基于 IL-13Rα2 人源化 scFv 的 CAR-T 细胞对胶质母细胞瘤的治疗活性

Chimeric antigen receptor (CAR)-modified T cells have exhibited impressive anti-tumor effects in both B cell malignancies and some types of solid tumors.

However, single-chain variable fragment (scFv) of a murine monoclonal antibody will induce immune responses, limit CAR-T cell persistence, and thus increase the risk of relapse.

This study successfully constructed a CAR-targeting interleukin-13 receptor 2 (IL-13R 2) according to a murine antibody, and then humanized the scFv sequence to generate another CAR. T cells expressing any of these two CARs demonstrated superior tumor inhibitory effects in vitro and in two xenograft mouse models.

However, T cells transduced with humanized CAR have an increased expansion and reduced cytokines, including interleukin-6 and interferon- . The top expressed genes clustered in leukocyte-mediated cytotoxicity, and T cell migration and immunological synapse formation contributed to the anti-glioblastoma (GBM) activity of the humanized CAR.

In conclusion, we successfully generated a humanized third-generation CAR-targeting IL-13R 2 and confirmed its anti-GBM efficacy, which provide a candidate method for clinical GBM treatment.