whom responded to treatment with ganciclovir. One (1.7%) case of polymorphic posttransplant lymphoproliferative disease was seen, which regressed with a temporary discontinuation of tacrolimus and high-dose ganciclovir. The mean serum creatinine of the 30 simultaneous pancreas-kidney transplants at one year posttransplant was 1.37+/-0.33 mg/ml. The preexisting creatinine in pancreas after kidney transplants was not adversely affected by this immunosuppressive protocol. CONCLUSION: A single dose of perioperative alemtuzumab followed by daily tacrolimus monotherapy provides effective immunosuppression for pancreas transplantation, but the optimal use of this drug combination is not yet clear.
机译:背景:他克莫司单药诱导Alemtuzumab(Campath-1H)可以为肾,肝,肺和小肠移植提供有效的免疫抑制。在胰腺移植受者中评估了这种药物组合。方法:根据该方案,在2003年7月至2005年1月间进行了60例连续胰腺移植(同时行30例胰肾,20例肾脏肾移植和10例胰腺移植)。平均随访时间为22个月(范围17-33)。 。结果:一年患者,胰腺和肾同种异体移植存活率分别为95%,93%和90%。经过22个月的随访,患者,胰腺和肾脏的存活率分别为94%,89%和87%。排斥率为30%(18/60),其中四名患者(7%)经历类固醇耐药性排斥。三例(5%)患者发生了严重感染,导致弥漫性组织胞浆菌病和疱疹病毒感染导致两人(3.3%)死亡。一名隐球菌性脑膜炎患者获得成功治疗。七名(11.7%)患者经历了巨细胞病毒感染,所有患者均接受更昔洛韦治疗。观察到一例(1.7%)多态性移植后淋巴组织增生性疾病,其随着他克莫司和大剂量更昔洛韦的暂时停药而消退。移植后一年中同时进行的30例胰腺-肾脏移植的平均血清肌酐为1.37 +/- 0.33 mg / ml。肾脏移植后胰腺中预先存在的肌酐不受这种免疫抑制方案的不利影响。结论:围手术期单剂量阿仑单抗随后每日他克莫司单药治疗可为胰腺移植提供有效的免疫抑制作用,但该药物组合的最佳使用尚不清楚。

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