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CAR-T in cancer therapeutics and updates

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摘要 Chimeric antigen receptor (CAR) T-cell therapy has emerged as a groundbreaking approach in cancer treatment, utilizing the immune system’s capabilities to combat malignancies. This innovative therapy involves extracting T-cells from a patient’s blood, genetically modifying them to target specific cancer cells, and reinfusing them back into the patient’s body. The genetically modified T-cells then seek out and eliminate cancer cells, offering a promising therapeutic strategy. Since its initial approval in 2017, CAR-T therapy has witnessed remarkable ad- vancements and updates. Notably, CAR-T therapy, which was initially developed for hematological malignancies, has expanded its scope to target solid tumors. Currently, clinical trials are underway to explore the efficacy of CAR-T therapy in treating various solid tumors, such as lung cancer, breast cancer, and ovarian cancer. These trials hold great potential to revolutionize cancer treatment and provide new hope to patients with challenging-to-treat solid tumors. In this mini-review, we present an overview of CAR-T therapy’s mechanisms, emphasizing its role in targeting cancer cells and the potential therapeutic benefits. Additionally, we discuss the recent progress and updates in CAR-T therapy, particularly its application in treating solid tumors, and highlight the ongoing clinical trials aimed at broadening its therapeutic horizon. The evolving landscape of CAR-T therapy signifies a promising direction in cancer therapeutics, with the potential to revolutionize the treatment of both hematological and solid tumor malignancies.
作者 Shigui Zhu
出处 《Journal of the National Cancer Center》 2024年第3期189-194,共6页 癌症科学进展(英文)
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  • 1Abken, H. (2015). Adoptive therapy with CAR redirected T cells: the challenges in targeting solid tumors. Immunotherapy 7, 535-544.
  • 2Acres, B., Lacoste G., and Limacher J.M. (2015). Targeted immunotherapy designed to treat MUCl-expressing solid tumour. Curr Top Microbiol Immunol doi: 10.1007/82_2015_429.
  • 3Acres, B., and Limacher, J.M. (2005). MUC1 as a target antigen for cancer immunotherapy. Expert Rev Vaccines 4, 493-502.
  • 4Barnd, D.L., Lan, M.S., Metzgar, R.S., and Finn, O.J. (1989). Specific, major histocompatibility complex-unrestricted recognition of tu- mor-associated mucins by human cytotoxic T cells. Proc Natl Acad Sci USA 86, 7159-7163.
  • 5Barrett, D.M., Teachey, D.T., and Grupp S.A. (2014). Toxicity manage- ment for patients receiving novel T-cell engaging therapies. Curr Opin Pediatr 26, 43-49.
  • 6Beatson, R., Maurstad G., Picco G., Arulappu A., Coleman J., Wandell, H. H., Clausen, H., Mandel, U., Taylor-Papadimitriou, J., Sletmoen, M., and Burchell J.M. (2015). The breast cancer-associated glycoforms of MUC1, MUCI-Tn and sialyl-Tn, are expressed in COSMC wild-type cells and bind the C-type lectin MGL. PLoS One 10, e0125994.
  • 7Beatson, R.E., Taylor-Papadimitriou, J., and Burchell, J.M. (2010). MUC 1 immunotherapy. Immunotherapy 2, 305-327.
  • 8Blixt, O., Bueti, D., Burford, B., Allen, D., Julien, S., Hollingsworth, M., Gammerman, A., Fentiman, I., Taylor-Papadimitriou, J., and Burchell J. M. (2011). Autoantibodies to aberrantly glycosylated MUC 1 in early stage breast cancer are associated with a better prognosis. Breast Can- cer Res 13, R25.
  • 9Burchell, J., and Taylor-Papadimitriou, J. (1993). Effect of modification of carbohydrate side chains on the reactivity of antibodies with core-protein epitopes of the MUC1 gene product. Epithelial Cell Biol 2, 155-162.
  • 10Chinnasamy, D., Yu, Z., Kerkar, S.P., Zhang, L., Morgan, R.A., Restifo, N.P., and Rosenberg, S.A. (2012). Local delivery of interleukin-12 us- ing T cells targeting VEGF receptor-2 eradicates multiple vascularized tumors in mice. Clin Cancer Res 18, 1672-1683.

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