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基于微载体的工业规模培养中,脐带间充质基质细胞维持免疫调节功能。

Umbilical cord derived mesenchymal stromal cells in microcarrier based industrial scale culture sustain the immune regulatory functions.

作者信息

Kurogi Hikari, Takahashi Atsuko, Isogai Maya, Sakumoto Marimu, Takijiri Takashi, Hori Akiko, Furuno Tetsuo, Koike Tetsuo, Yamada Tetsumasa, Nagamura-Inoue Tokiko, Sakaki-Yumoto Masayo

机构信息

Regenerative Medicine Research & Planning Division, Rohto Pharmaceutical Co., Ltd., Osaka, Japan.

Department of Cell Processing and Transfusion, Research Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

出版信息

Biotechnol J. 2021 Jun;16(6):e2000558. doi: 10.1002/biot.202000558. Epub 2021 Apr 14.

Abstract

Mesenchymal stromal cells (MSCs) have been isolated from numerous sources and are potentially therapeutic against various diseases. Umbilical cord-derived MSCs (UC-MSCs) are considered superior to other tissue-derived MSCs since they have a higher proliferation rate and can be procured using less invasive surgical procedures. However, it has been recently reported that 2D culture systems, using conventional cell culture flasks, limit the mass production of MSCs for cell therapy. Therefore, the development of alternative technologies, including microcarrier-based cell culture in bioreactors, is required for the large-scale production and industrialization of MSC therapy. In this study, we aimed to optimize the culture conditions for UC-MSCs by using a good manufacturing practice (GMP)-compatible serum-free medium, developed in-house, and a small-scale (30 mL) bioreactor, which was later scaled up to 500 mL. UC-MSCs cultured in microcarrier-based bioreactors (MC-UC-MSCs) showed characteristics equivalent to those cultured statically in conventional cell culture flasks (ST-UC-MSCs), fulfilling the minimum International Society for Cellular Therapy criteria for MSCs. Additionally, we report, for the first time, the equivalent therapeutic effect of MC-UC-MSCs and ST-UC-MSCs in immunodeficient mice (graft-versus-host disease model). Lastly, we developed a semi-automated cell dispensing system, without bag-to-bag variation in the filled volume or cell concentration. In summary, our results show that the combination of our GMP-compatible serum-free and microcarrier-based culture systems is suitable for the mass production of MSCs at an industrial scale. Further improvements in this microcarrier-based cell culture system can contribute to lowering the cost of therapy and satisfying several unmet medical needs.

摘要

间充质基质细胞(MSCs)已从多种来源分离出来,对多种疾病具有潜在治疗作用。脐带间充质干细胞(UC-MSCs)被认为优于其他组织来源的间充质干细胞,因为它们具有更高的增殖率,并且可以通过侵入性较小的手术程序获取。然而,最近有报道称,使用传统细胞培养瓶的二维培养系统限制了用于细胞治疗的间充质干细胞的大规模生产。因此,为了实现间充质干细胞治疗的大规模生产和产业化,需要开发替代技术,包括生物反应器中基于微载体的细胞培养。在本研究中,我们旨在通过使用内部开发的符合药品生产质量管理规范(GMP)的无血清培养基和小型(30 mL)生物反应器来优化脐带间充质干细胞的培养条件,该生物反应器随后扩大到500 mL。在基于微载体的生物反应器中培养的脐带间充质干细胞(MC-UC-MSCs)表现出与在传统细胞培养瓶中静态培养的脐带间充质干细胞(ST-UC-MSCs)相当的特性,满足了国际细胞治疗协会对间充质干细胞的最低标准。此外,我们首次报道了MC-UC-MSCs和ST-UC-MSCs在免疫缺陷小鼠(移植物抗宿主病模型)中的等效治疗效果。最后,我们开发了一种半自动细胞分配系统,填充体积或细胞浓度没有袋间差异。总之,我们的结果表明,我们的符合GMP的无血清和基于微载体的培养系统的组合适用于工业规模的间充质干细胞大规模生产。这种基于微载体的细胞培养系统的进一步改进有助于降低治疗成本并满足一些未满足的医疗需求。

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