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Umbilical Cord Tissue as a Source of Young Cells for the Derivation of Induced Pluripotent Stem Cells Using Non-Integrating Episomal Vectors and Feeder-Free Conditions

机译:脐带组织作为幼细细胞来源用于使用非整合性再生载体和无饲养条件衍生诱导多能干细胞

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摘要

The clinical application of induced pluripotent stem cells (iPSC) needs to balance the use of an autologous source that would be a perfect match for the patient against any safety or efficacy issues that might arise with using cells from an older patient or donor. Drs. Takahashi and Yamanaka and the Office of Cellular and Tissue-based Products (PMDA), Japan, have had concerns over the existence of accumulated DNA mutations in the cells of older donors and the possibility of long-term negative effects. To mitigate the risk, they have chosen to partner with the Umbilical Cord (UC) banks in Japan to source allogeneic-matched donor cells. Production of iPSCs from UC blood cells (UCB) has been successful; however, reprogramming blood cells requires cell enrichment with columns or flow cytometry and specialized growth media. These requirements add to the cost of production and increase the manipulation of the cells, which complicates the regulatory approval process. Alternatively, umbilical cord tissue mesenchymal stromal cells (CT-MSCs) have the same advantage as UCB cells of being a source of young donor cells. Crucially, CT-MSCs are easier and less expensive to harvest and grow compared to UCB cells. Here, we demonstrate that CT-MSCs can be easily isolated without expensive enzymatic treatment or columns and reprogramed well using episomal vectors, which allow for the removal of the reprogramming factors after a few passages. Together the data indicates that CT-MSCs are a viable source of donor cells for the production of clinical-grade, patient matched iPSCs.
机译:诱导多能干细胞(IPSC)的临床应用需要平衡使用自体源的使用,这将是患者对患者可能产生的任何安全性或功效问题的完美匹配,这些问题可能与来自较老的患者或供体的细胞产生的任何安全性或功效问题。博士。 Takahashi和Yamanaka以及日本的蜂窝和组织产品办公室(PMDA)已经担心较老捐赠者细胞中积累的DNA突变和长期负面影响的可能性。为了减轻风险,他们选择与日本的脐带(UC)银行合作,以来源同种异体匹配的供体细胞。来自UC血细胞(UCB)的IPSC的生产已经成功;然而,重编程血细胞需要用柱或流式细胞术和专用生长培养基进行细胞富集。这些要求增加了生产成本,增加了细胞的操纵,使监管审批过程复杂化。或者,脐带组织间充质基质细胞(CT-MSCs)具有与作为年轻供体细胞源的UCB细胞相同的优势。至关重要的,与UCB细胞相比,CT-MSCs更容易且较低的成本和成长。在这里,我们证明可以在没有昂贵的酶促治疗或柱子的情况下容易地分离CT-MSC,并且使用再象征载体重新编程,这允许在几次通道后去除重编程因素。这些数据表明CT-MSCs是供体细胞的可行来源,用于生产临床级,患者匹配的IPSC。

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