Beschreibung
Many clinical trials in the field of regenerative medicine using human mesenchymal stromal/stem cells (hMSC) underline the therapeutic potential of these cells. To enable clinical applications with hMSC, an optimal large-scale expansion process is required. Advantageous for these adherent growing cells is the use of suspended microcarriers in a dynamic system (stirred tank reactor). Influencing parameters which are considered in this work are the choice of microcarriers for cell expansion, a defined growth medium, the scale-up procedure, the harvest and the quality analysis. The scaleup of the dynamic expansion of the cells including the harvest were carried out in up to 3 L stirred tank bioreactors. The seed train from small spinner flask to bioreactor scale was carried out via beadtobead transfer without the enzymatic detachment of the cells. A chemically defined medium was used for the expansion in static and dynamic culture conditions. For the detachment of the cells, new proteases from non-mammalian origin were investigated. The cells expanded in static and dynamic conditions showed cell surface marker profiles and differentiability into adipocytes, osteoblasts and chondrocytes as stated by the International Society for Cellular Therapy (ISCT). The expansion in the chemically defined medium did not impair the tested cell quality attributes or indicate cell stress on gene level. A theoretical process analysis of parameters like mixing and oxygen transfer in the stirred tank reactor were used as basis for scale-up design. The microcarrier-based stirred tank reactor offers a good opportunity to generate large amounts of high-quality hMSC under monitored process conditions without the need for uncontrolled pre-cultures in tissue flaks.
