首页> 外文会议>International Small Bowel Transplant Symposium >Daclizumab and Alemtuzumab as induction agents in adult intestinal and multivisoeral transplantation: rejections and infections on 40 recipients during the early post-operative period.
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Daclizumab and Alemtuzumab as induction agents in adult intestinal and multivisoeral transplantation: rejections and infections on 40 recipients during the early post-operative period.

机译:Daclizumab和Alemtuzumab作为成人肠道和多含量移植中的诱导剂:在术后期间的40名接受者中排斥和感染。

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Introduction: Allograft rejection in intestinal transplantation is frequent and bacterial, fungal and viral infections related to elevate immunosuppression regimen remain an important post-transplant drawback. Induction therapy has been adopted and allowed improvements in graft and patients survival. Patients and Methods: Between December 2000 and August 2009 we performed 43 intestinal transplants in 42 adult recipients (median age 34.8 +- 9.5 years, M/F: 22/20, isolated/multivisceral graft: 32/11).We compared, during first 30 days post-transplantation, 40 recipients, allocated in two groups, treated with Daclizumab (Zenapax~R - 12 patients: 8 isolated intestinal graft and 4 multivisceral) or Alemtuzumab (Campath-1H~R - 28 patients: 22 isolated intestinal graft and 6 multivisceral). Maintenance immunosuppression was based on Tacrolimus and steroids in the first group and low doses of Tacrolimus in the second one. Results: During first month, 8 Daclizumab recipients (66.6 %) experienced 9 ACRs of mild degree, successfully treated with steroids; 8 patients (66.6%) developed a bacterial infection requiring treatment. We found 14 ACRs in 12 Alemtuzumab recipients (42.8 %), 5 mild degree, 1 moderate and 1 mild-moderate; 16 patients (57.1 %) required treatment for infections. 5-years patient cumulative survival is 66 % for daclizumab recipients and 43 % for alemtuzumab patients; 5-years graft survivals is 66 % for daclizumab recipient and 41 % for alemtuzumab group. In both cases p value is not statistically significative. Discussion and Conclusions: Infection rate is considerably high in both protocols. Alemtuzumab seems to offer a better immunosuppression against ACRs during first month.
机译:介绍:肠道移植中的同种异体移植抑制频繁,与升高免疫抑制方案相关的细菌,真菌和病毒感染仍然是一个重要的移植后缺点。采用诱导疗法并允许改善移植物和患者存活。患者和方法:2000年12月和2009年8月期间,我们在42名成人受者中进行了43位肠移植(中位数34.8 + 9.5岁,M / F:22/20,孤立/多民主壁:32/11)。我们比较,期间移植后30天,40名受者分配两组,用Daclizumab治疗(Zenapax〜R - 12患者:8分离的肠道移植物和4个多念珠)或Alemtuzumab(Campath-1h〜R - 28患者:22例肠道移植物和6个多角度)。维持免疫抑制基于躯干司和第一个组中的类固醇,在第二个组中的低剂量的巨饰血症。结果:在第一个月内,8名Daclizumab受体(66.6%)经历了9亩的轻度程度,用类固醇成功处理; 8名患者(66.6%)开发了需要治疗的细菌感染。我们在12名Alemtuzumab受者(42.8%),5度轻度,1温和的中等; 16名患者(57.1%)需要治疗感染。 5年患者累积存活率为66%,对于酸甲脲受试者为66%,适用于Alemtuzumab患者的43%; Daclizumab受体的5岁移植幸存者为66%,而Alemtuzumab组为41%。在这两种情况下,P值都没有统计学意义。讨论和结论:两种方案中的感染率相当高。 Alemtuzumab似乎在第一个月内对ACRS提供了更好的免疫抑制。

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