Mathematical deconvolution of CAR T-cell proliferation and exhaustion from real-time killing assay data.
Ontology highlight
ABSTRACT: Chimeric antigen receptor (CAR) T-cell therapy has shown promise in the treatment of haematological cancers and is currently being investigated for solid tumours, including high-grade glioma brain tumours. There is a desperate need to quantitatively study the factors that contribute to the efficacy of CAR T-cell therapy in solid tumours. In this work, we use a mathematical model of predator-prey dynamics to explore the kinetics of CAR T-cell killing in glioma: the Chimeric Antigen Receptor T-cell treatment Response in GliOma (CARRGO) model. The model includes rates of cancer cell proliferation, CAR T-cell killing, proliferation, exhaustion, and persistence. We use patient-derived and engineered cancer cell lines with an in vitro real-time cell analyser to parametrize the CARRGO mode
SUBMITTER: Sahoo P
PROVIDER: S-EPMC7014796 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature
ACCESS DATA