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Mesenchymal stem cells and their use in therapy: What has been achieved?

机译:间充质干细胞及其在治疗中的用途:已经取得了什么成就?

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The considerable therapeutic potential of human multipotent mesenchymal stromal cells or mesenchymal stem cells (MSCs) has generated increasing interest in a wide variety of biomedical disciplines. Nevertheless, researchers report studies on MSCs using different methods of isolation and expansion, as well as different approaches to characterize them; therefore, it is increasingly difficult to compare and contrast study outcomes. To begin to address this issue, the Mesenchymal and Tissue Stem Cell Committee of the International Society for Cellular Therapy proposed minimal criteria to define human MSCs. First, MSCs must be plastic-adherent when maintained in standard culture conditions (α minimal essential medium plus 20% fetal bovine serum). Second, MSCs must express CD105, CD73 and CD90, and MSCs must lack expression of CD45, CD34, CD14 or CD11b, CD79α or CD19 and HLA-DR surface molecules. Third, MSCs must differentiate into osteoblasts, adipocytes and chondroblasts in vitro. MSCs are isolated from many adult tissues, in particular from bone marrow and adipose tissue. Along with their capacity to differentiate and transdifferentiate into cells of different lineages, these cells have also generated great interest for their ability to display immunomodulatory capacities. Indeed, a major breakthrough was the finding that MSCs are able to induce peripheral tolerance, suggesting that they may be used as therapeutic tools in immune-mediated disorders. Although no significant adverse events have been reported in clinical trials to date, all interventional therapies have some inherent risks. Potential risks for undesirable events, such as tumor development, that might occur while using these stem cells for therapy must be taken into account and contrasted against the potential benefits to patients.
机译:人多能间充质基质细胞或间充质干细胞(MSCs)的巨大治疗潜力已引起人们对各种生物医学学科的日益增长的兴趣。然而,研究人员报告了关于使用不同的分离和扩增方法以及表征它们的方法对MSC进行的研究。因此,比较和对比研究结果变得越来越困难。为了解决这个问题,国际细胞疗法学会的间充质和组织干细胞委员会提出了定义人类MSC的最低标准。首先,在标准培养条件下(α基本培养基和20%胎牛血清)维持时,MSC必须是可塑性的。其次,MSC必须表达CD105,CD73和CD90,而MSC必须缺少CD45,CD34,CD14或CD11b,CD79α或CD19和HLA-DR表面分子的表达。第三,MSC必须在体外分化为成骨细胞,脂肪细胞和成软骨细胞。 MSC是从许多成人组织,特别是从骨髓和脂肪组织中分离出来的。随着它们分化和转分化成不同谱系细胞的能力,这些细胞也因其显示免疫调节能力的能力而引起了极大的兴趣。确实,一项重大突破是发现MSC能够诱导外周耐受,这表明它们可用作免疫介导的疾病的治疗工具。尽管迄今为止在临床试验中尚未报告重大不良事件,但是所有介入疗法都有一些固有的风险。使用这些干细胞进行治疗时可能会发生的不良事件(例如肿瘤发展)的潜在风险必须加以考虑,并与对患者的潜在益处进行对比。

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