Automated Manufacturing Processes and Platforms for Large-scale Production of Clinical-grade Mesenchymal Stem/ Stromal Cells

被引:1
作者
Strecanska, Magdalena [1 ,2 ]
Sekelova, Tatiana [1 ,2 ]
Smolinska, Veronika [1 ,2 ]
Kuniakova, Marcela [1 ]
Nicodemou, Andreas [1 ,2 ,3 ]
机构
[1] Comenius Univ, Inst Med Biol Genet & Clin Genet, Fac Med, Sasinkova 4, Bratislava 81108, Slovakia
[2] Natl Inst Rheumat Dis, Nabrezie I Krasku 4, Piestany 92101, Slovakia
[3] GAMMA ZA, Kollarova 8, Trencin 91101, Slovakia
关键词
Mesenchymal stem/Stromal Cells (MSCs); Cell Therapy; Good Manufacturing Practice (GMP); Large-scale Production; XENO-FREE CRYOPRESERVATION; HUMAN PLATELET LYSATE; FETAL BOVINE SERUM; BONE-MARROW; ANIMAL SERUM; EXPANSION; ADIPOSE; TECHNOLOGIES; CULTURE; BLOOD;
D O I
10.1007/s12015-024-10812-5
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem/stromal cells (MSCs) hold immense potential for regenerative medicine due to their remarkable regenerative and immunomodulatory properties. However, their therapeutic application requires large-scale production under stringent regulatory standards and Good Manufacturing Practice (GMP) guidelines, presenting significant challenges. This review comprehensively evaluates automated manufacturing processes and platforms for the scalable production of clinical-grade MSCs. Various large-scale culture vessels, including multilayer flasks and bioreactors, are analyzed for their efficacy in MSCs expansion. Furthermore, automated MSCs production platforms, such as Quantum (R) Cell Expansion System, CliniMACS Prodigy (R), NANT001/ XL, CellQualia (TM), Cocoon (R) Platform, and Xuri (TM) Cell Expansion System W25 are reviewed and compared as well. We also underscore the importance of optimizing culture media specifically emphasizing the shift from fetal bovine serum to humanized or serum-free alternatives to meet GMP standards. Moreover, advances in alternative cryopreservation methods and controlled-rate freezing systems, that offer promising improvements in MSCs preservation, are discussed as well. In conclusion, advancing automated manufacturing processes and platforms is essential for realizing the full potential of MSCs-based regenerative medicine and accomplishing the increasing demand for cell-based therapies. Collaborative initiatives involving industry, academia, and regulatory bodies are emphasized to accelerate the translation of MSCs-based therapies into clinical practice.
引用
收藏
页码:372 / 389
页数:18
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