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肾移植后临床操作性耐受:现状与未来挑战。

Clinical operational tolerance after renal transplantation: current status and future challenges.

机构信息

Transplantation Research Immunology Group, Nuffield Department of Surgery, University of Oxford, Oxford, UK.

出版信息

Ann Surg. 2010 Dec;252(6):915-28. doi: 10.1097/SLA.0b013e3181f3efb0.

Abstract

In solid organ transplantation, the achievement of an immunosuppression (IS)-free state [also referred to as clinical operational tolerance (COT)] represents the ultimate goal. Although COT is feasible and safe in selected cases after liver transplantation, it is an exceptional finding after other types of solid organ transplantation. In the field of renal transplantation (RT), approximately 100 cases of COT have been reported to date, mainly in patients who were not compliant with their immunosuppressive regimens or in individuals who had previously received a bone marrow transplant for hematological disorders. On the basis of promising results obtained in animal models, several tolerogenic protocols have been attempted in humans, but most have failed to achieve robust and stable COT after RT. Molecule-based regimens have been largely ineffective, whereas cell-based regimens have provided some encouraging results. In these latter regimens, apart from standard IS, patients usually receive perioperative infusion of donor bone marrow-derived stem cells, which are able to interact with the immune cells of the host and mitigate their response to engraftment. Unfortunately, most renal transplant patients who developed acute rejection-occurring either during the weaning protocol or after complete withdrawal of IS-eventually lost their grafts. Currently, the immune monitoring necessary for predicting the presence and persistence of donor-specific unresponsiveness is not available. Overall, the present review will provide a conceptual framework for COT and conclude that stable and robust COT after RT remains an elusive goal and that the different strategies attempted to date are not yet reproducibly safe or effective.

摘要

在实体器官移植中,实现免疫抑制(IS)自由状态[也称为临床操作性耐受(COT)]是最终目标。虽然在肝移植后,在选定的病例中 COT 是可行且安全的,但在其他类型的实体器官移植后,COT 是一种罕见的发现。在肾移植(RT)领域,迄今为止已报告了大约 100 例 COT,主要发生在不遵守免疫抑制方案的患者或先前因血液疾病接受骨髓移植的患者中。基于在动物模型中获得的有希望的结果,已经在人类中尝试了几种耐受原性方案,但大多数方案在 RT 后都未能实现强大且稳定的 COT。基于分子的方案基本上无效,而基于细胞的方案提供了一些令人鼓舞的结果。在这些后一种方案中,除了标准 IS 外,患者通常还接受供体骨髓源性干细胞的围手术期输注,这些细胞能够与宿主的免疫细胞相互作用,并减轻它们对移植的反应。不幸的是,大多数发生急性排斥反应的肾移植患者——无论是在脱药方案期间还是在完全停止 IS 后——最终失去了他们的移植物。目前,预测供体特异性无反应性的存在和持续存在所需的免疫监测尚不可用。总体而言,本综述将为 COT 提供一个概念框架,并得出结论,RT 后稳定和强大的 COT 仍然是一个难以实现的目标,迄今为止尝试的不同策略尚不能可靠地安全或有效。

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