Promoter usage regulating the surface density of CAR molecules may modulate the kinetics of CAR-T cells in vivo.
Ontology highlight
ABSTRACT: Although chimeric antigen receptor T (CAR-T) cell therapy achieves high remission rates, challenges (e.g., toxicity management and relapse prevention) remain. The major risks are cytokine release syndrome and related neurological toxicity. The influence of the CAR surface density on the efficacy/safety of CAR-T cell therapy and the factors determining CAR density were not elucidated comprehensively. Here, we discovered that the use of the MND promoter increased the transduction rate and reduced the CAR surface density. Additionally, MND-driven CAR-T cells had prolonged antileukemia activity in a mouse model. In an initial dual-armed anti-CD19 CAR-T cell pilot study (ClinicalTrials.gov: NCT03840317), eight and six subjects were infused with MND and EF1α promoter-driven autologous CAR-T cell
SUBMITTER: Ho JY
PROVIDER: S-EPMC8027690 | biostudies-literature | 2021 Jun
REPOSITORIES: biostudies-literature
ACCESS DATA