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一种用于临床规模扩增人间充质干/基质细胞的无异种生物反应器系统。

A xenogeneic-free bioreactor system for the clinical-scale expansion of human mesenchymal stem/stromal cells.

作者信息

Dos Santos Francisco, Campbell Andrew, Fernandes-Platzgummer Ana, Andrade Pedro Z, Gimble Jeffrey M, Wen Yuan, Boucher Shayne, Vemuri Mohan C, da Silva Cláudia L, Cabral Joaquim M S

机构信息

Department of Bioengineering and IBB-Institute for Biotechnology and Bioengineering, Instituto Superior Técnico, Universidade de Lisboa, Lisboa, Portugal.

出版信息

Biotechnol Bioeng. 2014 Jun;111(6):1116-27. doi: 10.1002/bit.25187. Epub 2014 Feb 4.

Abstract

The large cell doses (>1 × 10(6)  cells/kg) used in clinical trials with mesenchymal stem/stromal cells (MSC) will require an efficient production process. Moreover, monitoring and control of MSC ex-vivo expansion is critical to provide a safe and reliable cell product. Bioprocess engineering approaches, such as bioreactor technology, offer the adequate tools to develop and optimize a cost-effective culture system for the rapid expansion of human MSC for cellular therapy. Herein, a xenogeneic (xeno)-free microcarrier-based culture system was successfully established for bone marrow (BM) MSC and adipose tissue-derived stem/stromal cell (ASC) cultivation using a 1L-scale controlled stirred-tank bioreactor, allowing the production of (1.1 ± 0.1) × 10(8) and (4.5 ± 0.2) × 10(7) cells for BM MSC and ASC, respectively, after 7 days. Additionally, the effect of different percent air saturation values (%Airsat ) and feeding regime on the proliferation and metabolism of BM MSC was evaluated. No significant differences in cell growth and metabolic patterns were observed under 20% and 9%Airsat . Also, the three different feeding regimes studied-(i) 25% daily medium renewal, (ii) 25% medium renewal every 2 days, and (iii) fed-batch addition of concentrated nutrients and growth factors every 2 days-yielded similar cell numbers, and only slight metabolic differences were observed. Moreover, the immunophenotype (positive for CD73, CD90 and CD105 and negative for CD31, CD80 and HLA-DR) and multilineage differentiative potential of expanded cells were not affected upon bioreactor culture. These results demonstrated the feasibility of expanding human MSC from different sources in a clinically relevant expansion configuration in a controlled microcarrier-based stirred culture system under xeno-free conditions. The further optimization of this bioreactor culture system will represent a crucial step towards an efficient GMP-compliant clinical-scale MSC production system.

摘要

在间充质干/基质细胞(MSC)的临床试验中使用的大细胞剂量(>1×10⁶细胞/千克)需要高效的生产工艺。此外,对MSC体外扩增进行监测和控制对于提供安全可靠的细胞产品至关重要。生物过程工程方法,如生物反应器技术,提供了适当的工具来开发和优化一种具有成本效益的培养系统,用于快速扩增用于细胞治疗的人MSC。在此,使用1升规模的可控搅拌罐生物反应器成功建立了一种无异种(xeno)的基于微载体的培养系统,用于培养骨髓(BM)MSC和脂肪组织来源的干/基质细胞(ASC),在7天后分别产生了(1.1±0.1)×10⁸个细胞和(4.5±0.2)×10⁷个细胞用于BM MSC和ASC。此外,评估了不同空气饱和度百分比(%Airsat)和补料方式对BM MSC增殖和代谢的影响。在20%和9%Airsat下未观察到细胞生长和代谢模式的显著差异。同样,研究的三种不同补料方式——(i)每天更换25%的培养基,(ii)每2天更换25%的培养基,以及(iii)每2天分批补加浓缩营养物和生长因子——产生了相似的细胞数量,并且仅观察到轻微的代谢差异。此外,扩增细胞的免疫表型(CD73、CD90和CD105阳性,CD31、CD80和HLA-DR阴性)和多向分化潜能在生物反应器培养后未受影响。这些结果证明了在无xeno条件下,在基于微载体的可控搅拌培养系统中以临床相关的扩增配置从不同来源扩增人MSC的可行性。进一步优化这种生物反应器培养系统将是迈向符合GMP的高效临床规模MSC生产系统的关键一步。

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