Koga A, Moreso F J, Seron D, Gil-Vernet S, Cruzado J M, Castelao A M, Grinyó J M
Servei Nefrologia, Hospital Universitari Bellvitge, Barcelona, Spain.
Transplant Proc. 2004 Jun;36(5):1305-7. doi: 10.1016/j.transproceed.2004.05.064.
The addition of induction therapy with antilymphocytic antibodies to cyclosporine (CsA) based immunosuppression, has reduced acute rejection incidence and improved short-term survivals, but has not had well-established effects on long-term renal transplant survival.
We analyzed the long-term allograft outcome of patients included in a prospective randomized clinical study conducted in our center 15 years ago by comparing two strategies: (A) horse antilymphoblast globulin (ALG) given at 10 mg/kg on alternate days to a maximum of 6 doses with low-dose CsA started at 8 mg/kg per day and prednisone at 0.25 mg/kg per day, versus (B) CsA started at 15 mg/kg per day and prednisone at 0.5 mg/kg per day. Diabetic and highly sensitized patients (PRA > 70%) were excluded from the study.
The characteristics of the 50 patients enrolled in each group were not different. Although patient survival was not different (88% in group A vs 77% in group B), recipients treated with ALG showed a lower incidence of acute rejection episodes (20% vs 44%, P = .01) and better death-censored renal allograft survival (57% vs 41%, P = .03). Among rejection-free patients, graft survival was 15% higher in group A (60% vs 45%, P = .12). Multivariate Cox regression analysis showed that an acute rejection episode (relative risk [RR]: 2.44, 95% confidence interval [CI] 1.36-4.39; P = .0029) rather than ALG immunosuppression (RR 0.74, 95% CI 0.41-1.33; P = NS) was an independent predictor of death-censored graft survival.
In summary, we confirmed that concomitant induction therapy with ALG, CsA, and steroids improves long-term renal allograft survival.
在基于环孢素(CsA)的免疫抑制方案中添加抗淋巴细胞抗体诱导治疗,已降低急性排斥反应发生率并改善短期生存率,但对肾移植长期存活的影响尚未明确。
我们通过比较两种策略,分析了15年前在本中心进行的一项前瞻性随机临床研究中患者的长期移植物结局:(A)马抗淋巴细胞球蛋白(ALG),剂量为10mg/kg,隔日给药,最多6剂,联合低剂量CsA,起始剂量为8mg/kg/天,泼尼松剂量为0.25mg/kg/天;(B)CsA起始剂量为15mg/kg/天,泼尼松剂量为0.5mg/kg/天。糖尿病患者和高敏患者(群体反应性抗体[PRA]>70%)被排除在研究之外。
每组纳入的50例患者的特征无差异。虽然患者生存率无差异(A组为88%,B组为77%),但接受ALG治疗的受者急性排斥反应发生率较低(20%对44%,P = 0.01),死亡截断的肾移植存活率更高(57%对41%,P = 0.03)。在无排斥反应的患者中;A组的移植物存活率高15%(60%对45%,P = 0.12)。多因素Cox回归分析显示,急性排斥反应发作(相对危险度[RR]:2.44,95%置信区间[CI]1.36 - 4.39;P = 0.0029)而非ALG免疫抑制(RR 0.74,95%CI 0.41 - 1.33;P = 无显著性差异)是死亡截断移植物存活的独立预测因素。
总之,我们证实ALG、CsA和类固醇联合诱导治疗可提高肾移植长期存活率。