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Scalable Manufacturing of Human Mesenchymal Stromal Cells in the Vertical‐Wheel Bioreactor System: An Experimental and Economic Approach
Authors:Diogo de Sousa Pinto  Cátia Bandeiras  Miguel de Almeida Fuzeta  Carlos A V Rodrigues  Sunghoon Jung  Yas Hashimura  Rong‐Jeng Tseng  William Milligan  Brian Lee  Frederico Castelo Ferreira  Cláudia Lobato da Silva  Joaquim M S Cabral
Institution:1. Department of Bioengineering and iBB, Institute for Bioengineering and Biosciences, Instituto Superior Técnico, Universidade de Lisboa, Avenida Rovisco Pais, Lisboa, 1049‐001 Portugal;2. The Discoveries Center for Regenerative and Precision Medicine, Lisbon Campus, Instituto Superior Técnico, Universidade de Lisboa, Avenida Rovisco Pais, Lisboa, 1049‐001 Portugal;3. Division of Clinical Informatics, Department of Medicine, Beth Israel Deaconess Medical Center, 1330 Beacon Street, Brookline, MA, 02446 USA;4. PBS Biotech Inc, 1183 Calle Suerte, Camarillo, CA, 93012 USA;5. AventaCell Biomedical Corp., Global Center for Medical Innovation (GCMI), 575 14th St NW, Atlanta, GA, 30318 USA
Abstract:Mesenchymal stromal cells (MSC) hold great promise for tissue engineering applications and cell‐based therapies. Large cell doses (>1 × 106 cells kg?1) and Good Manufacturing Practices (GMP)‐compliant processes are however required for clinical purposes. Here, a serum‐ and xenogeneic‐free (S/XF) microcarrier‐based culture system is established for the expansion of human umbilical cord matrix (UCM)‐ and adipose tissue (AT)‐derived MSC using the Vertical‐Wheel system (PBS‐0.1 MAG; PBS Biotech). UCM and AT MSC are expanded to maximum cell densities of 5.3 ± 0.4 × 105 cell mL?1 (n = 3) and 3.6 ± 0.7 × 105 cell mL?1 (n = 3), respectively, after 7 days of culture, while maintaining their identity, according to standard criteria. An economic evaluation of the process transfer from T‐flasks to PBS‐0.1 MAG shows a reduction in the costs associated with the production of a dose for an average 70 kg adult patient (i.e., 70 million cells). Costs decrease from $17.0 K to $11.1 K for UCM MSC and from $21.5 K to $11.1 K for AT MSC, proving that the transition to Vertical‐Wheel reactors provides a cost‐effective alternative for MSC expansion. The present work reports the establishment of a scalable and cost‐effective culture platform for the manufacturing of UCM and AT MSC in a S/XF microcarrier‐based system.
Keywords:economic model  ex vivo expansion  mesenchymal stromal cells  Vertical‐Wheel Bioreactor
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