Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, QLD 4072, Australia.
Biotechnol Bioeng. 2012 Jul;109(7):1817-26. doi: 10.1002/bit.24425. Epub 2012 Jan 17.
Mesenchymal stem cells (MSC) are emerging as a leading cellular therapy for a number of diseases. However, for such treatments to become available as a routine therapeutic option, efficient and cost-effective means for industrial manufacture of MSC are required. At present, clinical grade MSC are manufactured through a process of manual cell culture in specialized cGMP facilities. This process is open, extremely labor intensive, costly, and impractical for anything more than a small number of patients. While it has been shown that MSC can be cultivated in stirred bioreactor systems using microcarriers, providing a route to process scale-up, the degree of numerical expansion achieved has generally been limited. Furthermore, little attention has been given to the issue of primary cell isolation from complex tissues such as placenta. In this article we describe the initial development of a closed process for bulk isolation of MSC from human placenta, and subsequent cultivation on microcarriers in scalable single-use bioreactor systems. Based on our initial data, we estimate that a single placenta may be sufficient to produce over 7,000 doses of therapeutic MSC using a large-scale process.
间充质干细胞(MSC)正在成为许多疾病的主要细胞治疗方法。然而,为了使这些治疗方法成为常规治疗选择,需要高效且具有成本效益的工业制造 MSC 的方法。目前,临床级 MSC 通过在专门的 cGMP 设施中进行手动细胞培养来制造。该过程是开放式的,非常劳动密集型,成本高昂,对于超过少数患者的数量来说不切实际。虽然已经表明可以使用微载体在搅拌生物反应器系统中培养 MSC,从而提供了扩大生产规模的途径,但实现的数量扩展程度通常受到限制。此外,很少关注从胎盘等复杂组织中分离原代细胞的问题。在本文中,我们描述了从人胎盘批量分离 MSC 的封闭过程的初步开发,以及随后在可扩展的即用型生物反应器系统中在微载体上的培养。根据我们的初步数据,我们估计使用大规模工艺,单个胎盘可能足以生产超过 7000 剂治疗性 MSC。