Cohen Jeffrey A
Mellen Center, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH, USA.
J Neurol Sci. 2013 Oct 15;333(1-2):43-9. doi: 10.1016/j.jns.2012.12.009. Epub 2013 Jan 4.
Mesenchymal stem cells (MSCs) are pluripotent non-hematopoietic precursor cells that can be isolated from bone marrow and numerous other tissues, culture-expanded to purity, and induced to differentiate in vitro and in vivo into mesodermal derivatives. MSCs exhibit many phenotypic and functional similarities to pericytes. The immunomodulatory, tissue protective, and repair-promoting properties of MSCs demonstrated both in vitro and in animal models make them an attractive potential therapy for MS and other conditions characterized by inflammation and/or tissue injury. Other potential advantages of MSCs as a therapeutic include the relative ease of culture expansion, relative immunoprivilege allowing allogeneic transplantation, and their ability to traffic from blood to areas of tissue allowing intravascular administration. The overall published experience with MSC transplantation in MS is modest, but several small case series and preliminary studies yielded promising results. Several groups, including us, recently initiated formal studies of autologous, culture-expanded, bone marrow-derived MSC transplantation in MS. Although there are several potential safety concerns, to date, the procedure has been well tolerated. Future studies that more definitively assess efficacy also will need to address several technical issues.
间充质干细胞(MSCs)是多能非造血前体细胞,可从骨髓和许多其他组织中分离出来,经培养扩增至纯化,并在体外和体内诱导分化为中胚层衍生物。MSCs与周细胞表现出许多表型和功能上的相似性。MSCs在体外和动物模型中表现出的免疫调节、组织保护和促进修复特性,使其成为治疗多发性硬化症(MS)和其他以炎症和/或组织损伤为特征的疾病的一种有吸引力的潜在疗法。MSCs作为一种治疗方法的其他潜在优势包括相对容易进行培养扩增、相对免疫豁免允许同种异体移植,以及它们能够从血液转移到组织区域从而允许血管内给药。已发表的关于MSCs移植治疗MS的总体经验有限,但一些小病例系列和初步研究取得了有希望的结果。包括我们在内的几个研究小组最近启动了关于自体、培养扩增、骨髓来源的MSCs移植治疗MS的正式研究。尽管存在一些潜在的安全问题,但迄今为止,该程序耐受性良好。未来更明确评估疗效的研究还需要解决几个技术问题。