CD19 CAR antigen engagement mechanisms and affinity tuning

Chimeric antigen receptor (CAR) T cell therapy relies on T cells that are guided by synthetic receptors to target and lyse cancer cells. CARs bind to cell surface antigens through an scFv (binder), the affinity of which is central to determining CAR T cell function and therapeutic success. CAR T cells targeting CD19 were the first to achieve marked clinical responses in patients with relapsed/refractory B cell malignancies and to be approved by the U.S. Food and Drug Administration (FDA). We report cryo-EM structures of CD19 antigen with the binder FMC63, which is used in four FDA-approved CAR T cell therapies (Kymriah, Yescarta, Tecartus, and Breyanzi), and the binder SJ25C1, which has also been used extensively in multiple clinical trials. We used these structures for mo-lecular dynamics simulations, which guided creation of lower-or higher-affinity binders, and ultimately pro-duced CAR T cells endowed with distinct tumor recognition sensitivities. The CAR T cells exhibited different antigen density requirements to trigger cytolysis and differed in their propensity to prompt trogocytosis upon contacting tumor cells. Our work shows how structural information can be applied to tune CAR T cell per-formance to specific target antigen densities.

Automated summary

CAR T cell therapy utilizes synthetic receptors to guide T cells in targeting and destroying cancer cells. By studying cryo-EM structures and conducting molecular dynamics simulations, researchers were able to create CAR T cells with different tumor recognition sensitivities and understand their requirements for cytolysis and trogocytosis.