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Prospective flow cytometric evaluation of nucleated red blood cells in cord blood units and relationship with nucleated and CD34(+) cell quantification.脐带血单位中有核红细胞的前瞻性流式细胞术评估及其与有核细胞和CD34(+)细胞定量的关系。
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Detecting primitive hematopoietic stem cells in total nucleated and mononuclear cell fractions from umbilical cord blood segments and units.从脐带血段和单位的总核细胞和单核细胞部分中检测原始造血干细胞。
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本文引用的文献

1
Optimum storage conditions for cord blood-derived hematopoietic progenitor cells prior to isolation.
Bone Marrow Transplant. 2007 Nov;40(9):837-42. doi: 10.1038/sj.bmt.1705831. Epub 2007 Sep 3.
2
Time and temperature before processing influence the recovery of umbilical cord blood hematopoietic progenitors.处理前的时间和温度会影响脐带血造血祖细胞的恢复。
Transfusion. 2007 Aug;47(8):1550-2. doi: 10.1111/j.1537-2995.2007.01351.x.
3
Prediction of engraftment after autologous peripheral blood progenitor cell transplantation: CD34, colony-forming unit-granulocyte-macrophage, or both?自体外周血祖细胞移植后植入的预测:CD34、粒-巨噬细胞集落形成单位,还是两者联合?
Transfusion. 2007 May;47(5):817-23. doi: 10.1111/j.1537-2995.2007.01195.x.
4
Infectious complications following unrelated cord blood transplantation.
Vox Sang. 2007 May;92(4):289-96. doi: 10.1111/j.1423-0410.2007.00900.x.
5
CD34+ cell content for selecting umbilical cord blood units for cryopreservation.用于选择脐带血单位进行冷冻保存的CD34+细胞含量。
Transfusion. 2007 Mar;47(3):552-3. doi: 10.1111/j.1537-2995.2006.01149.x.
6
Efficient enucleation of erythroblasts differentiated in vitro from hematopoietic stem and progenitor cells.从造血干细胞和祖细胞体外分化的成红细胞中高效去核。
Nat Biotechnol. 2006 Oct;24(10):1255-6. doi: 10.1038/nbt1245. Epub 2006 Sep 17.
7
Analysis and cryopreservation of hematopoietic stem and progenitor cells from umbilical cord blood.脐带血造血干细胞和祖细胞的分析与冷冻保存
Cytotherapy. 2006;8(3):265-76. doi: 10.1080/14653240600735685.
8
Optimizing umbilical cord blood collection: impact of obstetric factors versus quality of cord blood units.优化脐带血采集:产科因素与脐带血单位质量的影响
Transplant Proc. 2006 May;38(4):1174-6. doi: 10.1016/j.transproceed.2006.03.052.
9
Umbilical cord nucleated red blood cell counts: normal values and the effect of labor.脐带中有核红细胞计数:正常值及分娩的影响。
J Perinatol. 2006 Feb;26(2):89-92. doi: 10.1038/sj.jp.7211437.
10
Characterization of banked umbilical cord blood hematopoietic progenitor cells and lymphocyte subsets and correlation with ethnicity, birth weight, sex, and type of delivery: a Cord Blood Transplantation (COBLT) Study report.库存脐带血造血祖细胞和淋巴细胞亚群的特征及其与种族、出生体重、性别和分娩方式的相关性:一项脐带血移植(COBLT)研究报告
Transfusion. 2005 Jun;45(6):856-66. doi: 10.1111/j.1537-2995.2005.04429.x.

脐血捐献质量参数评估

Evaluation of Quality Parameters for Cord Blood Donations.

作者信息

Salge-Bartels Ursula, Huber Helga Marie, Kleiner Kornelia, Volkers Peter, Seitz Rainer, Heiden Margarethe

机构信息

Division of Hematology/Transfusion Medicine, Paul Ehrlich Institute, Langen, Germany.

出版信息

Transfus Med Hemother. 2009;36(5):317-324. doi: 10.1159/000232384. Epub 2009 Aug 21.

DOI:10.1159/000232384
PMID:21076550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2969129/
Abstract

SUMMARY

BACKGROUND: Umbilical cord blood (CB) is widely used for hematopoietic stem cell transplantation and holds promise for the development of innovative medicinal products. In order to find out whether the conditions for collection and storage before processing might have an impact on the quality of CB preparations, viability and the clonogenic potential were assessed. METHODS: CB was collected under field conditions. Flow cytometry was used to determine leukocytes, CD34/CD45+ cells, viability, and nucleated red blood cells (NRBC). Clonogenic activity was determined using isolated mononuclear cells (MNC). RESULTS: Neither plasma citrate concentrations nor storage temperature (within 24 h) affected cell viability or colony formation. After storage for 49-80 h, leukocyte viability declined by about 16% compared to CB stored up to 24 h. In contrast, the clonogenic activity and CD34/CD45+ cell content were not affected. A higher gestational age was associated with a lower yield of clonogenic activity compared to midterm deliveries. NRBC varied widely (median 7.3%; range 0.63-17.3%) without relation to gestational age or colony formation. There was a close correlation between the percentage of viable CD34/CD45+ cells and colony formation (r = 0.77 for CFU-GM; r = 0.75 for CFU-C). CONCLUSIONS: The content of viable CD34/CD45+ cells represents the clonogenic activity of CB preparations. Therefore, determination of viable CD34/CD45+ cells should be generally performed as a routine quality control assay.

摘要

摘要

背景:脐带血(CB)被广泛用于造血干细胞移植,并有望开发创新型医药产品。为了弄清楚处理前的采集和储存条件是否会对CB制剂的质量产生影响,对其活力和克隆形成潜力进行了评估。方法:在现场条件下采集CB。采用流式细胞术测定白细胞、CD34/CD45+细胞、活力和有核红细胞(NRBC)。使用分离的单核细胞(MNC)测定克隆形成活性。结果:血浆柠檬酸盐浓度和储存温度(24小时内)均未影响细胞活力或集落形成。储存49 - 80小时后,与储存长达24小时的CB相比,白细胞活力下降了约16%。相比之下,克隆形成活性和CD34/CD45+细胞含量未受影响。与中期分娩相比,较高的胎龄与较低的克隆形成活性产量相关。NRBC差异很大(中位数7.3%;范围0.63 - 17.3%),与胎龄或集落形成无关。存活的CD34/CD45+细胞百分比与集落形成之间存在密切相关性(CFU - GM的r = 0.77;CFU - C的r = 0.75)。结论:存活的CD34/CD45+细胞含量代表了CB制剂的克隆形成活性。因此,一般应将测定存活的CD34/CD45+细胞作为常规质量控制检测方法。