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肝移植前输注第三方骨髓来源的间充质基质细胞:一项随机对照试验。

Third-party bone marrow-derived mesenchymal stromal cell infusion before liver transplantation: A randomized controlled trial.

机构信息

Aldo & Cele Daccò Clinical Research Center for Rare Diseases, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.

Renal Division, ASST Santi Paolo e Carlo, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy.

出版信息

Am J Transplant. 2021 Aug;21(8):2795-2809. doi: 10.1111/ajt.16468. Epub 2021 Feb 22.

DOI:10.1111/ajt.16468
PMID:33370477
Abstract

Mesenchymal stromal cells (MSC) have emerged as a promising therapy to minimize the immunosuppressive regimen or induce tolerance in solid organ transplantation. In this randomized open-label phase Ib/IIa clinical trial, 20 liver transplant patients were randomly allocated (1:1) to receive a single pretransplant intravenous infusion of third-party bone marrow-derived MSC or standard of care alone. The primary endpoint was the safety profile of MSC administration during the 1-year follow-up. In all, 19 patients completed the study, and none of those who received MSC experienced infusion-related complications. The incidence of serious and non-serious adverse events was similar in the two groups. Circulating Treg/memory Treg and tolerant NK subset of CD56 NK cells increased slightly over baseline, albeit not to a statistically significant extent, in MSC-treated patients but not in the control group. Graft function and survival, as well as histologic parameters and intragraft expression of tolerance-associated transcripts in 1-year protocol biopsies were similar in the two groups. In conclusion, pretransplant MSC infusion in liver transplant recipients was safe and induced mild positive changes in immunoregulatory T and NK cells in the peripheral blood. This study opens the way for a trial on possible tolerogenic efficacy of MSC in liver transplantation. ClinicalTrials.gov identifier: NCT02260375.

摘要

间充质基质细胞(MSC)已成为一种有前途的治疗方法,可以最大限度地减少实体器官移植中的免疫抑制方案或诱导耐受。在这项随机、开放标签的 Ib/IIa 期临床试验中,20 名肝移植患者被随机分配(1:1)接受单次移植前静脉输注第三方骨髓来源的 MSC 或单独标准治疗。主要终点是 MSC 给药在 1 年随访期间的安全性。所有患者均完成了研究,未接受 MSC 治疗的患者均未发生与输注相关的并发症。两组患者严重和非严重不良事件的发生率相似。尽管在 MSC 治疗组患者中,循环 Treg/记忆性 Treg 和耐受 NK 细胞的 CD56 NK 细胞亚群略有增加,但未达到统计学显著程度,而对照组患者则无此变化。两组患者的移植物功能和存活率以及 1 年方案活检中的组织学参数和移植内与耐受相关的转录本表达均相似。总之,肝移植受者移植前输注 MSC 是安全的,并在外周血中诱导免疫调节性 T 和 NK 细胞产生轻微的阳性变化。这项研究为 MSC 在肝移植中可能具有的耐受疗效试验开辟了道路。临床试验标识符:NCT02260375。

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