Decisional tools for cost-effective bioprocess design for cell therapies and patient-specific drug discovery tools

A specific challenge to the translation of cell therapies and stem-cell derived products is the ability to develop and manufacture such products in a cost-effective, scalable and robust manner. To this end, this thesis investigates the creation and application of a set of computational tools designed to aid bioprocess design decisions for cell therapy and stem-cell derived research products. The decision-support tools comprise advanced bioprocess economics models with databases tailored to cellular products. These are linked to Monte Carlo simulation for uncertainty analysis and techniques to identify optimal bioprocess designs that include brute-force search algorithms, an evolutionary algorithm, and multi-attribute decision making analysis. A trio of industrially-relevant case studies is presented within this thesis, along with an additional study included in the appendices of this work, in order to demonstrate the applicability of the decisional tools to bioprocess design for different cell therapies (allogeneic, human embryonic stem cell-derived retinal pigment epithelial (RPE) cells for macular degeneration, allogeneic CAR-T cells for oncology) and induced pluripotent stem cells (iPSCs) for drug discovery applications. Questions tackled included manual versus automated production, costeffective inflection points of planar vs microcarrier-based bioprocess strategies, and the identification optimal process technologies for an allogeneic CAR-T cell therapy based on both qualitative and quantitative attributes. The analyses highlighted key bioprocess economic drivers and process bottlenecks. Furthermore, the Monte Carlo simulation technique was used in order to capture the effects of the inherent uncertainty associated with cell therapy bioprocessing on manufacturing costs and process throughputs. Future process improvements required to create financially feasible bioprocesses were also identified. This thesis presents the application of a series of decisional tools to bioprocess design problems and demonstrates how they can facilitate informed decisions regarding cost-effective process design in the cell therapy sector.

[1]  Suzanne S. Farid,et al.  Process Economic Drivers in Industrial Monoclonal Antibody Manufacture , 2008 .

[2]  Gideon Rechavi,et al.  Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cells. , 2009, Cell stem cell.

[3]  Devyn M. Smith,et al.  Assessing commercial opportunities for autologous and allogeneic cell-based products. , 2012, Regenerative medicine.

[4]  R. Stewart,et al.  Human Induced Pluripotent Stem Cells Free of Vector and Transgene Sequences , 2009, Science.

[5]  Suzanne S Farid,et al.  Decision‐Support Tool for Assessing Biomanufacturing Strategies under Uncertainty: Stainless Steel versus Disposable Equipment for Clinical Trial Material Preparation , 2008, Biotechnology progress.

[6]  Nasir Malik,et al.  Assessing iPSC reprogramming methods for their suitability in translational medicine , 2012, Journal of cellular biochemistry.

[7]  Ashutosh Kumar Singh,et al.  A microparticle approach to morphogen delivery within pluripotent stem cell aggregates. , 2013, Biomaterials.

[8]  M. Choolani,et al.  Microcarrier Culture for Efficient Expansion and Osteogenic Differentiation of Human Fetal Mesenchymal Stem Cells , 2013, BioResearch open access.

[9]  Catarina Brito,et al.  Process engineering of human pluripotent stem cells for clinical application. , 2012, Trends in biotechnology.

[10]  K. Cornetta,et al.  Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction. , 1990, The New England journal of medicine.

[11]  S. Engle,et al.  Small Molecule Screening in Human Induced Pluripotent Stem Cell-derived Terminal Cell Types* , 2013, The Journal of Biological Chemistry.

[12]  Rudolf Jaenisch,et al.  Parkinson's Disease Patient-Derived Induced Pluripotent Stem Cells Free of Viral Reprogramming Factors , 2009, Cell.

[13]  R. Zweigerdt The art of cobbling a running pump--will human embryonic stem cells mend broken hearts? , 2007, Seminars in cell & developmental biology.

[14]  K. Chien,et al.  Long-term self-renewal of human pluripotent stem cells on human recombinant laminin-511 , 2010, Nature Biotechnology.

[15]  Robert Zweigerdt,et al.  Suspension culture of human pluripotent stem cells in controlled, stirred bioreactors. , 2012, Tissue engineering. Part C, Methods.

[16]  Richard Allmendinger,et al.  Tuning evolutionary search for closed-loop optimization , 2012 .

[17]  Wanguo Wei,et al.  Chemical strategies for stem cell biology and regenerative medicine. , 2011, Annual review of biomedical engineering.

[18]  Naoki Nishishita,et al.  Efficient generation of transgene-free human induced pluripotent stem cells (iPSCs) by temperature-sensitive Sendai virus vectors , 2011, Proceedings of the National Academy of Sciences.

[19]  C. Mason,et al.  The global cell therapy industry continues to rise during the second and third quarters of 2012. , 2012, Cell stem cell.

[20]  C. Kerr,et al.  Pluripotent stem cells from germ cells. , 2006, Methods in enzymology.

[21]  Ofer Binah,et al.  Cardiomyocytes derived from human pluripotent stem cells for drug screening. , 2012, Pharmacology & therapeutics.

[22]  Y. Fujita,et al.  Regenerative medicine legislation in Japan for fast provision of cell therapy products , 2016, Clinical pharmacology and therapeutics.

[23]  D. Gilham,et al.  Targeted immunotherapy of cancer with CAR T cells: achievements and challenges , 2012, Cancer Immunology, Immunotherapy.

[24]  D. Powell,et al.  Efficient clinical-scale enrichment of lymphocytes for use in adoptive immunotherapy using a modified counterflow centrifugal elutriation program. , 2009, Cytotherapy.

[25]  S. Reuveny,et al.  Critical microcarrier properties affecting the expansion of undifferentiated human embryonic stem cells. , 2011, Stem cell research.

[26]  S. Bhattacharya,et al.  Hypoxia enhances the generation of retinal progenitor cells from human induced pluripotent and embryonic stem cells. , 2012, Stem cells and development.

[27]  Vincent C. Chen,et al.  Scalable GMP compliant suspension culture system for human ES cells. , 2012, Stem cell research.

[28]  Farlan S. Veraitch,et al.  Bioprocessing Challenges Associated with the Purification of Cellular Therapies , 2014 .

[29]  Chris Mason,et al.  The impact of manual processing on the expansion and directed differentiation of embryonic stem cells , 2008, Biotechnology and bioengineering.

[30]  S. Reuveny,et al.  3D microcarrier system for efficient differentiation of human pluripotent stem cells into hematopoietic cells without feeders and serum [corrected]. , 2013, Regenerative medicine.

[31]  Praveen Shukla,et al.  Engineered heart tissues and induced pluripotent stem cells: Macro- and microstructures for disease modeling, drug screening, and translational studies. , 2016, Advanced drug delivery reviews.

[32]  S. Olivares,et al.  Manufacture of Clinical-Grade CD19-Specific T Cells Stably Expressing Chimeric Antigen Receptor Using Sleeping Beauty System and Artificial Antigen Presenting Cells , 2013, PloS one.

[33]  Mark S. Humayun,et al.  Stem cell based therapies for age-related macular degeneration: The promises and the challenges , 2015, Progress in Retinal and Eye Research.

[34]  D. Ilic,et al.  Human embryonic and induced pluripotent stem cells in clinical trials. , 2015, British medical bulletin.

[35]  S. Reuveny,et al.  Long-term microcarrier suspension cultures of human embryonic stem cells. , 2009, Stem cell research.

[36]  Xuan Yuan,et al.  A Universal System for Highly Efficient Cardiac Differentiation of Human Induced Pluripotent Stem Cells That Eliminates Interline Variability , 2011, PloS one.

[37]  Hossein Baharvand,et al.  Technological progress and challenges towards cGMP manufacturing of human pluripotent stem cells based therapeutic products for allogeneic and autologous cell therapies. , 2013, Biotechnology advances.

[38]  Jason Hipp,et al.  Derivation and comparative assessment of retinal pigment epithelium from human embryonic stem cells using transcriptomics. , 2004, Cloning and stem cells.

[39]  Sean P. Palecek,et al.  Functional Cardiomyocytes Derived From Human Induced Pluripotent Stem Cells , 2009, Circulation research.

[40]  Gareth J.S. Jenkins,et al.  Potential toxicity of superparamagnetic iron oxide nanoparticles (SPION) , 2010, Nano reviews.

[41]  P. Czermak,et al.  Expansion and Harvesting of hMSC-TERT , 2007, The open biomedical engineering journal.

[42]  Maria Margarida Diogo,et al.  Stem cell cultivation in bioreactors. , 2011, Biotechnology advances.

[43]  Masayo Takahashi,et al.  Design of a Tumorigenicity Test for Induced Pluripotent Stem Cell (iPSC)-Derived Cell Products , 2015, Journal of clinical medicine.

[44]  K. Woltjen,et al.  Virus free induction of pluripotency and subsequent excision of reprogramming factors , 2009, Nature.

[45]  S. Reuveny,et al.  Inhibition of ROCK-myosin II signaling pathway enables culturing of human pluripotent stem cells on microcarriers without extracellular matrix coating. , 2014, Tissue engineering. Part C, Methods.

[46]  S. Agathos,et al.  Process engineering of stem cell metabolism for large scale expansion and differentiation in bioreactors , 2014 .

[47]  Dirk Strunk,et al.  Two steps to functional mesenchymal stromal cells for clinical application , 2007, Transfusion.

[48]  N. Medcalf Centralized or decentralized manufacturing? Key business model considerations for cell therapies , 2016 .

[49]  A. Hampl,et al.  Comparative study of mouse and human feeder cells for human embryonic stem cells. , 2008, The International journal of developmental biology.

[50]  Ronald A. Li,et al.  A simple, cost-effective but highly efficient system for deriving ventricular cardiomyocytes from human pluripotent stem cells. , 2014, Stem cells and development.

[51]  N. Benvenisty,et al.  Human Embryonic Stem Cells and Their Differentiated Derivatives Are Less Susceptible to Immune Rejection Than Adult Cells , 2006, Stem cells.

[52]  S. Rosenberg,et al.  Clinical scale rapid expansion of lymphocytes for adoptive cell transfer therapy in the WAVE® bioreactor , 2012, Journal of Translational Medicine.

[53]  Itzhak Mizrahi,et al.  Scalable production of cardiomyocytes derived from c-Myc free induced pluripotent stem cells. , 2011, Tissue engineering. Part A.

[54]  Daniel G. Anderson,et al.  Ex Vivo Cytosolic Delivery of Functional Macromolecules to Immune Cells , 2015, PloS one.

[55]  S. Bauer,et al.  Quantitative approaches to detect donor and passage differences in adipogenic potential and clonogenicity in human bone marrow-derived mesenchymal stem cells. , 2012, Tissue engineering. Part C, Methods.

[56]  Shinsuke Yuasa,et al.  Generation of induced pluripotent stem cells from human terminally differentiated circulating T cells. , 2010, Cell stem cell.

[57]  P. Zandstra,et al.  High density continuous production of murine pluripotent cells in an acoustic perfused bioreactor at different oxygen concentrations. , 2013, Biotechnology and bioengineering.

[58]  Andre Choo,et al.  Scalable platform for human embryonic stem cell differentiation to cardiomyocytes in suspended microcarrier cultures. , 2010, Tissue engineering. Part C, Methods.

[59]  S. Ylä-Herttuala Glybera's second act: the curtain rises on the high cost of therapy. , 2015, Molecular therapy : the journal of the American Society of Gene Therapy.

[60]  Michel Sadelain,et al.  Safety and persistence of adoptively transferred autologous CD19-targeted T cells in patients with relapsed or chemotherapy refractory B-cell leukemias. , 2011, Blood.

[61]  Lyndon da Cruz,et al.  Development of human embryonic stem cell therapies for age-related macular degeneration , 2013, Trends in Neurosciences.

[62]  Masayuki Yamato,et al.  Temperature-responsive poly(N-isopropylacrylamide)-grafted microcarriers for large-scale non-invasive harvest of anchorage-dependent cells. , 2012, Biomaterials.

[63]  N J Titchener-Hooker,et al.  Economic comparison between conventional and disposables-based technology for the production of biopharmaceuticals. , 2001, Biotechnology and bioengineering.

[64]  S. Gerecht,et al.  Scalable expansion of human induced pluripotent stem cells in the defined xeno-free E8 medium under adherent and suspension culture conditions. , 2013, Stem cell research.

[65]  L. Muul,et al.  Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[66]  Mayasari Lim,et al.  Stem cell bioprocessing: fundamentals and principles , 2009, Journal of The Royal Society Interface.

[67]  Thomas Scheper,et al.  Long term expansion of undifferentiated human iPS and ES cells in suspension culture using a defined medium. , 2010, Stem cell research.

[68]  S. Reuveny,et al.  Agitation can induce differentiation of human pluripotent stem cells in microcarrier cultures. , 2011, Tissue engineering. Part C, Methods.

[69]  B. Strulovici,et al.  Induced pluripotent stem cells — opportunities for disease modelling and drug discovery , 2011, Nature Reviews Drug Discovery.

[70]  S. Schwartz,et al.  Embryonic stem cell trials for macular degeneration: a preliminary report , 2012, The Lancet.

[71]  C. Mason,et al.  A brief definition of regenerative medicine. , 2008, Regenerative medicine.

[72]  C. McIntyre,et al.  Fluorescence-Activated Cell Sorting for CGMP Processing of Therapeutic Cells , 2010 .

[73]  J. Clemente,et al.  Improving expansion of pluripotent human embryonic stem cells in perfused bioreactors through oxygen control. , 2010, Journal of biotechnology.

[74]  M. Hervy,et al.  Long Term Expansion of Bone Marrow-Derived hMSCs on Novel Synthetic Microcarriers in Xeno-Free, Defined Conditions , 2014, PloS one.

[75]  W. Khan,et al.  Optimising Human Mesenchymal Stem Cell Numbers for Clinical Application: A Literature Review , 2012, Stem cells international.

[76]  Hanns-Ulrich Marschall,et al.  Mesenchymal Stem Cells for Treatment of Therapy-Resistant Graft-versus-Host Disease , 2006, Transplantation.

[77]  H. Baharvand,et al.  Bioprocess development for mass production of size-controlled human pluripotent stem cell aggregates in stirred suspension bioreactor. , 2012, Tissue engineering. Part C, Methods.

[78]  M. Pistello,et al.  Viral vectors: a look back and ahead on gene transfer technology. , 2013, The new microbiologica.

[79]  J. Spicer,et al.  Design of a Phase I Clinical Trial to evaluate intra-tumoral delivery of ErbB-targeted CAR T-cells in locally advanced or recurrent Head and Neck Cancer , 2013 .

[80]  Andrew Buchanan,et al.  Clinical development of advanced therapy medicinal products in Europe: evidence that regulators must be proactive. , 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

[81]  Sunil Chhatre,et al.  A prototype software methodology for the rapid evaluation of biomanufacturing process options , 2007, Biotechnology and applied biochemistry.

[82]  Shu-Ching Hsu,et al.  Internalized antigens must be removed to prepare hypoimmunogenic mesenchymal stem cells for cell and gene therapy. , 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

[83]  Michael Hay,et al.  Clinical development success rates for investigational drugs , 2014, Nature Biotechnology.

[84]  S. Rosenberg,et al.  Clinical-scale Lentiviral Vector Transduction of PBL for TCR Gene Therapy and Potential for Expression in Less-differentiated Cells , 2008, Journal of immunotherapy.

[85]  J. Hyllner,et al.  Cell-based therapy technology classifications and translational challenges , 2015, Philosophical Transactions of the Royal Society B: Biological Sciences.

[86]  J. Mineno,et al.  An Efficient Large-Scale Retroviral Transduction Method Involving Preloading the Vector into a RetroNectin-Coated Bag with Low-Temperature Shaking , 2014, PloS one.

[87]  Bo Kara,et al.  Expansion, harvest and cryopreservation of human mesenchymal stem cells in a serum‐free microcarrier process , 2015, Biotechnology and bioengineering.

[88]  A. Bishop,et al.  Embryonic stem cells , 2004, Cell proliferation.

[89]  N. Ashammakhi,et al.  Immunomodulatory effect of mesenchymal stromal cells: possible mechanisms. , 2008, Regenerative medicine.

[90]  R. Seetharam,et al.  Serum‐free media for the production of human mesenchymal stromal cells: a review , 2013, Cell proliferation.

[91]  David A. Williams,et al.  Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells , 1996, Nature Medicine.

[92]  Sally Hassan,et al.  Allogeneic cell therapy bioprocess economics and optimization: downstream processing decisions. , 2015, Regenerative medicine.

[93]  Hao Liu,et al.  Virus-specific T cells engineered to coexpress tumor-specific receptors: persistence and antitumor activity in individuals with neuroblastoma , 2008, Nature Medicine.

[94]  A. Radbruch,et al.  Small but mighty: How the MACS®‐technology based on nanosized superparamagnetic particles has helped to analyze the immune system within the last 20 years , 2010, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[95]  Chong Cheng,et al.  Facile engineering of xeno-free microcarriers for the scalable cultivation of human pluripotent stem cells in stirred suspension. , 2013, Tissue engineering. Part A.

[96]  Suzanne Farid A decision-support tool for simulating the process and business perspectives of biopharmaceutical manufacture. , 2002 .

[97]  W. Wilson,et al.  B-cell depletion and remissions of malignancy along with cytokine-associated toxicity in a clinical trial of anti-CD19 chimeric-antigen-receptor-transduced T cells. , 2012, Blood.

[98]  E. Jaffee,et al.  Lentivirus-mediated gene transfer and expression in established human tumor antigen-specific cytotoxic T cells and primary unstimulated T cells. , 2003, Human gene therapy.

[99]  C. Hewitt,et al.  Systematic microcarrier screening and agitated culture conditions improves human mesenchymal stem cell yield in bioreactors , 2016, Biotechnology journal.

[100]  C. Mason,et al.  Quantities of cells used for regenerative medicine and some implications for clinicians and bioprocessors. , 2009, Regenerative medicine.

[101]  Suzanne S Farid,et al.  Fed‐batch and perfusion culture processes: Economic, environmental, and operational feasibility under uncertainty , 2013, Biotechnology and bioengineering.

[102]  Suzanne S Farid,et al.  A computer‐aided approach to compare the production economics of fed‐batch and perfusion culture under uncertainty , 2006, Biotechnology and bioengineering.

[103]  F. Cosset,et al.  Lentiviral vectors pseudotyped with a modified RD114 envelope glycoprotein show increased stability in sera and augmented transduction of primary lymphocytes and CD34+ cells derived from human and nonhuman primates. , 2002, Blood.

[104]  A. Stonier,et al.  A dynamic decision support tool for use in the design of bio-manufacturing facilities and processes , 2013 .

[105]  George Q. Daley,et al.  Reprogramming of human somatic cells to pluripotency with defined factors , 2008, Nature.

[106]  Robert J. Thomas,et al.  Expansion of human mesenchymal stem cells on microcarriers , 2011, Biotechnology Letters.

[107]  Peter W. Zandstra,et al.  Rational bioprocess design for human pluripotent stem cell expansion and endoderm differentiation based on cellular dynamics. , 2012, Biotechnology and bioengineering.

[108]  S. Rehen,et al.  Xeno-free production of human embryonic stem cells in stirred microcarrier systems using a novel animal/human-component-free medium. , 2013, Tissue engineering. Part C, Methods.

[109]  J. Gimble,et al.  A xenogeneic‐free bioreactor system for the clinical‐scale expansion of human mesenchymal stem/stromal cells , 2014, Biotechnology and bioengineering.

[110]  A. Reinisch,et al.  Rapid large-scale expansion of functional mesenchymal stem cells from unmanipulated bone marrow without animal serum. , 2008, Tissue engineering. Part C, Methods.

[111]  George Q. Daley,et al.  Biomechanical forces promote embryonic haematopoiesis , 2009, Nature.

[112]  Z. Eshhar,et al.  Expression of immunoglobulin-T-cell receptor chimeric molecules as functional receptors with antibody-type specificity. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[113]  P. Kefalas,et al.  Reimbursement of licensed cell and gene therapies across the major European healthcare markets , 2015, Journal of market access & health policy.

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

[115]  Karen Coopman,et al.  Large-scale expansion and exploitation of pluripotent stem cells for regenerative medicine purposes: beyond the T flask. , 2012, Regenerative medicine.

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

[117]  T. Braun,et al.  Cardiomyocyte production in mass suspension culture: Embryonic stem cells as a source for great amounts of functional cardiomyocytes , 2005 .

[118]  I. Kola,et al.  Can the pharmaceutical industry reduce attrition rates? , 2004, Nature Reviews Drug Discovery.

[119]  M. Tomishima,et al.  Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling , 2009, Nature Biotechnology.

[120]  Wenbo Zhou,et al.  Adenoviral Gene Delivery Can Reprogram Human Fibroblasts to Induced Pluripotent Stem Cells , 2009, Stem cells.

[121]  P. Andrade,et al.  Maximizing the ex vivo expansion of human mesenchymal stem cells using a microcarrier-based stirred culture system. , 2010, Journal of biotechnology.

[122]  Elisa Cimetta,et al.  Micro-bioreactor arrays for controlling cellular environments: design principles for human embryonic stem cell applications. , 2009, Methods.

[123]  S. Rehen,et al.  Successful scale-up of human embryonic stem cell production in a stirred microcarrier culture system. , 2009, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

[124]  Jon A. Rowley,et al.  Meeting Lot-Size Challenges of Manufacturing Adherent Cells for Therapy , 2012 .

[125]  Hu Li,et al.  Cellular Reprogramming: A New Technology Frontier in Pharmaceutical Research , 2011, Pharmaceutical Research.

[126]  G. Daley,et al.  The promise of induced pluripotent stem cells in research and therapy , 2012, Nature.

[127]  Anne Lindgren,et al.  Directed Differentiation of Human‐Induced Pluripotent Stem Cells Generates Active Motor Neurons , 2009, Stem cells.

[128]  Janet Woodcock,et al.  Expediting drug development--the FDA's new "breakthrough therapy" designation. , 2013, The New England journal of medicine.

[129]  DiekmannUlf,et al.  A reliable and efficient protocol for human pluripotent stem cell differentiation into the definitive endoderm based on dispersed single cells. , 2015 .

[130]  K. Krause,et al.  Generation and Applications of Human Pluripotent Stem Cells Induced into Neural Lineages and Neural Tissues , 2012, Front. Physio..

[131]  John E. Hambor,et al.  Bioreactor Design and Bioprocess Controls for Industrialized Cell Processing Bioengineering Strategies and Platform Technologies , 2012 .

[132]  J. Lahann,et al.  EMBRYONIC STEM CELLS/INDUCED PLURIPOTENT STEM CELLS Concise Review: The Evolution of Human Pluripotent Stem Cell Culture: From Feeder Cells to Synthetic Coatings , 2012 .

[133]  Shuibing Chen,et al.  Pluripotent stem cell-derived pancreatic β-cells: potential for regenerative medicine in diabetes. , 2012, Regenerative medicine.

[134]  Mudit Gupta,et al.  Highly efficient miRNA-mediated reprogramming of mouse and human somatic cells to pluripotency. , 2011, Cell stem cell.

[135]  N. Kalogerakis,et al.  Development of the optimal inoculation conditions for microcarrier cultures , 1992, Biotechnology and bioengineering.