Wang Liuqing, Lin Zhenzhen, Shao Bei, Zhuge Qichuan, Jin Kunlin
Department of Neurology, the First Affiliated Hospital, Wenzhou Medical College, China.
Neurol Res. 2013 Jun;35(5):470-8. doi: 10.1179/1743132813Y.0000000210. Epub 2013 Apr 16.
The treatment of ischemic stroke remains a daunting task as few therapeutic strategies have proven effective. Systemic thrombolysis with intravenous tissue plasminogen activator (tPA) remains the only proven treatment to improve clinical outcome of patients with acute ischemic stroke. But because of increased risk of hemorrhage beyond 4·5 hours post-stroke, few stroke patients (1-2%) benefit from tPA. Therefore, new therapies need to be found that protect and repair the damaged brain after stroke. The discovery of stem cells holds great promise for the cure of many diseases, including stroke. The bone marrow-derived stem cells (BMSCs) have particularly gained a great deal of attention, as BMSCs can differentiate into different lineages under specific conditions. In addition, obtaining marrow cells would be easy and using patient's own BMSCs may eliminate the risk of rejection. Therapeutic effects have been reported in animal models of stroke after transplantation of BMSCs. Initial clinical trials using BMSC transplantation have been performed in patients with ischemic stroke. Additional trials are evaluating the impact of BMSCs on safety, feasibility, and efficacy for stroke treatment. However, more information about the appropriate cell type, timing of administration, cell delivery route, and optimal dose for translational applications remains largely unexplored. This article reviews the recent progress and future perspectives in BMSC-based therapy for ischemic stroke, focusing on cell delivery route and time window of cell transplantation for treatment of ischemic stroke in animal models and clinical trials.
由于几乎没有已证实有效的治疗策略,缺血性中风的治疗仍然是一项艰巨的任务。静脉注射组织型纤溶酶原激活剂(tPA)进行全身溶栓仍然是唯一已证实能改善急性缺血性中风患者临床结局的治疗方法。但由于中风后超过4.5小时出血风险增加,很少有中风患者(1%-2%)能从tPA治疗中获益。因此,需要找到新的疗法来保护和修复中风后受损的大脑。干细胞的发现为包括中风在内的许多疾病的治愈带来了巨大希望。骨髓来源的干细胞(BMSCs)尤其受到了广泛关注,因为BMSCs在特定条件下可以分化为不同的细胞谱系。此外,获取骨髓细胞容易,使用患者自身的BMSCs可能消除排斥风险。在BMSCs移植后的中风动物模型中已报道有治疗效果。使用BMSC移植的初步临床试验已在缺血性中风患者中进行。更多试验正在评估BMSCs对中风治疗的安全性、可行性和疗效的影响。然而,关于用于转化应用的合适细胞类型、给药时间、细胞递送途径和最佳剂量的更多信息在很大程度上仍未得到探索。本文综述了基于BMSCs的缺血性中风治疗的最新进展和未来前景,重点关注动物模型和临床试验中用于治疗缺血性中风的细胞递送途径和细胞移植时间窗。