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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Randomized double-blind study of immunoprophylaxis with basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, in combination with mycophenolate mofetil-containing triple therapy in renal transplantation.
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Randomized double-blind study of immunoprophylaxis with basiliximab, a chimeric anti-interleukin-2 receptor monoclonal antibody, in combination with mycophenolate mofetil-containing triple therapy in renal transplantation.

机译:嵌合抗白介素2受体单克隆抗体巴利昔单抗联合含麦考酚酸酯的三联疗法在肾移植中的免疫预防随机双盲研究。

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摘要

BACKGROUND: Acute rejection remains a major problem in renal transplantation. Immunoprophylaxis with basiliximab (Simulect) has achieved significant reductions in acute rejection episodes in renal allograft recipients receiving dual immunosuppression. This study explored the tolerability and cumulative benefit of combining basiliximab with triple-drug therapy-cyclosporine (USP Modified, Neoral), mycophenolate mofetil, and steroids. METHODS: In a randomized, double-blind, placebo-controlled, multicenter study, 123 kidney transplant recipients received either basiliximab at 20 mg before transplantation (day 0) and 20 mg on day 4 (n=59), or placebo (n=64). All received triple-drug immunosuppression and were followed for 6 months. RESULTS: Tolerability of basiliximab was equivalent to placebo, with no increase in serious adverse events, infection, malignancy, or posttransplant lymphoproliferative disorder. At 6 months, there were trends in favor of basiliximab over placebo in the incidences of first biopsy-confirmed acute rejection (15.3% vs. 26.6%, P=NS) and of acute rejection treated with antibody (5.1% vs. 15.6%, P=NS). Kaplan-Meier estimates at 4 weeks and 6 months were significantly in favor of basiliximab treatment for first acute rejection, biopsy-confirmed rejection, rejection episodes treated with antibody therapy, and treatment failure. Renal function improved more rapidly in the basiliximab group, with mean creatinine clearance at week 2 being 54.7 mL/min versus 43.2 mL/min for placebo (P=0.034). At 12 months, patient survival was 100% in both groups; graft survival was 94.9% with basiliximab and 92.2% with placebo. CONCLUSIONS: Basiliximab immunoprophylaxis is safe, well tolerated, and shows a trend toward reduction in number of acute rejection episodes in renal transplant patients receiving cyclosporine, mycophenolate mofetil, and steroids.
机译:背景:急性排斥反应仍然是肾移植的主要问题。使用巴利昔单抗(Simulect)进行免疫预防已显着降低了接受双重免疫抑制的同种异体肾移植受体的急性排斥反应。这项研究探讨了将巴利昔单抗与三药疗法-环孢霉素(USP改良,Neoral),霉酚酸酯和类固醇合用的耐受性和累积益处。方法:在一项随机,双盲,安慰剂对照的多中心研究中,123位肾移植受者在移植前(第0天)和第4天(n = 59)分别以20 mg和20 mg接受巴利昔单抗,或在安慰剂(n = 59)下接受20 mg 64)。所有患者均接受了三药免疫抑制,并随访了6个月。结果:巴利昔单抗的耐受性与安慰剂相当,严重不良事件,感染,恶性肿瘤或移植后的淋巴增生性疾病没有增加。在6个月时,在首次活检确认的急性排斥反应(15.3%比26.6%,P = NS)和经抗体治疗的急性排斥反应(5.1%比15.6%, P = NS)。 Kaplan-Meier在4周和6个月时的估计值显着支持巴利昔单抗治疗的首次急性排斥反应,活检确诊的排斥反应,用抗体疗法治疗的排斥反应发作和治疗失败。巴利昔单抗组的肾功能改善更快,第2周的平均肌酐清除率为54.7 mL / min,而安慰剂为43.2 mL / min(P = 0.034)。在12个月时,两组患者的存活率均为100%。巴利昔单抗的移植物存活率为94.9%,而安慰剂为92.2%。结论:Basiliximab免疫预防是安全的,耐受性良好,并且显示出接受环孢素,霉酚酸酯和类固醇的肾移植患者急性排斥反应发作次数减少的趋势。

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