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This article details the manufacturing process for chimeric antigen receptor T cells for clinical use, specifically using an automated cell processor capable of performing viral transduction and cultivation of T cells. We provide recommendations and describe pitfalls that should be considered during the process development and implementation of an early-phase clinical trial.
Chimeric antigen receptor (CAR)-T cells represent a promising immunotherapeutic approach for the treatment of various malignant and non-malignant diseases. CAR-T cells are genetically modified T cells that express a chimeric protein that recognizes and binds to a cell surface target, resulting in the killing of the target cell. Traditional CAR-T cell manufacturing methods are labor-intensive, expensive, and may carry the risk of contamination. The CliniMACS Prodigy, an automated cell processor, allows for manufacturing cell therapy products at a clinical scale in a closed system, minimizing the risk of contamination. Processing occurs semi-automatically under the control of a computer and thus minimizes human involvement in the process, which saves time and reduces variability and errors.
This manuscript and video describes the T cell transduction (TCT) process for manufacturing CAR-T cells using this processor. The TCT process involves CD4+/CD8+ T cell enrichment, activation, transduction with a viral vector, expansion, and harvest. Using the Activity Matrix, a functionality that allows ordering and timing of these steps, the TCT process can be customized extensively. We provide a walk-through of CAR-T cell manufacturing in compliance with current Good Manufacturing Practice (cGMP) and discuss required release testing and preclinical experiments that will support an Investigational New Drug (IND) application. We demonstrate the feasibility and discuss the advantages and disadvantages of using a semi-automatic process for clinical CAR-T cell manufacturing. Finally, we describe an ongoing investigator-initiated clinical trial that targets pediatric B-cell malignancies [NCT05480449] as an example of how this manufacturing process can be applied in a clinical setting.
Adoptive transfer of T cells engineered to express a chimeric antigen receptor (CAR) has shown remarkable efficacy in treating patients with refractory B-cell malignancies1,2,3,4,5. However, the traditional manufacturing methods for CAR-T cells are labor-intensive, time-consuming, and require highly trained technicians to carry out highly specialized steps. For example, the traditional manufacturing process of an autologous CAR-T cell product involves density gradient centrifugation, elutriation or mag....
All research was performed in compliance with institutional guidelines with approval by the hospital's Institutional Review Board (IRB), and all subjects have provided informed consent for publication of the data collected within the context of the trial.
NOTE: The first section of the Protocol provides a high-level overview of the CAR-T manufacturing process. The remaining sections provide the step-by-step instructions. The protocol describes the workflow using TCT software version 1.4, which is the .......
Results from the initial three CAR-T manufacturing runs of the NCT05480449 trial are presented below in Table 3. The starting material, vector, culture cytokines, and AB serum concentrations were kept consistent for each run. Products were harvested on day 7 or 8. The average daily cell growth was 46% (increase in total cell count), indicating that the TCT process was effective in promoting cell expansion. These results suggest that the processor can produce consistent and reproducible CAR-T cell product.......
CAR-T cell therapy has emerged as a promising treatment approach for B-cell and other malignancies. However, traditional CAR-T cell manufacturing methods have several limitations, such as high cost, labor-intensive production, and open steps that increase the risk of contamination. Recently, several semi-automated platforms, including the Miltenyi CliniMACS Prodigy (the "processor"), have emerged to address these limitations. The T cell transduction (TCT) process, integrated into the processor described in this m.......
The authors would like to acknowledge the contributions of several individuals and organizations to this work. The Cell and Gene Therapy Laboratory and the Penn Translational and Correlative Studies Laboratory provided valuable assistance with process development and preparation for IND submissions. Melissa Varghese and Amanda DiNofia contributed to the process development and preparation for IND submissions that underly this manuscript. This work was supported by an Acceleration Grant of the Cell and Gene Therapy Collaborative of the Children's Hospital of Philadelphia. The authors would also like to thank Miltenyi Biotec for their technical and research sup....
Name | Company | Catalog Number | Comments |
12 x 75 borosilicate tubes | Charles River | TL1000 | |
20 mL Reagent Bag | Miltenyi Biotec | 170-076-631 | |
50 mL Conical Tube | Fisher | 05-539-10 | |
150 mL Transfer Set | Fenwal | 4R2001 | |
2,000 mL Transfer Set | Fenwal | 4R2041 | |
7AAD | Fisher Scientific | BDB559925 | |
Alcohol Prep | Tyco/Healthcare | ||
Bag Access | Medline | 2300E-0500 | |
CD19 APC-Vio770 REAfinity | Miltenyi Biotec | 130-113-643 | |
CD19 CAR Detection Reagent Biotin | Miltenyi Biotec | 130-129-550 | |
CD19 PE | BD | 555413 | |
CD3 APC | BD | 340440 | |
CD4 VioBright FITC REAfinity | Miltenyi Biotec | 130-113-229 | |
CD45 VioBlue REAfinity | Miltenyi Biotec | 130-110-637 | |
CD8 APC-Vio770 REAfinity | Miltenyi Biotec | 130-110-681 | |
Cellometer Reference Beads 10um | Nexcelom | B10-02-020 | |
Cellometer Reference Beads 15um | Nexcelom | B15-02-010 | |
Cellometer Reference Beads 5um | Nexcelom | B05-02-050 | |
Cellometer Slides | Nexcelom | CHT4-SD100-002 | |
CliniMACS CD4 GMP MicroBeads | Miltenyi Biotec | 276-01 | The CD4 reagent |
CliniMACS CD8 GMP MicroBeads | Miltenyi Biotec | 275-01 | The CD8 reagent |
CliniMACS PBS/EDTA Buffer | Miltenyi Biotec | 130-021-201 | The buffer |
DMSO | Origen | CP-10 | |
Freezing Bag 50 mL | Miltenyi Biotec | 200-074-400 | |
Freezing Vial, 1.8 mL | Nunc | 12565171N | |
Freezing Vial, 4.5 mL | Nunc | 12565161N | |
Human AB serum | Valley Biomedical | Sterile filtered, heat inactivated | |
Human Serum Albumin 25% | Grifols | 68516-5216-1 | |
Human Serum Albumin 5% | Grifols | 68516-5214-1 | |
MACS GMP Recombinant Human IL-2 | Miltenyi Biotec | 170-076-148 | The cytokines |
MACS GMP T Cell TransAct | Miltenyi Biotec | 200-076-202 | The activation reagent |
MycoSeq Mycoplasma Detection Kit | Life Technologies | 4460623 | |
Needles, Hypodermic 14G | Medline | SWD200573 | |
Needles, SlideSafe 18G | BD | B-D305918 | |
Pipet tips, 2-200 μL, individually wrapped | Eppendorf | 022492209 | |
Pipet tips, 50-1000 μL, individually wrapped | Eppendorf | 022492225 | |
Pipets 10 mL | Fisher | 13-678-27F | |
Pipets 25 mL | Fisher | 13-675-30 | |
Pipets 5 mL | Fisher | 13-678-27E | |
Plasmalyte-A | Baxter | 2B2544X | The electrolyte solution |
Prodigy TS520 Tubing Set | Miltenyi Biotec | 170-076- 600 | The tubing set |
Sterile Field | Medline | NON21001 | |
Streptavidin PE-Vio770 | Miltenyi Biotec | 130-106-793 | |
Syringe 1 mL | BD | 309628 | |
Syringe 10 mL | BD | 302995 | |
Syringe 3 mL | BD | 309657 | |
Syringe 30 mL | BD | 302832 | |
Syringe 50 mL | BD | 309653 | |
TexMACS GMP Medium | Miltenyi Biotec | 170-076-306 | The medium |
Triple Sampling Adapter | Miltenyi Biotec | 170-076-609 | |
Viral Vector | CHOP Clinical Vector Core | huCART19 | |
Equipment | |||
Biological Safety Cabinet | The Baker Co | ||
Cellometer Auto 2000 | Nexcelom | ||
CliniMACS Prodigy | Miltenyi Biotec | 200-075-301 | The processor |
Controlled Rate Freezer | Planer/Kryosave | ||
Endosafe nexgen-PTS150K | Charles River | ||
Mettler Balance | Mettler | ||
Refrigerated Centrifuge | Thermo Fisher | ||
Refrigerated Centrifuge | Fisher Sci | ||
SCD Sterile Tubing Welder | Terumo | ||
Sebra Tube Sealer | Sebra | ||
Varitherm | Barkey | The dry thaw device | |
XN-330 Hematology Analyzer | Sysmex |
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