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首页> 外文期刊>Trials >Allogeneic mesenchymal stem cell as induction therapy to prevent both delayed graft function and acute rejection in deceased donor renal transplantation: study protocol for a randomized controlled trial
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Allogeneic mesenchymal stem cell as induction therapy to prevent both delayed graft function and acute rejection in deceased donor renal transplantation: study protocol for a randomized controlled trial

机译:同种异体间充质干细胞作为诱导治疗可防止已故供体肾移植中移植物功能延迟和急性排斥反应:一项随机对照试验的研究方案

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Using kidneys from deceased donors is an available strategy to meet the growing need of grafts. However, higher incidences of delayed graft function (DGF) and acute rejection exert adverse effects on graft outcomes. Since ischemia-reperfusion injury (IRI) and ongoing process of immune response to grafts are the major causes of DGF and acute rejection, the optimal induction intervention should possess capacities of both repairing renal structure injury and suppressing immune response simultaneously. Mesenchymal stem cells (MSCs) with potent anti-inflammatory, regenerative and immune-modulatory properties are considered as a candidate to prevent both DGF and acute rejection in renal transplantation. Previous studies just focused on the safety of autologous MSCs on living-related donor renal transplants, and lack of concomitant controls and the sufficient sample size and source of MSCs. Here, we propose a prospective multicenter controlled study to assess the clinical value of allogeneic MSCs in preventing both DGF and acute rejection simultaneously as induction therapy in deceased-donor renal transplantation. Renal allograft recipients (n?=?100) will be recruited and divided into trial and control groups, and 50 patients in the trial group will be administered with a dose of 2?×?106 per kilogram human umbilical-cord-derived MSCs (UC-MSCs) via peripheral vein injection preoperatively, and a dose of 5?×?106 cells via renal arterial injection during surgery, with standard induction therapy. Incidences of postoperative DGF and biopsy-proved acute rejection (BPAR) will be recorded and analyzed. Additionally, other clinical parameters such as baseline demographics, graft and recipient survival and other severe postoperative complications, including complicated urinary tract infection, severe pneumonia, and severe bleeding, will be also assessed. This study will clarify the clinical value of UC-MSCs in preventing DGF and acute rejection simultaneously in deceased-donor renal transplantation, and provide evidence as to whether allogeneic MSCs can be used as clinically feasible and safe induction therapy. ClinicalTrials.gov, NCT02490020 . Registered on 29 June 2015.
机译:使用死者捐赠者的肾脏是一种可以满足日益增长的移植需求的可行策略。但是,较高的延迟移植功能(DGF)和急性排斥反应的发生率会对移植结果产生不利影响。由于缺血再灌注损伤(IRI)和持续的移植物免疫反应过程是DGF和急性排斥反应的主要原因,因此最佳诱导干预措施应具有修复肾结构损伤和同时抑制免疫反应的能力。具有强大的抗炎,再生和免疫调节特性的间充质干细胞(MSC)被认为是预防DGF和肾移植急性排斥反应的候选药物。先前的研究仅关注自体MSC在与生命相关的供体肾移植中的安全性,缺乏伴随的对照以及足够的MSC样本量和来源。在这里,我们提出了一项前瞻性多中心对照研究,以评估同种异体间充质干细胞作为死者肾移植的诱导疗法,同时预防DGF和急性排斥反应的临床价值。招募肾脏同种异体移植受者(n = 100)分为试验组和对照组,试验组中的50名患者将按每千克人脐带来源的MSCs剂量2?×?106(术前通过外周静脉注射(UC-MSCs),并在手术过程中通过标准的诱导疗法通过肾动脉注射注射5××106个细胞。术后DGF和活检证实的急性排斥反应(BPAR)的发生率将被记录和分析。此外,还将评估其他临床参数,例如基线人口统计学,移植物和受体的存活以及其他严重的术后并发症,包括复杂的尿路感染,严重的肺炎和严重的出血。这项研究将阐明UC-MSCs在预防供体肾移植中同时预防DGF和急性排斥反应方面的临床价值,并提供同种异体MSCs是否可以用作临床上可行和安全的诱导疗法的证据。 ClinicalTrials.gov,NCT02490020。 2015年6月29日注册。

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