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1
Donor-specific mesenchymal stem cell infusion in human and nonhuman primate kidney transplantation.供体特异性间充质干细胞输注在人类和非人灵长类动物肾移植中的应用
Am J Transplant. 2025 May 12. doi: 10.1016/j.ajt.2025.05.008.
2
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本文引用的文献

1
OPTN/SRTR 2022 Annual Data Report: Kidney.OPTN/SRTR 2022 年度数据报告:肾脏。
Am J Transplant. 2024 Feb;24(2S1):S19-S118. doi: 10.1016/j.ajt.2024.01.012.
2
The potential of mesenchymal stem cells to induce immune tolerance to allogeneic transplants.间充质干细胞诱导对同种异体移植物免疫耐受的潜力。
Transpl Immunol. 2023 Dec;81:101939. doi: 10.1016/j.trim.2023.101939. Epub 2023 Oct 20.
3
Chimerism-based Tolerance Induction in Clinical Transplantation: Its Foundations and Mechanisms.嵌合抗原耐受诱导在临床移植中的应用:基础与机制。
Transplantation. 2023 Dec 1;107(12):2473-2485. doi: 10.1097/TP.0000000000004589. Epub 2023 Apr 13.
4
Survival Benefit of First Single-Organ Deceased Donor Kidney Transplantation Compared With Long-term Dialysis Across Ages in Transplant-Eligible Patients With Kidney Failure.在适合移植的肾衰竭患者中,与长期透析相比,首次单器官已故供体肾移植在各年龄段的生存获益。
JAMA Netw Open. 2022 Oct 3;5(10):e2234971. doi: 10.1001/jamanetworkopen.2022.34971.
5
Survival for waitlisted kidney failure patients receiving transplantation versus remaining on waiting list: systematic review and meta-analysis.等待肾衰移植患者接受移植与继续等待的生存情况:系统评价和荟萃分析。
BMJ. 2022 Mar 1;376:e068769. doi: 10.1136/bmj-2021-068769.
6
New Creatinine- and Cystatin C-Based Equations to Estimate GFR without Race.新型基于肌酐和胱抑素 C 的估算肾小球滤过率方程,无需考虑种族因素。
N Engl J Med. 2021 Nov 4;385(19):1737-1749. doi: 10.1056/NEJMoa2102953. Epub 2021 Sep 23.
7
Age-related effects on thymic output and homeostatic T cell expansion following depletional induction in renal transplant recipients.肾移植受者耗竭诱导后胸腺输出和稳态 T 细胞扩增的年龄相关影响。
Am J Transplant. 2021 Sep;21(9):3163-3174. doi: 10.1111/ajt.16625. Epub 2021 May 20.
8
Kidney transplantation using alemtuzumab, belatacept, and sirolimus: Five-year follow-up.使用阿仑单抗、贝拉西普和西罗莫司的肾移植:五年随访
Am J Transplant. 2020 Dec;20(12):3609-3619. doi: 10.1111/ajt.16121. Epub 2020 Jun 30.
9
Cost-effectiveness of Deceased-donor Renal Transplant Versus Dialysis to Treat End-stage Renal Disease: A Systematic Review.已故供体肾移植与透析治疗终末期肾病的成本效益:一项系统评价
Transplant Direct. 2020 Jan 13;6(2):e522. doi: 10.1097/TXD.0000000000000974. eCollection 2020 Feb.
10
Kidney transplant tolerance associated with remote autologous mesenchymal stromal cell administration.与远程自体间充质基质细胞给药相关的肾移植耐受
Stem Cells Transl Med. 2020 Apr;9(4):427-432. doi: 10.1002/sctm.19-0185. Epub 2019 Dec 24.

供体特异性间充质干细胞输注在人类和非人灵长类动物肾移植中的应用

Donor-specific mesenchymal stem cell infusion in human and nonhuman primate kidney transplantation.

作者信息

Anwar Imran J, Li Shu, Mulvihill Michael, Schmitz Robin, Shaw Brian, Gao Qimeng, Swan-Nesbit Sherri, Cheatham Lynn A, How Tam, Miller Allison, Williams Kyha, Yin Fang-Fang, Giles William, Kurtzberg Joanne, Chandran Sindhu, Bridges Nancy, Lyakh Lyudmila, Breeden Cynthia, Gandhi Krupa, Sever Michelle, Song Mingqing, He Xu, Kirk Allan D

机构信息

Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.

Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.

出版信息

Am J Transplant. 2025 May 12. doi: 10.1016/j.ajt.2025.05.008.

DOI:10.1016/j.ajt.2025.05.008
PMID:40368061
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12354185/
Abstract

We report the results of 2 independent, concurrently performed studies evaluating the safety and efficacy of donor-derived mesenchymal stromal cell (MSC) infusions in inducing immune-tolerance in nonhuman primate (NHP) and human kidney transplant recipients treated with depletional induction and belatacept/sirolimus maintenance. Fifteen NHPs received rhesus ATG induction and were divided into 3 groups: control (n = 6), pretransplant thymic irradiation (n = 4), and thymic irradiation with monthly donor-MSC infusion (n = 5). Sirolimus was discontinued at day-180, and belatacept at day-365 posttransplant. In humans, 6 patients enrolled in ITN062ST underwent transplantation with alemtuzumab induction; 4 received 12 monthly donor-MSC infusions followed by immunosuppression withdrawal (ISW) if eligible. Donor-MSC infusion was acutely well tolerated in humans and NHPs. Chimerism was not established, and tolerance was not induced in either study. Two of the 5 NHPs that received MSCs rejected while on belatacept monotherapy with detectable donor-specific antibodies. Two patients did not initiate ISW due to de novo donor-specific antibodies and borderline rejection, and 2 patients failed ISW due to reversible rejection. In conclusion, donor MSCs can be given to NHPs or humans repeatedly without acute consequences, but they neither lead to detectable chimerism nor induce tolerance. In a subset of recipients, infused MSCs can be sensitizing.

摘要

我们报告了两项独立且同时进行的研究结果,这些研究评估了供体来源的间充质基质细胞(MSC)输注在诱导非人类灵长类动物(NHP)和接受清除性诱导及贝拉西普/西罗莫司维持治疗的人类肾移植受者免疫耐受方面的安全性和有效性。15只NHP接受了恒河猴抗胸腺细胞球蛋白诱导,并分为3组:对照组(n = 6)、移植前胸腺照射组(n = 4)和每月输注供体MSC的胸腺照射组(n = 5)。西罗莫司在移植后第180天停用,贝拉西普在移植后第365天停用。在人类中,6名参加ITN062ST研究的患者接受了阿仑单抗诱导移植;4名患者接受了12次每月一次的供体MSC输注,若符合条件则随后停用免疫抑制(ISW)。供体MSC输注在人类和NHP中急性耐受性良好。两项研究均未建立嵌合体,也未诱导出耐受性。接受MSC的5只NHP中有2只在接受贝拉西普单药治疗时出现排斥反应,且检测到供体特异性抗体。2名患者因新发供体特异性抗体和临界排斥反应未启动ISW,2名患者因可逆性排斥反应ISW失败。总之,供体MSC可以反复给予NHP或人类而无急性后果,但它们既不会导致可检测到的嵌合体,也不会诱导耐受性。在一部分受者中,输注的MSC可能具有致敏性。