Ontology highlight
ABSTRACT: Objective
The clinical studies of acute myeloid leukaemia (AML) revealed that antigen escaping variants cause cancer recurrence even after treatment with chimeric antigen receptor (CAR)-T cells that target a single tumour antigen. Due to the heterogeneous expression of antigens on leukaemia blasts, we hypothesized that a novel bispecific CAR, directed to the folate receptor beta (FRβ)-binding single-chain variable fragment (scFv) and an IL3α-binding receptor (CD123) that has more expression in AML blasts, can decrease CAR-T cell exhaustion and increase the efficacy of CAR-T cells to prevent antigen escaping and consequent recurrence of AML.Materials and methods
In this experimental study, the survival, proliferation, and cytolysis of CAR-T cells remains suboptimal even with
SUBMITTER: Ghamari A
PROVIDER: S-EPMC8665988 | biostudies-literature | 2021 Nov
REPOSITORIES: biostudies-literature