Kalladka Dheeraj, Muir Keith W
Institute of Neuroscience and Psychology, University of Glasgow, Southern General Hospital, Glasgow, United Kingdom.
Stem Cells Cloning. 2014 Feb 21;7:31-44. doi: 10.2147/SCCAA.S38003. eCollection 2014.
Stroke affects one in every six people worldwide, and is the leading cause of adult disability. Some spontaneous recovery is usual but of limited extent, and the mechanisms of late recovery are not completely understood. Endogenous neurogenesis in humans is thought to contribute to repair, but its extent is unknown. Exogenous cell therapy is promising as a means of augmenting brain repair, with evidence in animal stroke models of cell migration, survival, and differentiation, enhanced endogenous angiogenesis and neurogenesis, immunomodulation, and the secretion of trophic factors by stem cells from a variety of sources, but the potential mechanisms of action are incompletely understood. In the animal models of stroke, both mesenchymal stem cells (MSCs) and neural stem cells (NSCs) improve functional recovery, and MSCs reduce the infarct volume when administered acutely, but the heterogeneity in the choice of assessment scales, publication bias, and the possible confounding effects of immunosuppressants make the comparison of effects across cell types difficult. The use of adult-derived cells avoids the ethical issues around embryonic cells but may have more restricted differentiation potential. The use of autologous cells avoids rejection risk, but the sources are restricted, and culture expansion may be necessary, delaying treatment. Allogeneic cells offer controlled cell numbers and immediate availability, which may have advantages for acute treatment. Early clinical trials of both NSCs and MSCs are ongoing, and clinical safety data are emerging from limited numbers of selected patients. Ongoing research to identify prognostic imaging markers may help to improve patient selection, and the novel imaging techniques may identify biomarkers of recovery and the mechanism of action for cell therapies.
中风影响着全球六分之一的人口,是成人残疾的主要原因。通常会有一定程度的自发恢复,但程度有限,且后期恢复的机制尚未完全明确。人们认为内源性神经发生有助于修复,但其程度尚不清楚。外源性细胞疗法作为增强脑修复的一种手段很有前景,在动物中风模型中有证据表明,来自多种来源的干细胞可发生细胞迁移、存活和分化,增强内源性血管生成和神经发生,进行免疫调节并分泌营养因子,但其潜在作用机制尚未完全明确。在中风动物模型中,间充质干细胞(MSC)和神经干细胞(NSC)均可改善功能恢复,急性给药时MSC可减小梗死体积,但评估量表选择的异质性、发表偏倚以及免疫抑制剂可能产生的混杂效应使得不同细胞类型之间的效果比较变得困难。使用成体来源的细胞可避免围绕胚胎细胞的伦理问题,但可能具有更有限的分化潜能。使用自体细胞可避免排斥风险,但来源有限,可能需要进行培养扩增,从而延迟治疗。异体细胞可提供可控的细胞数量并可立即使用,这可能对急性治疗具有优势。NSC和MSC的早期临床试验正在进行中,有限数量的特定患者的临床安全性数据也正在出现。正在进行的确定预后成像标志物的研究可能有助于改善患者选择,而新的成像技术可能会识别恢复的生物标志物以及细胞疗法的作用机制。