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Limited Potential or Unfavorable Manipulations? Strategies Toward Efficient Mesenchymal Stem/Stromal Cell Applications

机译:有限的潜在或不利的操纵?高效间充质茎/基质电池应用的策略

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摘要

Despite almost 50 years of research and over 20 years of pre-clinical and clinical studies, the question of curative potential of mesenchymal stem/stromal cells (MSCs) is still widely discussed in the scientific community. Non-reproducible treatment outcomes or even absence of treatment effects in comparison to control groups challenge the potential of these cells for routine application both in tissue engineering and in regenerative medicine. One of the reasons of such outcomes is non-standardized and often disadvantageous ex vivo manipulation of MSCs prior therapy. In most cases, clinically relevant cell numbers for MSC-based therapies can be only obtained by in vitro expansion of isolated cells. In this mini review we will discuss point by point possible pitfalls in the production of human MSCs for cell therapies, without consideration of material-based applications. Starting with cell source, choice of donor and recipient as well as isolation methods, we will then discuss existing expansion protocols (2D/3D cultivation, basal medium, medium supplements, static/dynamic conditions, hypoxic/normoxic conditions) and influence of these strategies on the cell functionality after implantation. The role of potency assays will also be addressed. The final aim of this mini review is the illustration of the heterogeneity of current strategies for gaining MSCs for clinical applications with their strengths and weaknesses. Only a careful consideration and standardization of all pre-treatment processes/methods for the different applications of MSCs will assure robust and reproducible performance of these cell populations in the different experimental and clinical settings.
机译:尽管近50年的研究和20多年的临床前和临床研究,但在科学界仍然广泛讨论了间充质茎/基质细胞(MSCs)的疗中潜力问题。与对照组相比,不可再现的治疗结果或甚至没有治疗效果,攻击这些细胞在组织工程和再生医学中常规应用这些细胞的潜力。这种结果的原因之一是非标准化的,通常是不利的MSCs前治疗方法。在大多数情况下,基于MSC的疗法的临床相关细胞数可以仅通过分离的细胞的体外膨胀而获得。在这个迷你评论中,我们将在不考虑基于材料的应用程序的人体MSCs的人体MSCs生产中,通过点可能的缺陷来讨论点。从细胞来源开始,捐赠者和接受者的选择以及隔离方法,我们将讨论现有的扩展协议(2D / 3D培养,基础培养基,中补充剂,静态/动态条件,缺氧/常规条件)和这些策略的影响植入后细胞功能。还将解决效力测定的作用。这种迷你评论的最终目的是当前策略的异质性,用于使用其优势和劣势获得临床应用的MSCs。只有仔细考虑和标准化MSCs的不同应用程序的所有预处理方法/方法都将在不同的实验和临床环境中确保这些细胞群的稳健和可再现性能。

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