装甲嵌合抗原受体(CAR) T细胞作为癌症治疗的微药物。

C. Carcopino , E. Erdogan , M. Henrich , S. Kobold
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引用次数: 0

摘要

嵌合抗原受体(CAR)- t细胞疗法已成为对抗癌症的有力武器。然而,其疗效经常受到肿瘤渗透有限、抗原逃逸和肿瘤微环境内免疫抑制等挑战的阻碍。这篇综述探讨了装甲CAR-T细胞或“微药物”在克服这些障碍和提高过继t细胞(ATC)治疗效果方面的潜力。我们深入研究了这些先进疗法背后的工程策略,以及它们提高car - t细胞疗效的机制。此外,我们还讨论了该领域的最新进展和研究成果,全面了解了装甲CAR-T细胞在癌症治疗中的作用。最后,本综述强调了将微药整合到ATC治疗中的前景,为更有效和更有针对性的癌症治疗铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Armoring chimeric antigen receptor (CAR) T cells as micropharmacies for cancer therapy
Chimeric antigen receptor (CAR)-T-cell therapy has emerged as a powerful weapon in the fight against cancer. However, its efficacy is often hindered by challenges such as limited tumor penetration, antigen escape, and immune suppression within the tumor microenvironment. This review explores the potential of armored CAR-T cells, or ‘micropharmacies’, in overcoming these obstacles and enhancing the therapeutic outcomes of adoptive T-cell (ATC) therapy. We delve into the engineering strategies behind these advanced therapies and the mechanisms through which they improve CAR-T-cell efficacy. Additionally, we discuss the latest advancements and research findings in the field, providing a comprehensive understanding of the role of armored CAR-T cells in cancer treatment. Ultimately, this review highlights the promising future of integrating micropharmacies into ATC therapy, paving the way for more effective and targeted cancer treatments.
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