Chimeric Antigen Receptor T cells: Priming, Cytotoxicity and the immune synapse — ASN Events

Chimeric Antigen Receptor T cells: Priming, Cytotoxicity and the immune synapse (#14)

Misty Jenkins 1
  1. Walter and Eliza Hall Institute, Parkville, VICTORIA, Australia

Chimeric antigen receptor T (CAR-T) cells have shown incredible promise in the clinic but applying this therapy as a ‘living drug’ to solid tumours comes with additional challenges and will require a deeper understanding of CAR T cell biology. Our lab investigates how triggering cells via alternative receptors influences cell fate. Firstly, I will explore the functional consequences of CAR-mediated signalling using a dual-specific CAR T cell, where the same cell was triggered via TCR or CAR and discuss the implications on the immune synapse. This study provides a mechanism for how CAR T cells can de-bulk large tumor burden quickly and may contribute to further refinement of CAR design for enhancing the quality of signalling and programming of the T cell. Secondly, I will provide a rationale for exploring the role of CAR T cell priming on influencing T cell fate, including T cell proliferation and survival.

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