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脐带血单个核细胞在间充质干细胞上的体外扩增

Ex vivo expansion of cord blood mononuclear cells on mesenchymal stem cells.

作者信息

McNiece I, Harrington J, Turney J, Kellner J, Shpall E J

机构信息

Johns Hopkins University School of Medicine Sidney Kimmel Comprehensive Cancer Center Baltimore, MD 21231, USA.

出版信息

Cytotherapy. 2004;6(4):311-7. doi: 10.1080/14653240410004871.

Abstract

BACKGROUND

Cord blood (CB) cells are being used increasingly as a source of hematopoietic cells to support high dose chemotherapy. However, CB units contain low numbers of cells, including CD34+ cells, and thus their use is associated with significant delays in engraftment of neutrophils and platelets. Exvivo expansion of CB has been proposed to increase the numbers of cells available. We and others have reported the requirement of CD34 selection for optimal expansion of CB products'; however, the selection of frozen CB products in clinical trials results in significant loss of CD34+ cells, with a median recovery of 50, but less than 40% recovery in more than one-third of products. In the present studies we evaluated the potential of mesenchymal stem cells (MSC) to support ex vivo expansion of unselected CB products.

METHODS

Mononuclear cells (MNC) from CB products were isolated and cultured on preformed MSC layers in T150 flasks containing 50 mL Stemline II media plus hematopoietic growth factors. Various culture conditions were compared for optimal expansion of the CB MNC.

RESULTS

Ex vivo expansion of CB MNC on MSC resulted in 10- to 20-fold expansion of total nucleated cells, seven- to 18-fold expansion of committed progenitor cells, two- to five-fold expansion of primitive progenitor cells and 16- to 37-fold expansion of CD34+ cells.

DISCUSSION

These studies demonstrated significant expansion of CB products without CD34 cell selection using culture conditions that are clinically applicable. Our current focus is to initiate clinical trials to evaluate the in vivo potential of CB cells expanded with these conditions.

摘要

背景

脐带血(CB)细胞越来越多地被用作造血细胞来源以支持大剂量化疗。然而,脐带血单位所含细胞数量较少,包括CD34+细胞,因此其使用与中性粒细胞和血小板植入的显著延迟有关。有人提出对脐带血进行体外扩增以增加可用细胞数量。我们和其他人已经报道了CD34选择对于脐带血产品最佳扩增的必要性;然而,在临床试验中选择冷冻脐带血产品会导致CD34+细胞大量损失,中位数回收率为50%,但超过三分之一的产品回收率低于40%。在本研究中,我们评估了间充质干细胞(MSC)支持未选择的脐带血产品体外扩增的潜力。

方法

从脐带血产品中分离出单核细胞(MNC),并在含有50 mL Stemline II培养基加造血生长因子的T150培养瓶中的预先形成的MSC层上进行培养。比较了各种培养条件以实现脐带血MNC的最佳扩增。

结果

脐带血MNC在MSC上的体外扩增导致有核细胞总数扩增10至20倍,定向祖细胞扩增7至18倍,原始祖细胞扩增2至5倍,CD34+细胞扩增16至37倍。

讨论

这些研究表明,使用临床适用的培养条件,在不进行CD34细胞选择的情况下,脐带血产品可实现显著扩增。我们目前的重点是启动临床试验,以评估在这些条件下扩增的脐带血细胞的体内潜力。

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