Jenkins Michael J, Farid Suzanne S
Department of Biochemical Engineering, University College London, London, UK.
Biotechnol J. 2015 Jan;10(1):83-95. doi: 10.1002/biot.201400348. Epub 2014 Nov 19.
The ability to develop cost-effective, scalable and robust bioprocesses for human pluripotent stem cells (hPSCs) will be key to their commercial success as cell therapies and tools for use in drug screening and disease modelling studies. This review outlines key process economic drivers for hPSCs and progress made on improving the economic and operational feasibility of hPSC bioprocesses. Factors influencing key cost metrics, namely capital investment and cost of goods, for hPSCs are discussed. Step efficiencies particularly for differentiation, media requirements and technology choice are amongst the key process economic drivers identified for hPSCs. Progress made to address these cost drivers in hPSC bioprocessing strategies is discussed. These include improving expansion and differentiation yields in planar and bioreactor technologies, the development of xeno-free media and microcarrier coatings, identification of optimal bioprocess operating conditions to control cell fate and the development of directed differentiation protocols that reduce reliance on expensive morphogens such as growth factors and small molecules. These approaches offer methods to further optimise hPSC bioprocessing in terms of its commercial feasibility.
开发具有成本效益、可扩展且稳健的人类多能干细胞(hPSC)生物工艺的能力,将是其作为细胞疗法以及用于药物筛选和疾病建模研究工具取得商业成功的关键。本综述概述了hPSC关键的工艺经济驱动因素,以及在提高hPSC生物工艺的经济和操作可行性方面所取得的进展。讨论了影响hPSC关键成本指标(即资本投资和产品成本)的因素。步骤效率,特别是分化效率、培养基要求和技术选择,是确定的hPSC关键工艺经济驱动因素之一。文中讨论了在hPSC生物工艺策略中为应对这些成本驱动因素所取得的进展。这些进展包括提高平面和生物反应器技术中的扩增和分化产量、开发无动物源培养基和微载体涂层、确定控制细胞命运的最佳生物工艺操作条件,以及开发减少对生长因子和小分子等昂贵形态发生素依赖的定向分化方案。这些方法提供了在商业可行性方面进一步优化hPSC生物工艺的途径。