Background
T cells can be genetically engineered to target a specific cell surface marker that is present on cancer cells, and this form of therapy, termed chimeric antigen receptor (CAR) T cells, has been highly successful in the treatment of pediatric acute lymphoblastic leukemia (ALL). We propose to adapt CAR T cell therapy to meet the unmet needs of children with acute myeloid leukemia (AML), a disease with suboptimal clinical outcomes.