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Chimeric antigen receptor (CAR)+ T cell selection method affects transgene efficacy
  1. David Rushworth1,2,
  2. Tiejuan Mi1,
  3. Simon Olivares1,
  4. Rosa Santana Carrero3,
  5. Ge Yang1,
  6. Amer Najjar1 and
  7. Laurence Cooper1,2
  1. Aff1 grid.240145.60000000122914776PediatricsMD Anderson Cancer Center Houston TX USA
  2. Aff2 grid.267308.80000000092062401Graduate School of Biomedical SciencesUT Houston Health Science Center Houston TX USA
  3. Aff3 grid.412177.60000000404621680Medical SciencesUniversity of Puerto Rico School of Medicine San Juan US Minor Outlying Islands

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Meeting abstracts

The use of CAR+ T cells for the treatment of cancer is growing as multiple centers participate in Phase I/II clinical trials. Prior studies of CAR-dependent T cell effector function evaluated CAR design on T-cell responses in vitro and in vivo. Our study assesses the effect ex vivo co-stimulation imparts on in vitro and in vivo effector function of CAR+ T cells. In this study, the well characterized CD19-specific 2nd generation CAR, signaling through CD28 and CD3-ζ endodomains, was expressed in donor T cells. Non-virally transformed T cells, induced to genomically integrate CAR by Sleeping Beauty transposase, were numerically expanded on artificial antigen presenting cells (aAPC) derived from K562. The aAPC were genetically modified to present the target antigen CD19 along with no co-stimulation, or co-stimulation via CD86, CD137L, or both molecules. The addition of co-stimulation to the culture impacted the expression of CAR and the phenotype of the CAR+ T cells. The co-expression of a second transgene, inducible Caspase 9 (iC9) - a suicide gene, with CAR was also affected by the choice of aAPC. Furthermore, the anti-tumor activity of the CAR+ T cells numerically expanded on aAPC with or without co-stimulation was tested by adoptive transfer into mice containing CD19+ tumor. These data highlight that the use of co-stimulation in the ex vivo culture could potentially impact the therapeutic potential of CAR+ T cells.