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肿瘤浸润疗法:从美国食品药品监督管理局批准到下一代方法

Tumor infiltration therapy: from FDA approval to next-generation approaches.

作者信息

Shaik Rahaman, Royyala Sai Abhistika, Inapanuri Bhanu, Durgam Akshaya, Khan Huda, Unnisa Adeeb

机构信息

Department of Pharmacology, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi, 110062, India.

Department of Pharmacology, St. Pauls College of Pharmacy, Turkayamjal, Hyderabad, Telangana, 501510, India.

出版信息

Clin Exp Med. 2025 Jul 18;25(1):254. doi: 10.1007/s10238-025-01574-6.

DOI:10.1007/s10238-025-01574-6
PMID:40679708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12274268/
Abstract

Tumor-infiltrating lymphocyte (TIL) therapy represents an emerging and promising approach in the field of cancer immunotherapy, harnessing the body's own immune cells to target and eliminate cancer cells. This review provides an in-depth analysis of TIL therapy, focusing on its mechanisms, clinical applications, challenges, and future prospects. TILs, particularly CD8 + T cells, are isolated from a patient's tumor, expanded ex vivo, and reinfused to promote anti-tumor immunity. The success of TIL therapy has been demonstrated in various cancers, particularly melanoma, where it has led to durable responses and, in some cases, complete remission. However, significant challenges remain, including the heterogeneity of TIL populations, difficulties in large-scale expansion, and immune-related adverse events. We also explore current strategies aimed at overcoming these limitations, including genetic modification of TILs, combinatory approaches with checkpoint inhibitors, and optimization of tumor infiltration protocols. With ongoing research and technological advancements, TIL therapy holds substantial promise as a cornerstone of personalized cancer treatment. This review synthesizes the current landscape of TIL therapy, providing insights into its clinical efficacy, potential for broader application, and the future of cancer immunotherapy.

摘要

肿瘤浸润淋巴细胞(TIL)疗法是癌症免疫治疗领域一种新兴且有前景的方法,它利用人体自身的免疫细胞来靶向并消除癌细胞。本综述对TIL疗法进行了深入分析,重点关注其机制、临床应用、挑战及未来前景。TIL,尤其是CD8 + T细胞,从患者肿瘤中分离出来,在体外扩增,然后重新注入以促进抗肿瘤免疫。TIL疗法的成功已在多种癌症中得到证实,尤其是黑色素瘤,在黑色素瘤治疗中它已带来持久反应,在某些情况下还实现了完全缓解。然而,仍存在重大挑战,包括TIL群体的异质性、大规模扩增的困难以及免疫相关不良事件。我们还探讨了旨在克服这些限制的当前策略,包括TIL的基因改造、与检查点抑制剂的联合方法以及肿瘤浸润方案的优化。随着研究的不断进行和技术进步,TIL疗法作为个性化癌症治疗的基石具有巨大潜力。本综述综合了TIL疗法的当前情况,深入探讨了其临床疗效、更广泛应用的潜力以及癌症免疫治疗的未来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/3d23764ed47c/10238_2025_1574_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/e1d57400a4db/10238_2025_1574_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/0615ff592ccb/10238_2025_1574_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/a0c44fe4224e/10238_2025_1574_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/2f798a0813d3/10238_2025_1574_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/3d23764ed47c/10238_2025_1574_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/e1d57400a4db/10238_2025_1574_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/0615ff592ccb/10238_2025_1574_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/a0c44fe4224e/10238_2025_1574_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce3d/12274268/2f798a0813d3/10238_2025_1574_Fig4_HTML.jpg
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本文引用的文献

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COLUMBUS 5-Year Update: A Randomized, Open-Label, Phase III Trial of Encorafenib Plus Binimetinib Versus Vemurafenib or Encorafenib in Patients With V600-Mutant Melanoma.COLUMBUS 5 年更新:依维莫司或恩考芬尼联合比尼替尼对比维莫非尼用于 V600 突变型黑色素瘤患者的随机、开放标签、III 期试验。
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