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
Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina, USA.
Am J Transplant. 2025 May 12. doi: 10.1016/j.ajt.2025.05.008.
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.
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。