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Towards the Manufacture of Megakaryocytes and Platelets for Clinical Application.迈向用于临床应用的巨核细胞和血小板的制造。
Transfus Med Hemother. 2017 Jun;44(3):165-173. doi: 10.1159/000477261. Epub 2017 May 23.
2
Platelet bioreactor: accelerated evolution of design and manufacture.血小板生物反应器:设计与制造的加速演进
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3
On the Quest for In Vitro Platelet Production by Re-Tailoring the Concepts of Megakaryocyte Differentiation.在重新设计巨核细胞分化概念的基础上,探索体外血小板生成。
Medicina (Kaunas). 2020 Dec 3;56(12):671. doi: 10.3390/medicina56120671.
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[Ex vivo platelet production from induced pluripotent stem cells].[诱导多能干细胞的体外血小板生成]
Rinsho Ketsueki. 2018;59(10):1905-1913. doi: 10.11406/rinketsu.59.1905.
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Megakaryocyte modification of platelets in thrombocytopenia.巨核细胞对血小板减少症中血小板的修饰。
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Transfus Clin Biol. 2017 Sep;24(3):273-276. doi: 10.1016/j.tracli.2017.06.013. Epub 2017 Jun 29.

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Enabling Large-Scale Ex Vivo Production of Megakaryocytes from CD34 Cells Using Gas-Permeable Surfaces.利用透气表面从 CD34 细胞体外大规模生成巨核细胞。
Stem Cells Transl Med. 2019 Jul;8(7):658-670. doi: 10.1002/sctm.18-0160. Epub 2019 Mar 8.

本文引用的文献

1
Platelet bioreactor: accelerated evolution of design and manufacture.血小板生物反应器:设计与制造的加速演进
Platelets. 2017 Jul;28(5):472-477. doi: 10.1080/09537104.2016.1265922. Epub 2017 Jan 23.
2
Progress in bio-manufacture of platelets for transfusion.生物制造用于输血的血小板的进展。
Platelets. 2017 Nov;28(7):649-656. doi: 10.1080/09537104.2016.1257783. Epub 2017 Jan 9.
3
Direct Conversion of Fibroblasts to Megakaryocyte Progenitors.成纤维细胞直接转化为巨核细胞祖细胞。
Cell Rep. 2016 Oct 11;17(3):671-683. doi: 10.1016/j.celrep.2016.09.036.
4
Long-term safety and efficacy of autologous platelet lysate drops for treatment of ocular GvHD.自体血小板裂解液滴剂治疗眼部移植物抗宿主病的长期安全性和有效性。
Bone Marrow Transplant. 2017 Jan;52(1):101-106. doi: 10.1038/bmt.2016.221. Epub 2016 Sep 5.
5
Effective implementation of a patient blood management programme for platelets.有效实施血小板患者血液管理计划。
Transfus Med. 2016 Dec;26(6):422-431. doi: 10.1111/tme.12331. Epub 2016 Aug 10.
6
Advances of blood cell-based drug delivery systems.基于血细胞的药物递送系统的进展
Eur J Pharm Sci. 2017 Jan 1;96:115-128. doi: 10.1016/j.ejps.2016.07.021. Epub 2016 Aug 2.
7
Platelet generation in vivo and in vitro.体内和体外血小板生成
Springerplus. 2016 Jun 21;5(1):787. doi: 10.1186/s40064-016-2384-1. eCollection 2016.
8
Relative impact of a patient blood management program on utilization of all three major blood components.患者血液管理计划对所有三种主要血液成分使用情况的相对影响。
Transfusion. 2016 Sep;56(9):2212-20. doi: 10.1111/trf.13718. Epub 2016 Jul 6.
9
Platelets: handle with care.
Transfus Med. 2016 Oct;26(5):330-338. doi: 10.1111/tme.12327. Epub 2016 Jun 27.
10
Regulation of platelet lifespan in the presence and absence of thrombopoietin signaling.在存在和不存在血小板生成素信号的情况下调节血小板寿命。
J Thromb Haemost. 2016 Sep;14(9):1882-7. doi: 10.1111/jth.13397. Epub 2016 Aug 11.

迈向用于临床应用的巨核细胞和血小板的制造。

Towards the Manufacture of Megakaryocytes and Platelets for Clinical Application.

作者信息

Baigger Anja, Blasczyk Rainer, Figueiredo Constanca

机构信息

Institute for Transfusion Medicine, Hanover Medical School, Hanover, Germany.

出版信息

Transfus Med Hemother. 2017 Jun;44(3):165-173. doi: 10.1159/000477261. Epub 2017 May 23.

DOI:10.1159/000477261
PMID:28626367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5473071/
Abstract

Platelet transfusions are used in standard clinical practice to prevent hemorrhage in patients suffering from thrombocytopenia or platelet dysfunctions. Recently, a constant rise on the demand of platelets for transfusion has been registered. This may be associated with several factors including demographic changes, population aging as well as incidence and prevalence of hematological diseases. In addition, platelet-regenerative properties have been started to be exploited in different areas such as tissue remodeling and anti-cancer therapies. These new applications are also expected to increase the future demand on platelets. Thus, in vitro generated platelets may constitute a highly desirable alternative to meet the rising demand on platelets. Several factors have been considered in the road trip of producing in vitro megakaryocytes and platelets for clinical application. From selection of the cell source, differentiation protocols and culture conditions to the design of optimal bioreactors, several strategies have been proposed to maximize production yields while preserving functionality. This review summarizes new advances in megakaryocyte and platelet differentiation and their production upscaling.

摘要

在标准临床实践中,血小板输注用于预防血小板减少症或血小板功能障碍患者的出血。最近,已记录到对输血用血小板的需求持续上升。这可能与多种因素有关,包括人口结构变化、人口老龄化以及血液疾病的发病率和患病率。此外,血小板再生特性已开始在组织重塑和抗癌治疗等不同领域得到应用。这些新应用预计也会增加未来对血小板的需求。因此,体外生成的血小板可能成为满足不断增长的血小板需求的理想替代方案。在将体外巨核细胞和血小板用于临床应用的过程中,已经考虑了几个因素。从细胞来源的选择、分化方案和培养条件到最佳生物反应器的设计,已经提出了几种策略来在保持功能的同时最大化产量。本综述总结了巨核细胞和血小板分化及其扩大生产方面的新进展。