Schulz T, Kapischke M, Busing M
Department of Surgery, Ruhr-University, Bochum, Germany.
Transplant Proc. 2005 May;37(4):1815-7. doi: 10.1016/j.transproceed.2005.02.072.
Ten years ago therapy with antithymocyte globulin or OKT3, azathioprine, cyclosporine, and prednisolone was the most common induction treatment for simultaneous pancreas/ kidney (SPK) recipients. Although immunosuppression was started after surgery, there was a high incidence of acute rejection episodes. In 1995, we modified the application of antithymocyte globulin and prednisolone by starting prior to reperfusion. Between 1995 and 1996, 30 patients underwent a first SPK. Prior to reperfusion, antithymocyte globulin (4-6 mg/kg body weight) and 250 mg prednisolone were administered. Intraoperatively, another 250 mg prednisolone were administered as well as intravenous azathroprine 3 mg/kg. After surgery up to 10 doses of antithymocyte globulin were administered and cyclosporine trough levels targeted to 200 to 250 ng/mL. Prednisolone was reduced gradually. After a median period of 8.5 years (range: 7.8-9.5 years) patient, pancreas, and kidney graft survival were 93.3%, 70%, and 76.7%, respectively. Sixteen acute rejection episodes were diagnosed in 11 patients (36.7%), who were treated with prednisolone bolus (n = 4), prednisolone with OKT3 (n = 8), prednisolone with antithymocyte globulin (n = 1), cyclosporine to tacrolimus conversion (n = 2), or plasmapheresis (n = 1). Two recipients died after SPK due to severe infection or carcinoma with functioning grafts. Seven further pancreas grafts were lost. Five kidney losses were observed besides the two recipients who died with functioning grafts. While previous protocols yielded a rejection incidence after SPK between 50% and 80%, we observed 60% of patients with no rejection episode during an 8.5-year median follow-up.
十年前,抗胸腺细胞球蛋白或OKT3、硫唑嘌呤、环孢素和泼尼松龙联合治疗是同期胰肾联合移植(SPK)受者最常用的诱导治疗方法。尽管免疫抑制在手术后开始,但急性排斥反应的发生率很高。1995年,我们通过在再灌注前开始应用抗胸腺细胞球蛋白和泼尼松龙,对其应用方法进行了改良。1995年至1996年间,30例患者接受了首次SPK手术。再灌注前,给予抗胸腺细胞球蛋白(4 - 6mg/kg体重)和250mg泼尼松龙。术中,再给予250mg泼尼松龙以及静脉注射硫唑嘌呤3mg/kg。术后给予多达10剂抗胸腺细胞球蛋白,并将环孢素谷浓度目标设定为200至250ng/mL。泼尼松龙逐渐减量。经过中位时间8.5年(范围:7.8 - 9.5年),患者、胰腺和肾移植的存活率分别为93.3%、70%和76.7%。11例患者(36.7%)诊断出16次急性排斥反应,分别接受了大剂量泼尼松龙治疗(n = 4)、泼尼松龙联合OKT3治疗(n = 8)、泼尼松龙联合抗胸腺细胞球蛋白治疗(n = 1)、环孢素转换为他克莫司治疗(n = 2)或血浆置换治疗(n = 1)。2例SPK受者因严重感染或有功能移植物的癌症死亡。另外有7个胰腺移植物失功。除了2例有功能移植物的死亡受者外,还观察到5例肾移植失功。虽然之前的方案在SPK后排斥反应发生率为50%至80%,但我们观察到在中位8.5年的随访期间,60%的患者未发生排斥反应。