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本文引用的文献

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Extensive ex vivo expansion of functional human erythroid precursors established from umbilical cord blood cells by defined factors.通过定义因子,从脐血细胞中建立了大量体外扩增的功能性人红系前体细胞。
Mol Ther. 2014 Feb;22(2):451-463. doi: 10.1038/mt.2013.201. Epub 2013 Sep 3.
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Scalable expansion of human induced pluripotent stem cells in the defined xeno-free E8 medium under adherent and suspension culture conditions.在无动物源的E8限定培养基中,于贴壁和悬浮培养条件下对人诱导多能干细胞进行可扩展的扩增。
Stem Cell Res. 2013 Nov;11(3):1103-16. doi: 10.1016/j.scr.2013.07.011. Epub 2013 Aug 9.
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Efficient generation of human iPSCs by a synthetic self-replicative RNA.通过合成自我复制 RNA 高效生成人类 iPSCs。
Cell Stem Cell. 2013 Aug 1;13(2):246-54. doi: 10.1016/j.stem.2013.06.001.
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Pluripotent stem cells induced from mouse somatic cells by small-molecule compounds.小分子化合物诱导的小鼠体细胞多能干细胞。
Science. 2013 Aug 9;341(6146):651-4. doi: 10.1126/science.1239278. Epub 2013 Jul 18.
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Stem cell bioengineering strategies to widen the therapeutic applications of haematopoietic stem/progenitor cells from umbilical cord blood.拓宽脐带血造血干/祖细胞治疗应用的干细胞生物工程策略
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Establishment of immortalized human erythroid progenitor cell lines able to produce enucleated red blood cells.建立能够产生无核红细胞的永生化人红系祖细胞系。
PLoS One. 2013;8(3):e59890. doi: 10.1371/journal.pone.0059890. Epub 2013 Mar 22.
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RUNX1a enhances hematopoietic lineage commitment from human embryonic stem cells and inducible pluripotent stem cells.RUNX1a 增强了人类胚胎干细胞和诱导多能干细胞向造血谱系的定向分化。
Blood. 2013 Apr 11;121(15):2882-90. doi: 10.1182/blood-2012-08-451641. Epub 2013 Jan 31.
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Erythropoiesis and globin switching in compound Klf1::Bcl11a mutant mice.复合 Klf1::Bcl11a 突变小鼠的红细胞生成和珠蛋白开关。
Blood. 2013 Mar 28;121(13):2553-62. doi: 10.1182/blood-2012-06-434530. Epub 2013 Jan 29.
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Concise review: production of cultured red blood cells from stem cells.简明综述:干细胞生成培养的红细胞。
Stem Cells Transl Med. 2012 Dec;1(12):927-33. doi: 10.5966/sctm.2012-0097. Epub 2012 Nov 26.
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The switch from fetal to adult hemoglobin.从胎儿血红蛋白向成人血红蛋白的转变。
Cold Spring Harb Perspect Med. 2013 Jan 1;3(1):a011643. doi: 10.1101/cshperspect.a011643.

简明综述:基于干细胞的输血用红细胞生成方法。

Concise review: stem cell-based approaches to red blood cell production for transfusion.

机构信息

Division of Hematology, Department of Medicine, and Stem Cell Program, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Stem Cells Transl Med. 2014 Mar;3(3):346-55. doi: 10.5966/sctm.2013-0054. Epub 2013 Dec 20.

DOI:10.5966/sctm.2013-0054
PMID:24361925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3952923/
Abstract

Blood transfusion is a common procedure in modern medicine, and it is practiced throughout the world; however, many countries report a less than sufficient blood supply. Even in developed countries where the supply is currently adequate, projected demographics predict an insufficient supply as early as 2050. The blood supply is also strained during occasional widespread disasters and crises. Transfusion of blood components such as red blood cells (RBCs), platelets, or neutrophils is increasingly used from the same blood unit for multiple purposes and to reduce alloimmune responses. Even for RBCs and platelets lacking nuclei and many antigenic cell-surface molecules, alloimmunity could occur, especially in patients with chronic transfusion requirements. Once alloimmunization occurs, such patients require RBCs from donors with a different blood group antigen combination, making it a challenge to find donors after every successive episode of alloimmunization. Alternative blood substitutes such as synthetic oxygen carriers have so far proven unsuccessful. In this review, we focus on current research and technologies that permit RBC production ex vivo from hematopoietic stem cells, pluripotent stem cells, and immortalized erythroid precursors.

摘要

输血是现代医学中常见的一种程序,在全世界范围内都有实施;然而,许多国家报告称血液供应不足。即使在目前供应充足的发达国家,预计到 2050 年,血液供应也将不足。在偶尔发生的广泛灾害和危机期间,血液供应也会紧张。从同一血单位中输注血液成分,如红细胞 (RBC)、血小板或中性粒细胞,用于多种目的,并减少同种免疫反应,这种做法越来越常见。即使对于缺乏细胞核和许多抗原细胞表面分子的 RBC 和血小板,也可能发生同种免疫,尤其是在有慢性输血需求的患者中。一旦发生同种免疫,这些患者就需要来自具有不同血型抗原组合的供体的 RBC,这使得在每次发生同种免疫后寻找供体成为一项挑战。替代血液替代品,如合成氧载体,迄今为止尚未成功。在这篇综述中,我们重点介绍了目前允许从造血干细胞、多能干细胞和永生化红系前体细胞体外产生 RBC 的研究和技术。