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]
Summary
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
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.