An Integrated Approach toward the Biomanufacturing of Engineered Cell Therapy Products in a Stirred-Suspension Bioreactor

Recent advances in stem cell biology have accelerated the pre-clinical development of cell-based therapies for degenerative and chronic diseases. The success of this growing area hinges upon the concomitant development of scalable manufacturing platforms that can produce clinically relevant quantities of cells for thousands of patients. Current biomanufacturing practices for cell therapy products are built on a model previously optimized for biologics, wherein stable cell lines are established first, followed by large-scale production in the bioreactor. This “two-step” approach can be costly, labor-intensive, and time-consuming, particularly for cell therapy products that must be individually sourced from patients or compatible donors. In this report, we describe a “one-step” integrated approach toward the biomanufacturing of engineered cell therapy products by direct transfection of primary human fibroblast in a continuous stirred-suspension bioreactor. We optimized the transfection efficiency by testing rate-limiting factors, including cell seeding density, agitation rate, oxygen saturation, microcarrier type, and serum concentration. By combining the genetic modification step with the large-scale expansion step, this not only removes the need for manual handing of cells in planar culture dishes, but also enables the biomanufacturing process to be streamlined and automated in one fully enclosed bioreactor.

[1]  Mauro Giacca,et al.  Virus-mediated gene delivery for human gene therapy. , 2012, Journal of controlled release : official journal of the Controlled Release Society.

[2]  M. S. Kallos,et al.  Shear stress influences the pluripotency of murine embryonic stem cells in stirred suspension bioreactors , 2014, Journal of tissue engineering and regenerative medicine.

[3]  Shulan Tian,et al.  Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells , 2007, Science.

[4]  R. Orentas,et al.  Towards a commercial process for the manufacture of genetically modified T cells for therapy , 2015, Cancer Gene Therapy.

[5]  D. Rancourt,et al.  A novel method for generating xeno-free human feeder cells for human embryonic stem cell culture. , 2008, Stem cells and development.

[6]  H. Uludaǧ,et al.  Improved transfection efficiency of an aliphatic lipid substituted 2 kDa polyethylenimine is attributed to enhanced nuclear association and uptake in rat bone marrow stromal cell , 2011, The journal of gene medicine.

[7]  Michel Sadelain,et al.  Manufacturing Validation of Biologically Functional T Cells Targeted to CD19 Antigen for Autologous Adoptive Cell Therapy , 2009, Journal of immunotherapy.

[8]  Nesrine Z. Mostafa,et al.  Modification of human BMSC with nanoparticles of polymeric biomaterials and plasmid DNA for BMP-2 secretion. , 2013, The Journal of surgical research.

[9]  M. Dullaers,et al.  Side-by-side comparison of lentivirally transduced and mRNA-electroporated dendritic cells: implications for cancer immunotherapy protocols. , 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

[10]  Mehdi Shafa,et al.  Derivation of iPSCs in stirred suspension bioreactors , 2012, Nature Methods.

[11]  H. Uludaǧ,et al.  Nucleic-acid based gene therapeutics: delivery challenges and modular design of nonviral gene carriers and expression cassettes to overcome intracellular barriers for sustained targeted expression , 2012, Journal of drug targeting.

[12]  Gang Wang,et al.  Conversion of mouse fibroblasts into cardiomyocytes using a direct reprogramming strategy , 2011, Nature Cell Biology.

[13]  G. Blüml Microcarrier Cell Culture Technology , 2007 .

[14]  H. Deng,et al.  Pluripotent Stem Cells Induced from Mouse Somatic Cells by Small-Molecule Compounds , 2013, Science.

[15]  H. Yoshikawa,et al.  Direct Induction of Chondrogenic Cells from Human Dermal Fibroblast Culture by Defined Factors , 2013, PloS one.

[16]  S. Kimber,et al.  Directed differentiation of human embryonic stem cells toward chondrocytes , 2010, Nature Biotechnology.

[17]  M. S. Kallos,et al.  Efficient suspension bioreactor expansion of murine embryonic stem cells on microcarriers in serum‐free medium , 2011, Biotechnology progress.

[18]  T. Ichisaka,et al.  Induction of Pluripotent Stem Cells From Adult Human Fibroblasts by Defined Factors , 2008 .

[19]  G. Gao,et al.  State-of-the-art human gene therapy: part I. Gene delivery technologies. , 2014, Discovery medicine.

[20]  J. Crook,et al.  Efficient expansion of clinical-grade human fibroblasts on microcarriers: cells suitable for ex vivo expansion of clinical-grade hESCs. , 2008, Journal of biotechnology.

[21]  Todd C McDevitt,et al.  The multiparametric effects of hydrodynamic environments on stem cell culture. , 2011, Tissue engineering. Part B, Reviews.

[22]  S. Reuveny,et al.  Application of human mesenchymal and pluripotent stem cell microcarrier cultures in cellular therapy: achievements and future direction. , 2013, Biotechnology advances.

[23]  S. Yamanaka,et al.  An Efficient Nonviral Method to Generate Integration‐Free Human‐Induced Pluripotent Stem Cells from Cord Blood and Peripheral Blood Cells , 2013, Stem cells.

[24]  Melissa A. Kinney,et al.  Hydrodynamic modulation of pluripotent stem cells , 2012, Stem Cell Research & Therapy.

[25]  J. Polak,et al.  Stem Cells Bioprocessing: An Important Milestone to Move Regenerative Medicine Research Into the Clinical Arena , 2008, Pediatric Research.

[26]  K. L. Douglas Toward Development of Artificial Viruses for Gene Therapy: A Comparative Evaluation of Viral and Non‐viral Transfection , 2008, Biotechnology progress.

[27]  K. Shakesheff,et al.  Directed differentiation of human embryonic stem cells to interrogate the cardiac gene regulatory network. , 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

[28]  林欣榮,et al.  Functional Cells Cultured on Microcarriers for Use in Regenerative Medicine Research. , 2011 .

[29]  M. S. Kallos,et al.  Non-viral engineering of skin precursor-derived Schwann cells for enhanced NT-3 production in adherent and microcarrier culture. , 2012, Current medicinal chemistry.

[30]  Krishnendu Roy,et al.  Biomanufacturing of Therapeutic Cells: State of the Art, Current Challenges, and Future Perspectives. , 2016, Annual review of chemical and biomolecular engineering.

[31]  D. Mooney,et al.  Mechanical forces direct stem cell behaviour in development and regeneration , 2017, Nature Reviews Molecular Cell Biology.

[32]  S. Djurovic,et al.  Comparison of nonviral transfection and adeno-associated viral transduction on cardiomyocytes , 2004, Molecular biotechnology.

[33]  T. Ichisaka,et al.  Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors , 2007, Cell.

[34]  H. Uludaǧ,et al.  Cellular uptake pathways of lipid-modified cationic polymers in gene delivery to primary cells. , 2012, Biomaterials.

[35]  M. S. Kallos,et al.  Large-scale production of murine embryonic stem cell-derived osteoblasts and chondrocytes on microcarriers in serum-free media. , 2011, Biomaterials.

[36]  M. S. Kallos,et al.  Inter‐microcarrier transfer and phenotypic stability of stem cell‐derived Schwann cells in stirred suspension bioreactor culture , 2016, Biotechnology and bioengineering.

[37]  Gordon Keller,et al.  Differentiation of Embryonic Stem Cells to Clinically Relevant Populations: Lessons from Embryonic Development , 2008, Cell.