Conley S B, al-Uzri A, So S, Salvatierra O
Department of Pediatrics, California Pacific Medical Center, San Francisco 94115.
Transplantation. 1994 Feb 27;57(4):540-4.
During the two-year period May 1991 to April 1993, 36 kidney transplants were performed in children less than 18 years of age at California Pacific Medical Center using an aggressive quadruple-therapy regimen of immunosuppression. The regimen consisted of induction with an antilymphocyte preparation (MALG in 21, OKT3 in 2, ATGAM in 12, none in 1), initial moderate-dose steroid therapy, early intravenous cyclosporine therapy, and azathioprine. Twenty living-related graft recipients were pretreated with donor-specific transfusions. Long-term cyclosporine was dosed by levels to keep through whole-blood levels (RIA) at 200-300 ng/ml. Twenty-five grafts were from living-related donors, two from living unrelated donors, and nine from cadaveric donors. Eleven (30%) recipients were five years old or under at the time of transplantation. Of these recipients 44% had complex congenital urologic disease and required urologic surgery prior to or at the time of transplantation. Patients have been followed for a mean of one year, with actual patient and graft survivals of 100% and 97%, respectively. Only one graft has been lost, to severe, early recurrent focal segmental glomerulosclerosis. Four of the 36 patients have had one rejection episode each, all reversed completely. Graft function is stable, with serum creatinine proportionate to age--mean serum creatinine in the children under two years old being 0.4 mg/dl, and in the adolescents 1.3 mg/dl, with two adolescent boys having the highest creatinine levels at 1.8 mg/dl. We conclude that an aggressive approach to immunosuppressive therapy in the early posttransplant period with MALG/OKT3/ATGAM induction and rapid achievement of therapeutic cyclosporine levels prevents rejection and results in excellent patient and graft survival with subsequent stable good graft function.
在1991年5月至1993年4月的两年期间,加利福尼亚太平洋医疗中心对18岁以下儿童进行了36例肾移植手术,采用了积极的四联免疫抑制治疗方案。该方案包括用抗淋巴细胞制剂诱导治疗(21例用马抗淋巴细胞球蛋白,2例用OKT3,12例用抗胸腺细胞球蛋白,1例未用)、初始中等剂量的类固醇治疗、早期静脉注射环孢素治疗和硫唑嘌呤。20例活体亲属供肾受者接受了供者特异性输血预处理。长期环孢素的剂量根据血药浓度调整,以使全血水平(放射免疫分析法)维持在200 - 300 ng/ml。25个移植物来自活体亲属供者,2个来自活体非亲属供者,9个来自尸体供者。11名(30%)受者在移植时年龄为5岁或以下。这些受者中44%患有复杂的先天性泌尿系统疾病,在移植前或移植时需要进行泌尿外科手术。患者平均随访一年,实际患者和移植物存活率分别为100%和97%。仅1个移植物因严重的早期复发性局灶节段性肾小球硬化而丢失。36例患者中有4例各发生1次排斥反应,均完全逆转。移植物功能稳定,血清肌酐与年龄相称——2岁以下儿童的平均血清肌酐为0.4 mg/dl,青少年为1.3 mg/dl,2名青少年男性的肌酐水平最高,为1.8 mg/dl。我们得出结论,在移植后早期采用积极的免疫抑制治疗方法,用马抗淋巴细胞球蛋白/OKT3/抗胸腺细胞球蛋白诱导治疗并迅速达到治疗性环孢素血药浓度,可预防排斥反应,并使患者和移植物存活率良好,随后移植物功能稳定良好。