Schulz T, Flecken M, Kapischke M, Busing M
Department of Surgery, Ruhr-University, Bochum, Germany.
Transplant Proc. 2005 May;37(4):1818-20. doi: 10.1016/j.transproceed.2005.02.087.
Since 1996, preoperative single-shot dose antithymocyte globuline (ATG) with prednisolone (PRD), mycophenolate mofetile (MMF), and tacrolimus (TAC) is the favorite induction therapy in our center. In a series of 25 first simultaneous pancreas and kidney transplant (SPK) recipients, 5 doses of daclizumab were administered in addition to standard induction. Here we present our 3-year experience. Immunosuppression was started prior to reperfusion consisting of daclizumab (1 mg/kg body weight [bw]), ATG (4-6 mg/kg bw) and 250 mg PRD. After surgery, PRD was reduced gradually, TAC trough levels were between 8-15 ng/mL, MMF was given twice daily (2-3 g/d) as well as 4 further doses dacilzumab every 14 days. After 3 years, patient, pancreas, and kidney graft survival rates are 100%, 84%, and 92%, respectively. Four pancreas grafts were lost (chronic allograft dysfunction, n = 2; recurrent abdominal infection, n = 1; acute rejection [AR] without treatment, n = 1). Both patients suffering from severe infection and untreated AR lost their kidney graft too. During the first 3 months after SPK, 3 AR episodes were observed in 2 patients (8%). After a 3-year period, 8 AR episodes occurred in 7 recipients (28%). AR was treated using PRD (n = 5) or ATG (n = 1). In 1 case, immunosuppression was switched from TAC to sirolimus successfully. Overall, 8 AR episodes occurred in 7 patients (28%) during the first 3 years after SPK. One severe infection led to graft lost 13 months after SPK. In this series, the combination of ATG and daclizumab prevented AR episodes, successfully providing considerable 3-year survival rates.
自1996年以来,术前单次剂量抗胸腺细胞球蛋白(ATG)联合泼尼松龙(PRD)、霉酚酸酯(MMF)和他克莫司(TAC)一直是我们中心最常用的诱导治疗方案。在一系列25例首次同期胰腺和肾脏移植(SPK)受者中,除标准诱导治疗外,还给予了5剂达利珠单抗。在此,我们介绍我们的3年经验。免疫抑制在再灌注前开始,包括达利珠单抗(1mg/kg体重[bw])、ATG(4 - 6mg/kg bw)和250mg PRD。术后,PRD逐渐减量,TAC谷浓度维持在8 - 15ng/mL,MMF每日两次给药(2 - 3g/d),并每14天给予4剂达利珠单抗。3年后,患者、胰腺和肾脏移植物存活率分别为100%、84%和92%。4个胰腺移植物丢失(慢性移植物功能障碍,n = 2;反复腹部感染,n = 1;未治疗的急性排斥反应[AR],n = 1)。两名患有严重感染和未治疗AR的患者也失去了他们的肾脏移植物。在SPK后的前3个月,2例患者(8%)发生了3次AR发作。3年后,7例受者(28%)发生了8次AR发作。AR采用PRD(n = 5)或ATG(n = 1)治疗。1例患者成功将免疫抑制从TAC转换为西罗莫司。总体而言,在SPK后的前3年,7例患者(28%)发生了8次AR发作。1例严重感染导致SPK后13个月移植物丢失。在本系列中,ATG和达利珠单抗的联合使用预防了AR发作,成功提供了相当高的3年存活率。