Cells were stained with CD3-APC, CD4-FITC, CD8-APC Vio770, CD14-PE Vio770, and CD45-Vioblue (Miltenyi Biotec). To assess the efficiency of transduction, CAR-T cells were stained with CD-19 Biotin and anti-Biotin PE (Miltenyi Biotec). Viability was tested by using 7-AAD (Miltenyi Biotec). Phenotype was determined with CD45RA-APC (HI100) and CCR7-BV421 (2-L1-A RUO) from BD Pharmingen. Cells were acquired on a MACsQuant cytometer (Miltenyi Biotec) and analyzed with MACsQuantify Analysis Software (Miltenyi Biotec).
Large-Scale GMP-Like CAR-T Cell Manufacturing
Cells were stained with CD3-APC, CD4-FITC, CD8-APC Vio770, CD14-PE Vio770, and CD45-Vioblue (Miltenyi Biotec). To assess the efficiency of transduction, CAR-T cells were stained with CD-19 Biotin and anti-Biotin PE (Miltenyi Biotec). Viability was tested by using 7-AAD (Miltenyi Biotec). Phenotype was determined with CD45RA-APC (HI100) and CCR7-BV421 (2-L1-A RUO) from BD Pharmingen. Cells were acquired on a MACsQuant cytometer (Miltenyi Biotec) and analyzed with MACsQuantify Analysis Software (Miltenyi Biotec).
Corresponding Organization : Universidad de Granada
Other organizations : Instituto Maimónides de Investigación Biomédica de Córdoba, University of Córdoba, Hospital Clínic de Barcelona, Instituto de Investigación Biosanitaria de Granada
Variable analysis
- Transduction with AWARI-LVs (MOI = 5)
- Efficiency of transduction (assessed by CD19 Biotin and anti-Biotin PE staining)
- Viability (tested by 7-AAD staining)
- Phenotype (determined by CD45RA-APC and CCR7-BV421 staining)
- Culturing CD4 and CD8 cells with IL-7 and IL-15
- Activating cells with αCD3 and αCD28 GMP T cell TransAct
- Culturing cells in TexMACs GMP medium containing GMP-grade IL-15 and IL-7
- Collecting final product with 100 mL of NaCl 0.9% + 0.5% human serum albumin (HSA)
- Staining cells with CD3-APC, CD4-FITC, CD8-APC Vio770, CD14-PE Vio770, and CD45-Vioblue
Annotations
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