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肾移植后输注第三方间充质基质细胞:一项 I 期- II 期、开放性标签、临床研究。

Infusion of third-party mesenchymal stromal cells after kidney transplantation: a phase I-II, open-label, clinical study.

机构信息

Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; Groupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Cardiovascular Sciences, University of Liège (ULiège), Liège, Belgium.

Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.

出版信息

Kidney Int. 2019 Mar;95(3):693-707. doi: 10.1016/j.kint.2018.08.046. Epub 2018 Dec 6.

Abstract

Mesenchymal stromal cells (MSCs) exhibit anti-inflammatory and immune-regulatory properties, and preclinical studies suggest a potential benefit in solid organ transplantation. We report on the 1-year follow-up of an open-label phase I-II trial of a single infusion of third-party MSC post-kidney transplantation, in addition to standard immunosuppression. Ten kidney transplant recipients from deceased donors received third-party bone marrow MSCs (∼2 × 10/kg) on day 3 ± 2 post-transplant and were compared to 10 concurrent controls. No adverse effects were noted at MSC injection. One participant with a history of cardiac disease had a non-ST-elevation myocardial infarction approximately 3 hours after MSC infusion. Incidences of opportunistic infections and acute rejection were similar. At day 7 post-transplant, estimated glomerular filtration rate (eGFR) in MSC-treated recipients reached 48.6 ml/min/1.73m, compared to 32.5 ml/min/1.73m in controls and 29.3 ml/min/1.73m in our overall cohort of kidney transplant recipients. No difference in eGFR was found at 1 year. MSC-treated recipients showed increased frequencies of regulatory T cells at day 30, with no significant change in B cell frequencies compared to concurrent controls. Four MSC-treated participants developed antibodies against MSC or shared kidney-MSC HLA, with only 1 with MFI >1500. A single infusion of third-party MSC following kidney transplantation appears to be safe, with one cardiac event of unclear relationship to the intervention. MSC therapy is associated with increased regulatory T cell proportion and with improved early allograft function. Long-term effects, including potential immunization against MSC, remain to be studied.

摘要

间充质基质细胞(MSCs)表现出抗炎和免疫调节特性,临床前研究表明其在实体器官移植中有潜在益处。我们报告了一项开放标签的 I- II 期临床试验的 1 年随访结果,该试验在肾移植后单次输注第三方 MSC,同时使用标准免疫抑制。10 名来自已故供体的肾移植受者在移植后第 3 ± 2 天接受了第三方骨髓 MSC(约 2×10/kg),并与 10 名同期对照进行比较。在 MSC 注射时没有观察到不良反应。一名有心脏病病史的参与者在 MSC 输注后约 3 小时发生非 ST 段抬高型心肌梗死。机会性感染和急性排斥反应的发生率相似。在移植后第 7 天,MSC 治疗组受者的估算肾小球滤过率(eGFR)达到 48.6 ml/min/1.73m,而对照组为 32.5 ml/min/1.73m,我们的整个肾移植受者队列为 29.3 ml/min/1.73m。在 1 年时,eGFR 没有差异。与同期对照组相比,MSC 治疗组在第 30 天的调节性 T 细胞频率增加,但 B 细胞频率没有显著变化。4 名 MSC 治疗组参与者产生了针对 MSC 或共享肾-MSC HLA 的抗体,只有 1 名的 MFI>1500。肾移植后单次输注第三方 MSC 似乎是安全的,有 1 例心脏事件与干预措施的关系不清楚。MSC 治疗与增加调节性 T 细胞比例和改善早期移植物功能有关。长期效果,包括对 MSC 的潜在免疫,仍有待研究。

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