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Image Search Results
Journal: Molecular Therapy
Article Title: CRISPR-Cas9-Edited Tacrolimus-Resistant Antiviral T Cells for Advanced Adoptive Immunotherapy in Transplant Recipients
doi: 10.1016/j.ymthe.2020.09.011
Figure Lengend Snippet: Protocol Outline for a GMP-Compatible Approach to Induce Tacrolimus Resistance in a CMV-Specific TCP Using Vector-Free CRISPR-Cas9 Technology (A) Individual steps of the production process. (B) Representative purities of CMV-specific IFNγ-producing T cells pre - and post-enrichment from PBMCs. (C) Calculated KO efficiency of FKBP12 in CMV-specific TCPs. (D) Expansion rates of electroporated CMV-specific TCPs normalized to expansion rates of the unmodified control from day 7 to day 21 (following electroporation). (E) Different immunosuppressants used for functional analyses and their affected adaptor proteins or receptors and pathways. Classic triple IS consists of a CNI, prednisolone, and MPA.
Article Snippet: 2.5 million antiviral T cells were electroporated on day 7 after isolation using the Amaxa P3 Primary Cell 4D-Nucleofector X Kit L and the Amaxa-Nucleofector-4D (Lonza, program CO-115) to transfer RNP complexes of 30 μg of
Techniques: Plasmid Preparation, CRISPR, Electroporation, Functional Assay
Journal: Molecular Therapy
Article Title: CRISPR-Cas9-Edited Tacrolimus-Resistant Antiviral T Cells for Advanced Adoptive Immunotherapy in Transplant Recipients
doi: 10.1016/j.ymthe.2020.09.011
Figure Lengend Snippet: Cas9 Protein Is Undetectable in FKBP12 KO CMV TCPs Shown are proportions of edited T cells stained for Cas9 protein at different time points after electroporation.
Article Snippet: 2.5 million antiviral T cells were electroporated on day 7 after isolation using the Amaxa P3 Primary Cell 4D-Nucleofector X Kit L and the Amaxa-Nucleofector-4D (Lonza, program CO-115) to transfer RNP complexes of 30 μg of
Techniques: Staining, Electroporation