摘要：SummaryChimeric antigen receptors (CARs) are engineered receptors that mediate T cell activation. CARs are comprised of activating and co-stimulatory intracellular signaling domains derived from endogenous T cells that initiate signaling required for T cell activation, including ERK activation through the MAPK pathway. Understanding the mechanisms by which co-stimulatory domains influence signaling can help guide the design of next-generation CARs. Therefore, we constructed an experimentally validated computational model of anti-CD19 CARs in T cells bearing the CD3ζ domain alone or in combination with CD28. We performed a systematic analysis to explore the different mechanisms of CD28 co-stimulation on the ERK response time. Comparing these model simulations with experimental data indicates that CD28 primarily influences ERK activation by enhancing the phosphorylation kinetics of CD3ζ. Overall, we present a mechanistic mathematical modeling framework that can be used to gain insights into the mechanism of CAR T cell activation and produce new testable hypotheses.Graphical AbstractDisplay OmittedHighlights•We construct a mathematical model to explore CAR-mediated MAPK signaling•Model predicts how intracellular CAR domains affect ERK response time•CD28 influences ERK activation by enhancing the phosphorylation kinetics of CD3ζ•Removing ITAMs from CD3ζ speeds up ERK response and reduces negative feedbackImmunology; Immunology Theories; Computational Bioinformatics
