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脐带血干细胞的未来如何?

What is the future for cord blood stem cells?

机构信息

Molecular Medicine Unit, University of Leeds, St. James's University Hospital, Leeds, U.K. (E-mail,

出版信息

Cytotechnology. 2003 Mar;41(2-3):133-8. doi: 10.1023/A:1024874706356.

DOI:10.1023/A:1024874706356
PMID:19002949
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3466692/
Abstract

Stem and progenitor cells are present in cord blood at a high frequency making these cells a major target population for experimental and clinical studies. Over the past decade there has been considerable developments in cord blood research and transplantation but despite the rapid progress many problems remain. The initial hope that cord blood would be an alternative source of haemopoietic cells for transplantation has been tempered by the fact that there are insufficient cells in most cord blood collections to engraft an adult of average weight. In attempts to increase the cell number, a plethora of techniques for ex-vivo expansion have been developed.These techniques have also proved useful for gene therapy. As cord blood cells possess unique properties this allows them to be utilised as suitable vehicles for gene therapy and long-term engraftment of transduced cells has been achieved. Current work examining the nature of the stem cells present in this haematological source indicates that cord blood contains not only haemopoietic stem cells but also primitive non-haemopoietic cells with high proliferative and developmental potential. As attention focuses on stem cell biology and the controversies surrounding the potential use of embryonic stem cells in treatment of disease, the properties of stem cells from other sources including cord blood are being re-appraised. The purpose of this article is to review some of the current areas of work and highlight biological problems associated with the use of cord blood cells.

摘要

脐带血中存在高频率的干细胞和祖细胞,使这些细胞成为实验和临床研究的主要目标群体。在过去的十年中,脐带血研究和移植取得了相当大的进展,但尽管取得了快速进展,许多问题仍然存在。最初希望脐带血将成为移植造血细胞的替代来源,但事实是,大多数脐带血采集物中的细胞数量不足以植入平均体重的成年人,这一希望受到了抑制。为了增加细胞数量,已经开发了大量的体外扩增技术。这些技术也被证明对基因治疗有用。由于脐带血细胞具有独特的特性,因此可以将它们用作基因治疗的合适载体,并已实现转导细胞的长期植入。目前检查这种血液来源中存在的干细胞性质的工作表明,脐带血不仅含有造血干细胞,还含有具有高增殖和发育潜力的原始非造血细胞。随着人们对干细胞生物学的关注以及围绕胚胎干细胞在疾病治疗中潜在用途的争议,包括脐带血在内的其他来源的干细胞的特性正在重新评估。本文的目的是回顾一些当前的工作领域,并强调与使用脐带血细胞相关的生物学问题。

相似文献

1
What is the future for cord blood stem cells?脐带血干细胞的未来如何?
Cytotechnology. 2003 Mar;41(2-3):133-8. doi: 10.1023/A:1024874706356.
2
Cytokines in haemopoietic progenitor mobilisation for peripheral blood stem cell transplantation.造血祖细胞动员用于外周血干细胞移植中的细胞因子。
Curr Pharm Des. 2002;8(5):379-94. doi: 10.2174/1381612023396122.
3
[Umbilical cord blood as a source of stem cells].[脐带血作为干细胞的来源]
Acta Med Croatica. 2006 Jun;60(3):215-25.
4
CD34 Selection and EX Vivo Expansion of Haemopoietic Progenitor Cells: A Review of Laboratory Methodology.
Hematology. 1997;2(4):261-80. doi: 10.1080/10245332.1997.11746346.
5
Hematopoietic stem cell transplantation using single UM171-expanded cord blood: a single-arm, phase 1-2 safety and feasibility study.使用单一UM171扩增脐血的造血干细胞移植:一项单臂1-2期安全性和可行性研究。
Lancet Haematol. 2020 Feb;7(2):e134-e145. doi: 10.1016/S2352-3026(19)30202-9. Epub 2019 Nov 6.
6
Isolation and therapeutic potential of human haemopoietic stem cells.人造血干细胞的分离与治疗潜力。
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Hematopoietic potential of cryopreserved and ex vivo manipulated umbilical cord blood progenitor cells evaluated in vitro and in vivo.体外和体内评估冷冻保存及体外操作的脐带血祖细胞的造血潜能。
Blood. 1996 Feb 15;87(4):1261-71.
8
Extensive amplification and self-renewal of human primitive hematopoietic stem cells from cord blood.
Blood. 1997 Apr 15;89(8):2644-53.
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Stem cell transplantation (cord blood transplants).干细胞移植(脐血移植)。
Hematology Am Soc Hematol Educ Program. 2004:354-71. doi: 10.1182/asheducation-2004.1.354.
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Notch signaling: from stem cell expansion to improving cord blood transplantation.Notch 信号通路:从干细胞扩增到改善脐血移植。
Expert Rev Hematol. 2010 Aug;3(4):401-4. doi: 10.1586/ehm.10.37.

引用本文的文献

1
Stem cells: From embryology to cellular therapy? An appraisal of the present state of art.干细胞:从胚胎学到细胞治疗?对当前现状的评估。
Cytotechnology. 2004 Mar;44(3):125-41. doi: 10.1007/s10616-004-2067-6.

本文引用的文献

1
Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.慢病毒载体转导NOD/SCID重建造血细胞会导致每个转导细胞出现多个载体整合:存在插入诱变的风险。
Blood. 2003 Feb 15;101(4):1284-9. doi: 10.1182/blood-2002-07-2238. Epub 2002 Oct 17.
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Ex vivo expansion of megakaryocyte progenitors from cryopreserved umbilical cord blood. A potential source of megakaryocytes for transplantation.从冷冻保存的脐带血中体外扩增巨核细胞祖细胞。一种用于移植的潜在巨核细胞来源。
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Transplantation of unrelated donor umbilical cord blood in 102 patients with malignant and nonmalignant diseases: influence of CD34 cell dose and HLA disparity on treatment-related mortality and survival.102例恶性和非恶性疾病患者接受无关供者脐带血移植:CD34细胞剂量和HLA不相合对治疗相关死亡率和生存率的影响
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Transplantation of ex vivo expanded cord blood.体外扩增脐血的移植
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Human erythroid cells produced ex vivo at large scale differentiate into red blood cells in vivo.体外大规模培养的人红细胞在体内可分化为红细胞。
Nat Biotechnol. 2002 May;20(5):467-72. doi: 10.1038/nbt0502-467.
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Ex vivo expansion of stem cells from umbilical cord blood: expression of cell adhesion molecules.脐血干细胞的体外扩增:细胞黏附分子的表达
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7
Ex vivo expansion, maturation, and activation of umbilical cord blood-derived T lymphocytes with IL-2, IL-12, anti-CD3, and IL-7. Potential for adoptive cellular immunotherapy post-umbilical cord blood transplantation.利用白细胞介素-2、白细胞介素-12、抗CD3和白细胞介素-7对脐带血来源的T淋巴细胞进行体外扩增、成熟和激活。脐带血移植后过继性细胞免疫治疗的潜力。
Exp Hematol. 2002 Mar;30(3):245-51. doi: 10.1016/s0301-472x(01)00781-0.
8
Generation of functional and mature dendritic cells from cord blood and bone marrow CD34+ cells by two-step culture combined with calcium ionophore treatment.通过两步培养结合钙离子载体处理从脐血和骨髓CD34+细胞生成功能性成熟树突状细胞。
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In vitro expansion of cord blood does not prevent engraftment of severe combined immunodeficient repopulating cells.
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10
Multilineage differentiation activity by cells isolated from umbilical cord blood: expression of bone, fat, and neural markers.从脐带血中分离的细胞的多谱系分化活性:骨、脂肪和神经标志物的表达
Biol Blood Marrow Transplant. 2001;7(11):581-8. doi: 10.1053/bbmt.2001.v7.pm11760145.