Centre for Biological Engineering, Department of Chemical Engineering, Loughborough University, Leicestershire, UK.
Regen Med. 2012 Jan;7(1):71-84. doi: 10.2217/rme.11.101.
Human pluripotent stem cells will likely be a significant part of the regenerative medicine-driven healthcare revolution. In order to realize this potential, culture processes must be standardized, scalable and able to produce clinically relevant cell numbers, whilst maintaining critical biological functionality. This review comprises a broad overview of important bioprocess considerations, referencing the development of biopharmaceutical processes in an effort to learn from current best practice in the field. Particular focus is given to the recent efforts to grow human pluripotent stem cells in microcarrier or aggregate suspension culture, which would allow geometric expansion of productive capacity were it to be fully realized. The potential of these approaches is compared with automation of traditional T-flask culture, which may provide a cost-effective platform for low-dose, low-incidence conditions or autologous therapies. This represents the first step in defining the full extent of the challenges facing bioprocess engineers in the exploitation of large-scale human pluripotent stem cell manufacture.
人多能干细胞很可能成为再生医学驱动的医疗保健革命的重要组成部分。为了实现这一潜力,培养过程必须标准化、可扩展,并且能够生产出具有临床相关性的细胞数量,同时保持关键的生物学功能。这篇综述涵盖了重要的生物工艺学考虑因素的广泛概述,参考了生物制药工艺的发展,努力从该领域的当前最佳实践中吸取经验。特别关注的是最近在微载体或聚集物悬浮培养中培养人多能干细胞的努力,这将允许在完全实现的情况下实现生产能力的几何扩展。这些方法的潜力与传统 T 瓶培养的自动化进行了比较,这可能为低剂量、低发生率的情况或自体疗法提供一个具有成本效益的平台。这是定义生物工艺工程师在大规模人多能干细胞制造中的所面临挑战的第一步。