The dilemmas and possible solutions for CAR-T cell therapy application in solid tumors
Chimeric antigen receptor T (CAR-T) cell therapy, as an adoptive immunotherapy, is playing an increasingly important role in the treatment of malignant tumors. CAR-T cells are referred to as "living drugs" as they not only target tumor cells directly, but also induce long-term immune memor...
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Veröffentlicht in: | Cancer letters 2024-06, Vol.591, p.216871-216871, Article 216871 |
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Sprache: | eng |
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Zusammenfassung: | Chimeric antigen receptor T (CAR-T) cell therapy, as an adoptive immunotherapy, is playing an increasingly important role in the treatment of malignant tumors. CAR-T cells are referred to as "living drugs" as they not only target tumor cells directly, but also induce long-term immune memory that has the potential to provide long-lasting protection. CD19.CAR-T cells have achieved complete response rates of over 90 % for acute lymphoblastic leukemia and over 60 % for non-Hodgkin's lymphoma. However, the response rate of CAR-T cells in the treatment of solid tumors remains extremely low and the side effects potentially severe. In this review, we discuss the limitations that the solid tumor microenvironment poses for CAR-T application and the solutions that are being developed to address these limitations, in the hope that in the near future, CAR-T cell therapy for solid tumors can attain the same success rates as are now being seen clinically for hematological malignancies.
•The barriers of CAR-T in the treatment of solid tumors were discussed in detail.•The structure of CAR was analyzed to enhance the effect and reduce side effect.•Combined therapies were described in order to accelerate the clinical transformation of CAR-T for solid tumors. |
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ISSN: | 0304-3835 1872-7980 |
DOI: | 10.1016/j.canlet.2024.216871 |