Chimeric Antigen Receptor T Cells: a Novel Therapy for Solid Tumors
Overview
Oncology
Affiliations
The chimeric antigen receptor T (CAR-T) cell therapy is a newly developed adoptive antitumor treatment. Theoretically, CAR-T cells can specifically localize and eliminate tumor cells by interacting with the tumor-associated antigens (TAAs) expressing on tumor cell surface. Current studies demonstrated that various TAAs could act as target antigens for CAR-T cells, for instance, the type III variant epidermal growth factor receptor (EGFRvIII) was considered as an ideal target for its aberrant expression on the cell surface of several tumor types. CAR-T cell therapy has achieved gratifying breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. The third generation of CAR-T demonstrates increased antitumor cytotoxicity and persistence through modification of CAR structure. In this review, we summarized the preclinical and clinical progress of CAR-T cells targeting EGFR, human epidermal growth factor receptor 2 (HER2), and mesothelin (MSLN), as well as the challenges for CAR-T cell therapy.
CAR-T cell therapy: developments, challenges and expanded applications from cancer to autoimmunity.
Kong Y, Li J, Zhao X, Wu Y, Chen L Front Immunol. 2025; 15():1519671.
PMID: 39850899 PMC: 11754230. DOI: 10.3389/fimmu.2024.1519671.
Cell and gene therapy in neuro-oncology.
Varela M, Comba A, Faisal S, Argento A, Pena Aguelo J, Candolfi M Handb Clin Neurol. 2024; 205:297-315.
PMID: 39341660 PMC: 11441620. DOI: 10.1016/B978-0-323-90120-8.00009-5.
Overcoming Antigen Escape and T-Cell Exhaustion in CAR-T Therapy for Leukemia.
Bartoszewska E, Tota M, Kisielewska M, Skowron I, Sebastianka K, Stefaniak O Cells. 2024; 13(18.
PMID: 39329777 PMC: 11430486. DOI: 10.3390/cells13181596.
Al-Ibraheem A, Abdlkadir A, Al-Adhami D, Sathekge M, Bom H, Makoseh M Front Immunol. 2024; 15:1424269.
PMID: 39286245 PMC: 11402741. DOI: 10.3389/fimmu.2024.1424269.
Xiao W, Xu L, Wang J, Yu K, Xu B, Que Y Cancer Gene Ther. 2024; 31(10):1571-1584.
PMID: 39183354 PMC: 11489081. DOI: 10.1038/s41417-024-00823-2.