间充质干细胞治疗在血管化复合异体移植中的免疫调节作用

IF 0.9 Q3 SURGERY
R. Heyes, Andrew Iarocci, Y. Tchoukalova, D. Lott
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引用次数: 9

摘要

本文综述了间充质干细胞(MSCs)在促进血管化复合异体移植(VCA)耐受方面的体外和体内免疫调节作用的最新证据。我们进行了广泛的文献综述,以确定有价值的相关文章。本文回顾了在哺乳动物中接受VCA(或同种异体皮肤移植)并给予MSCs的前瞻性临床前试验。在接受实体器官移植的人群中,血管内输送间充质干细胞的前瞻性临床试验也被确定和回顾。包括16项临床前研究。11项研究比较了MSC单药治疗和无治疗;其中,10例报告移植物存活率提高,8例有统计学意义的延长。8项研究分析了骨髓间充质干细胞治疗作为已证实的免疫抑制方案的辅助疗法的同种异体移植物存活。在这些研究中,每日免疫抑制是短暂的,然后停止。在所有的研究中,接受MSC治疗的动物的无治疗移植物存活在统计学上显著延长。骨髓间充质干细胞已被安全地应用于临床,其在肾移植临床试验中的应用提供了证据,证明它们在临床实践中提高了同种异体移植的耐受性。在临床实践中,MSC诱导疗法有可能克服许多阻碍VCA广泛传播的障碍。在msc诱导的VCA耐受成为临床现实之前,需要进行临床前研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunomodulatory Role of Mesenchymal Stem Cell Therapy in Vascularized Composite Allotransplantation
This review aims to summarize contemporary evidence of the in vitro and in vivo immunomodulatory effects of mesenchymal stem cells (MSCs) in promoting vascularized composite allotransplant (VCA) tolerance. An extensive literature review was performed to identify pertinent articles of merit. Prospective preclinical trials in mammal subjects receiving VCA (or skin allograft) with administration of MSCs were reviewed. Prospective clinical trials with intravascular delivery of MSCs in human populations undergoing solid organ transplant were also identified and reviewed. Sixteen preclinical studies are included. Eleven studies compared MSC monotherapy to no therapy; of these, ten reported improved graft survival, which was statistically significantly prolonged in eight. Eight studies analyzed allograft survival with MSC therapy as an adjunct to proven immunosuppressive regimens. In these studies, daily immunosuppression was transiently delivered and then stopped. In all studies, treatment-free graft survival was statistically significantly prolonged in animals that received MSC therapy. MSCs have been safely administered clinically and their use in renal transplant clinical trials provides evidence that they improve allograft transplant tolerance in clinical practice. There is potential for MSC induction therapy to overcome many of the obstacles to widespread VCA in clinical practice. Preclinical studies are needed before MSC-induced VCA tolerance becomes a clinical reality.
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自引率
4.00%
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审稿时长
16 weeks
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