The IAP antagonist birinapant enhances chimeric antigen receptor T cell therapy for glioblastoma by overcoming antigen heterogeneity

Antigen heterogeneity that results in tumor antigenic escape is one of the major obstacles to successful chimeric antigen recep-tor (CAR) T cell therapies in solid tumors including glioblas-toma multiforme (GBM). To address this issue and improve the efficacy of CAR T cell therapy for GBM, we developed an approach that combines CAR T cells with inhibitor of apoptosis protein (IAP) antagonists, a new class of small mol-ecules that mediate the degradation of IAPs, to treat GBM. Here, we demonstrated that the IAP antagonist birinapant could sensitize GBM cell lines and patient-derived primary GBM organoids to apoptosis induced by CART cell-derived cy-tokines, such as tumor necrosis factor. Therefore, birinapant could enhance CAR T cell-mediated bystander death of anti-gen-negative GBM cells, thus preventing tumor antigenic escape in antigen-heterogeneous tumor models in vitro and in vivo. In addition, birinapant could promote the activation of NF -KB signaling pathways in antigen-stimulated CAR T cells, and with a birinapant-resistant tumor model we showed that birinapant had no deleterious effect on CAR T cell func-tions in vitro and in vivo. Overall, we demonstrated the poten-tial of combining the IAP antagonist birinapant with CAR T cells as a novel and feasible approach to overcoming tumor antigen heterogeneity and enhancing CAR T cell therapy for GBM.

Automated summary

The study demonstrates that using IAP antagonist birinapant can enhance the efficacy of CAR T cell therapy for glioblastoma, effectively preventing tumor antigenic escape and increasing CAR T cell-mediated bystander death of glioblastoma cells.