白细胞清除术
克隆形成试验
低温保存
二甲基亚砜
干细胞
造血干细胞移植
造血
移植
祖细胞
男科
活力测定
造血干细胞
免疫学
生物
化学
川地34
医学
细胞
外科
生物化学
细胞生物学
有机化学
胚胎
作者
Andrzej Smagur,Iwona Mitrus,Sebastian Giebel,Maria Saduś‐Wojciechowska,Jacek Najda,Tomasz Krużel,Tomasz Czerw,Joanna Gliwinska,Mathias Prokop,Magdalena Głowala‐Kosińska,Agata Chwieduk,Jerzy Hołowiecki
出处
期刊:Vox Sanguinis
[Wiley]
日期:2012-10-09
卷期号:104 (3): 240-247
被引量:28
标识
DOI:10.1111/j.1423-0410.2012.01657.x
摘要
Background and Objectives The procedure of autologous hematopoietic stem/progenitor cell transplantation requires cryopreservation. Addition of DMSO is necessary to secure the viability of such cells, but this solvent is potentially toxic to stem cells’ recipient. 10% DMSO solution is used by the majority of transplant centres. The aim of our study was to test if DMSO concentration might be reduced without negative impact on cell recovery and clonogenicity. Materials and Methods Samples were prospectively collected from 20 patients. Small volumes of leukapheresis products were frozen with different cryoprotective mixtures, containing 10%, 7·5%, 5% and 2·5% DMSO, respectively. The quality of cryoprotective mixtures was evaluated based on recovery, viability and clonogenic potential of hematopoietic stem cells after defreezing. Results Reduction in DMSO concentration to 7·5% or lower was associated with decreased recovery of nucleated cells. In contrast, the number of colonies was highest for 7·5% DMSO with significant differences when compared to 10% DMSO solution. Conclusion Reduction in DMSO concentration from 10% to 7·5% may have favourable impact on hematopoietic recovery after autologous transplantation. The findings require confirmation in a clinical setting.
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