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阿仑单抗诱导治疗及西罗莫司联合霉酚酸酯维持治疗用于无钙调神经磷酸酶抑制剂和无类固醇的肾移植免疫抑制。

Alemtuzumab induction and sirolimus plus mycophenolate mofetil maintenance for CNI and steroid-free kidney transplant immunosuppression.

作者信息

Flechner S M, Friend P J, Brockmann J, Ismail H R, Zilvetti M, Goldfarb D, Modlin C, Mastroianni B, Savas K, Devaney A, Simmonds M, Cook D J

机构信息

Transplant Center, Cleveland Clinic Foundation, Cleveland, Ohio, USA.

出版信息

Am J Transplant. 2005 Dec;5(12):3009-14. doi: 10.1111/j.1600-6143.2005.01123.x.

Abstract

We performed a pilot study in which 22 kidney recipients (14 LD: 8 DCD) were given alemtuzumab induction (30 mg day 0 and 1), steroids (500 mg mp day 0 and 1, none thereafter), mycophenolate mofetil (MMF) maintenance (500 mg b.i.d) and sirolimus (concentration controlled 8-12 ng/mL). With a mean follow-up of 15.9 months, patient survival is (21/22) 96% and graft survival (19/22) 87%. Acute rejections occurred in (8) 36.3% (two humoral). Of 19 surviving grafts, 18 (95%) remain steroid and 15 (79%) CNI-free. At 1 year, mean creatinine was 1.43 mg/dL. Overall infection rates were low, but 2 patients developed severe acute respiratory distress syndrome (ARDS) at month 3 and 7, respectively, resulting in mortality in one and a graft loss in the other. No cancer or PTLD was observed. Leukopenia was common and MMF dose was reduced or eliminated in 6/22 (27%) patients. The reported higher than expected rate of acute rejection, leukopenia and possible pulmonary toxicity suggests excessive morbidity. Modifications such as an initial period of CNI use should be considered.

摘要

我们开展了一项试点研究,对22例肾移植受者(14例活体供肾:8例心死亡后器官捐献)进行阿仑单抗诱导治疗(第0天和第1天各30 mg)、类固醇治疗(第0天和第1天静脉注射500 mg,此后不再使用)、霉酚酸酯维持治疗(500 mg,每日两次)以及西罗莫司治疗(浓度控制在8 - 12 ng/mL)。平均随访15.9个月,患者生存率为(21/22)96%,移植物生存率为(19/22)87%。8例(36.3%)发生急性排斥反应(2例为体液性排斥)。在19个存活的移植物中,18个(95%)不再使用类固醇,15个(79%)不再使用钙调神经磷酸酶抑制剂。1年时,平均肌酐水平为1.43 mg/dL。总体感染率较低,但分别有2例患者在第3个月和第7个月发生严重急性呼吸窘迫综合征(ARDS),其中1例死亡,另1例移植物丢失。未观察到癌症或移植后淋巴细胞增生性疾病(PTLD)。白细胞减少很常见,22例患者中有6例(27%)减少或停用了霉酚酸酯剂量。所报告的急性排斥反应、白细胞减少和可能的肺部毒性发生率高于预期,提示发病率过高。应考虑进行一些调整,如初始阶段使用钙调神经磷酸酶抑制剂。

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