Abstract

Chimeric antigen receptor T cells (CAR T cells) are engineered cells expressing a chimeric antigen receptor (CAR) against a specific tumor antigen (TA) that allows for the identification and elimination of cancer cells. The remarkable clinical effect seen with CAR T cell therapies against hematological malignancies have attracted interest in developing such therapies for solid tumors, including brain tumors. Glioblastoma (GBM) is the most common primary brain tumor in adults and is associated with poor prognosis due to its highly aggressive nature. Pediatric brain cancers are similarly aggressive and thus are a major cause of pediatric cancer-related death. CAR T cell therapy represents a promising avenue for therapy against these malignancies. Several specific TAs, such as EGFR/EGFRvIII, IL13Rα2, B7-H3, and HER2, have been targeted in preclinical studies and clinical trials. Unfortunately, CAR T cells against brain tumors have showed limited efficacy due to TA heterogeneity, difficulty trafficking from blood to tumor sites, and the immunosuppressive tumor microenvironment. Here, we review current CAR T cell approaches in treating cancers, with particular focus on brain cancers. We also describe a novel technique of focused ultrasound controlling the activation of engineered CAR T cells to achieve the safer cell therapies. Finally, we summarize the development of combinational strategies to improve the efficacy and overcome historical limitations of CAR T cell therapy.

Highlights

  • T cells engineered to express chimeric antigen receptors (CAR T cells) have shown remarkable efficacy in treatment of hematological cancer and represent a promising frontier for innovation in their application to treat solid malignancies [1]

  • CAR T therapies have been developed for chronic lymphoblastic leukemia (CLL) and acute lymphoblastic leukemia (ALL), as well as recurrent lymphoma and prostate cancer, and investigation continues for optimizations that prove clinical effectiveness in other malignancies [1]

  • This study found EGFRvIII loss or decreased expression in resected tumors of most patients treated with CAR T cell infusion [23]

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Summary

INTRODUCTION

T cells engineered to express chimeric antigen receptors (CAR T cells) have shown remarkable efficacy in treatment of hematological cancer and represent a promising frontier for innovation in their application to treat solid malignancies [1]. Chimeric antigen receptors (CARs), which are assembled by the fusion of a recognition domain, single-chain antibody and T cell stimulatory domain, can be engineered to recognize a target antigen without major histocompatibility complex (MHC) presentation [2, 3]. These CAR constructs are transfected into T cells using plasmids, mRNA, or viral vector transduction to display on the cell surface. CAR T cells can be engineered to target virtually any antigen, such as tumor-associated antigens or microbial antigens

CAR T Cells in Primary Brain Tumors
CAR T CELL THERAPY IN HEMATOLOGIC CANCER
CAR T CELL THERAPY IN SOLID TUMORS
CAR T THERAPY FOR BRAIN TUMORS
Pediatric Brain Tumor
Study phase
FOCUSED ULTRASOUND TO MEDIATE CAR T FUNCTION
STRATEGIES TO ENHANCE CAR T CELLS THERAPY
Findings
CONCLUSION

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