Leukocyte Biology Section, National Heart and Lung Institute, Imperial College, London, UK.
J Cell Physiol. 2012 Nov;227(11):3535-8. doi: 10.1002/jcp.24081.
The discovery of the immunosuppressive properties of mesenchymal stromal cells (MSCs) has given new hope to patients suffering from autoimmune diseases as their lack of immunogenicity in addition to their immunosuppressive and regenerative properties makes them an ideal biological agent for the treatment of various disorders ranging from autoimmune diseases to tissue injury. The translational promises of a safer and more effective therapy has however suffered a setback with the recent release of the results from Phase III randomized clinical trial using MSCs for treatment of steroid refractory acute graft-versus-host disease (GvHD), which failed to meet its primary efficacy endpoint. In this review, we will address the current knowledge of the immunosuppressive mechanisms of MSCs from in vitro studies to animal models and then look upon the results obtained from human clinical trials in order to provide failure analysis of negative studies. We will conclude by proposing future directions which could help address this issue and allow rational development of MSCs as an effective and useful cell-based immunotherapeutic.
间充质基质细胞 (MSCs) 的免疫抑制特性的发现,给患有自身免疫性疾病的患者带来了新的希望,因为它们除了具有免疫抑制和再生特性外,缺乏免疫原性,使它们成为治疗各种疾病的理想生物制剂,从自身免疫性疾病到组织损伤。然而,使用间充质基质细胞治疗类固醇难治性急性移植物抗宿主病 (GvHD) 的 III 期随机临床试验的结果最近公布,这一具有更高安全性和有效性的治疗方法的转化前景遭遇了挫折,因为该试验未能达到其主要疗效终点。在这篇综述中,我们将从体外研究到动物模型,讨论间充质基质细胞的免疫抑制机制的现有知识,然后研究从人体临床试验中获得的结果,以提供对阴性研究的失败分析。最后,我们将提出未来的方向,以帮助解决这个问题,并允许间充质基质细胞作为一种有效的、有用的基于细胞的免疫疗法进行合理的开发。