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Antibody‐Based CAR T Cells Produced by Lentiviral Transduction

Sabrina Prommersberger, Michael Hudecek, Thomas Nerreter

2020Current Protocols in Immunology27 citationsDOIOpen Access PDF

Abstract

One promising approach to treat hematologic malignancies is the usage of patient-derived CAR T cells. There are continuous efforts to improve the function of these cells, to optimize their receptor, and to use them for the treatment of additional types of cancer and especially solid tumors. In this protocol, an easy and reliable approach for CAR T cell generation is described. T cells are first isolated from peripheral blood (here: leukoreduction system chambers) and afterwards activated for one day with anti-CD3/CD28 Dynabeads. The gene transfer is performed by lentiviral transduction and gene transfer rate can be verified by flowcytometric analysis. Six days after transduction, the stimulatory Dynabeads are removed. T cells are cultured in interleukin-2 conditioned medium for several days for expansion. There is an option to expand CAR T cells further by co-incubation with irradiated, antigen-expressing feeder cell lines. The CAR T cells are ready to use after 10 (without feeder cell expansion) to 24 days (with feeder cell expansion). © 2020 The Authors. Basic Protocol: Generation of CAR T cells by lentiviral transduction.

Topics & Concepts

LeukoreductionTransduction (biophysics)CD28Chimeric antigen receptorT cellCell biologyCD3BiologyMolecular biologyAntigenImmunologyChemistryImmune systemCD8BiochemistryBlood transfusionCAR-T cell therapy researchVirus-based gene therapy researchViral Infectious Diseases and Gene Expression in Insects
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