Department of Neurosurgery and Oncology, Brain Tumor Stem Cell Laboratory, The Johns Hopkins School of Medicine, Baltimore, MD 21231, USA.
Curr Stem Cell Res Ther. 2010 Dec;5(4):326-44. doi: 10.2174/157488810793351631.
Cellular therapies represent a new frontier in the treatment of neurological disease. Mesenchymal stem cells (MSCs), which can be harvested from bone marrow, adipose tissue, and umbilical cord blood, among many other sources, possess several qualities which may be used to treat diseases of the central nervous system. MSCs migrate to sites of malignancy, a property which may be used for the treatment of brain cancer. MSCs possess immunosuppressive properties, which may be used for the treatment of neurological disorders with an inflammatory etiology. Finally, MSCs restore injured neural tissue, a property which may be used for the treatment of neural injury. Approximately 23 clinical trials have been completed to date, with many more ongoing, and all have been listed in this review. The long-term safety of MSC-based therapies is not well established, and continues to be one major limitation to clinical translation. More broadly, only a small minority of clinical trials have employed rigorous designs that include prospective randomization, patients from multiple centers, clinically-relevant and reproducible endpoints, and adequate long-term follow-up. These limitations must be addressed before MSCs can enter widespread clinical use. Nevertheless, MSCs represent a promising new approach to treating diseases of the central nervous system that are traditionally associated with morbid outcomes. With additional pre-clinical and clinical studies that focus on their potential benefits as well as dangers, MSCs may one day find translation to clinical use in the setting of neurological disease.
细胞疗法代表了治疗神经疾病的新前沿。间充质干细胞(MSCs)可从骨髓、脂肪组织和脐带血等多种来源中提取,具有多种特性,可用于治疗中枢神经系统疾病。MSCs 迁移到恶性肿瘤部位,这一特性可用于治疗脑癌。MSCs 具有免疫抑制特性,可用于治疗具有炎症病因的神经紊乱。最后,MSCs 可修复受损的神经组织,这一特性可用于治疗神经损伤。迄今为止,已有大约 23 项临床试验完成,还有更多的临床试验正在进行中,所有这些都在本综述中列出。基于 MSC 的治疗的长期安全性尚未得到充分确立,这仍然是临床转化的一个主要限制。更广泛地说,只有少数临床试验采用了严格的设计,包括前瞻性随机化、来自多个中心的患者、与临床相关且可重复的终点以及足够的长期随访。在 MSCs 广泛应用于临床之前,必须解决这些限制。尽管如此,MSCs 代表了一种治疗传统上与不良预后相关的中枢神经系统疾病的有前途的新方法。随着更多针对其潜在益处和危险的临床前和临床研究,MSCs 有朝一日可能会在神经疾病的治疗中转化为临床应用。