Blood Neoplasia. 2024 Nov 29;2(1):100060. doi: 10.1016/j.bneo.2024.100060. eCollection 2025 Feb.
ABSTRACT
Loss of p53 function predicts a dismal outcome in relapsed B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Chimeric antigen receptor T-cell (CAR T) therapy was recently approved to salvage relapsed/refractory BCP-ALL. We observed a significantly worse overall survival after CD19-targeting CAR T therapy in children with TP53-mutated (TP53 Mut) compared with TP53-wild-type (TP53 WT) BCP-ALL. To investigate the effect of p53 loss on CAR T therapy response, we modeled TP53 mutations in 2 BCP-ALL cell lines and observed resistance to CAR T upon p53 loss. Moreover, expression analysis in cell lines and xenografts demonstrated that loss of p53 abrogates the expression of the death receptors Fas and death receptor 5 (DR5), both implicated in CAR T cytotoxicity. Conversely, ectopic expression of Fas improved CAR T cytotoxicity. Furthermore, p53 stabilization induced expression of both Fas and DR5, accompanied by increased CAR T-mediated killing. Although these findings provide mechanistic insight into why CAR T therapy fails against TP53 Mut BCP-ALL, they may also provide opportunities to enhance the efficacy of CAR T treatment both in patients with TP53 Mut and TP53 WT BCP-ALL. Furthermore, these data underscore the need for alternative curative therapies for this very high-risk patient group.
PMID:40454411 | PMC:PMC12082145 | DOI:10.1016/j.bneo.2024.100060
