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5%二甲基亚砜(DMSO)和戊聚糖改善了脐带血细胞的冷冻保存效果,优于 10%DMSO。

5% dimethyl sulfoxide (DMSO) and pentastarch improves cryopreservation of cord blood cells over 10% DMSO.

机构信息

Molecular and Clinical Hematology Branch (MCHB), National Institutes of Diabetes and Digestive and Kidney Disorders (NIDDK), National Heart, Lung, and Blood Institute (NHLBI), National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Transfusion. 2010 Oct;50(10):2158-66. doi: 10.1111/j.1537-2995.2010.02684.x. Epub 2010 Oct 4.

Abstract

BACKGROUND

Cell number and viability are important in cord blood (CB) transplantation. While 10% dimethyl sulfoxide (DMSO) is the standard medium, adding a starch to freezing medium is increasingly utilized as a cytoprotectant for the thawing process. Similar to hetastarch, pentastarch has the advantages of faster renal clearance and less effect on the coagulation system.

STUDY DESIGN AND METHODS

We compared a lower DMSO concentration (5%) containing pentastarch with 10% DMSO and performed cell viability assay, colony-forming units (CFUs), and transplantation of CB cells in NOD/SCID IL2Rγ(null) mice.

RESULTS

CB cells in 5% DMSO/pentastarch had similar CD34+, CD3+, and CD19+ cell percentages after thawing as fresh CB cells. CB cells in 5% DMSO/pentastarch had higher viability (83.3±9.23%) than those frozen in 10% DMSO (75.3±11.0%, p<0.05). We monitored cell viability postthaw every 30 minutes. The mean loss in the first 30 minutes was less in the 5% DMSO/pentastarch group. At the end of 3 hours, the viability decreased by a mean of 7.75% for the 5% DMSO/pentastarch and 17.5% for the 10% DMSO groups. CFUs were similar between the two cryopreserved groups. Frozen CB cells engrafted equally well in IL2Rγ(null) mice compared to fresh CB cells up to 24 weeks, and CB cells frozen in 5% DMSO/pentastarch engrafted better than those in 10% DMSO.

CONCLUSION

Our data indicate that the lower DMSO concentration with pentastarch represents an improvement in the CB cryopreservation process and could have wider clinical application as an alternate freezing medium over 10% DMSO.

摘要

背景

细胞数量和活力在脐血(CB)移植中很重要。虽然 10%二甲基亚砜(DMSO)是标准介质,但在冷冻介质中添加淀粉作为解冻过程中的细胞保护剂越来越被广泛使用。与羟乙基淀粉类似,戊聚糖具有更快的肾脏清除率和对凝血系统影响较小的优点。

研究设计和方法

我们比较了含有戊聚糖的低浓度(5%)DMSO 与 10% DMSO,并在 NOD/SCID IL2Rγ(null)小鼠中进行了 CB 细胞的活力测定、集落形成单位(CFU)和移植。

结果

解冻后,5%DMSO/戊聚糖中的 CB 细胞具有与新鲜 CB 细胞相似的 CD34+、CD3+和 CD19+细胞百分比。5%DMSO/戊聚糖中的 CB 细胞活力(83.3±9.23%)高于 10%DMSO 冷冻的 CB 细胞(75.3±11.0%,p<0.05)。我们在解冻后每 30 分钟监测一次细胞活力。在最初的 30 分钟内,5%DMSO/戊聚糖组的平均损失较少。在 3 小时结束时,5%DMSO/戊聚糖组的活力平均下降了 7.75%,10%DMSO 组下降了 17.5%。两个冷冻保存组的 CFU 相似。与新鲜 CB 细胞相比,冷冻 CB 细胞在 IL2Rγ(null)小鼠中同样良好地植入,最长可达 24 周,并且在 5%DMSO/戊聚糖中冷冻的 CB 细胞比在 10%DMSO 中冷冻的 CB 细胞植入更好。

结论

我们的数据表明,含有戊聚糖的低浓度 DMSO 代表了 CB 冷冻保存过程的改进,并且可以作为替代 10%DMSO 的冷冻介质在更广泛的临床应用中使用。

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