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间充质基质细胞治疗肾移植受者的安全性和疗效终点。

Safety and Efficacy Endpoints for Mesenchymal Stromal Cell Therapy in Renal Transplant Recipients.

机构信息

Department of Nephrology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, Netherlands.

Department of Nephrology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, Netherlands ; Department of Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Albinusdreef 2, 2333 ZA Leiden, Netherlands.

出版信息

J Immunol Res. 2015;2015:391797. doi: 10.1155/2015/391797. Epub 2015 Jul 15.

Abstract

Despite excellent short-term graft survival after renal transplantation, the long-term graft outcome remains compromised. It has become evident that a combination of sustained alloreactivity and calcineurin-inhibitor- (CNI-) related nephrotoxicity results in fibrosis and consequently dysfunction of the graft. New immunosuppressive regimens that can minimize or eliminate side effects, while maintaining efficacy, are required to improve long-term graft survival. In this perspective mesenchymal stromal cells (MSCs) are an interesting candidate, since MSCs have immunosuppressive and regenerative properties. The first clinical trials with MSCs in renal transplantation showed safety and feasibility and displayed promising results. Recently, the first phase II studies have been started. One of the most difficult and challenging aspects in those early phase trials is to define accurate endpoints that can measure safety and efficacy of MSC treatment. Since both graft losses and acute rejection rates declined, alternative surrogate markers such as renal function, histological findings, and immunological markers are used to measure efficacy and to provide mechanistic insight. In this review, we will discuss the current status of MSCs in renal transplantation with a focus on the endpoints used in the different experimental and clinical studies.

摘要

尽管肾移植后短期移植物存活率非常高,但长期移植物预后仍不理想。目前已经明确,持续的同种异体反应和钙调磷酸酶抑制剂(CNI)相关的肾毒性会导致纤维化,进而导致移植物功能障碍。需要新的免疫抑制方案,既能最大限度地减少或消除副作用,又能保持疗效,以提高长期移植物存活率。在这方面,间充质基质细胞(MSCs)是一个很有前途的候选物,因为 MSCs 具有免疫抑制和再生特性。首例 MSC 在肾移植中的临床试验显示了其安全性和可行性,并显示出了有希望的结果。最近,已经开始了首批 II 期研究。在这些早期试验中,最困难和最具挑战性的方面之一是确定准确的终点,以衡量 MSC 治疗的安全性和疗效。由于移植物丢失率和急性排斥反应率都有所下降,因此使用替代替代标志物,如肾功能、组织学发现和免疫标志物,来衡量疗效并提供机制见解。在这篇综述中,我们将讨论 MSCs 在肾移植中的现状,并重点介绍不同实验和临床研究中使用的终点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f826/4518147/337a91fd946d/JIR2015-391797.001.jpg

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