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TIL 治疗进展:拓展黑色素瘤之外的视野

英文原题:Advances in TIL therapy: Expanding the horizons beyond melanoma.

PubMed 2025/05/16(内容时间) Med Q1 · IF 13.3(JCR 2025)

研究概要

TIL(肿瘤浸润淋巴细胞)疗法代表着实体瘤治疗的突破,满足了选择有限患者的未满足需求。

中文摘要

TIL(肿瘤浸润淋巴细胞)疗法是实体瘤治疗领域的一项突破,为治疗选择有限的患者满足了未尽需求。该疗法治疗晚期黑色素瘤的疗效已确立,在非小细胞肺癌、乳腺癌、妇科癌症及头颈部癌症中也显示出早期前景。然而,与黑色素瘤相比,T细胞浸润减少、肿瘤突变负荷(TMB)较低、免疫抑制性肿瘤微环境(TME)以及TIL治疗方案相关毒性等挑战,阻碍了其在这些患者群体中的广泛应用。为应对这些挑战,新方法聚焦于筛选肿瘤反应性TIL、优化TIL扩增、将免疫检查点抑制剂与TIL疗法联合以对抗免疫抑制性微环境,以及对TIL进行基因修饰以增强持久性和功能。需开展更大规模临床试验验证这些创新并使方案标准化。随着持续进展,TIL疗法有望重塑晚期实体癌症的治疗格局。

展开英文摘要原文

Tumor-infiltrating lymphocyte (TIL) therapy represents a breakthrough in solid tumor treatment, addressing unmet needs for patients with limited options. While its efficacy is established in advanced melanoma, TIL therapy shows early promise in non-small cell lung cancer, breast cancer, gynecological cancers, and head and neck cancers. However, challenges such as reduced T cell infiltration, lower tumor mutational burden (TMB), immunosuppressive tumor microenvironments (TME), and toxicity associated with the TIL therapy regimen hinder its broader application in these patient groups, compared with melanoma. To address these challenges, new approaches focus on the selection of tumor-reactive TIL, optimization of TIL expansion, combination of immune checkpoint inhibitors with TIL therapy to counteract immunosuppressive microenvironments, and genetic modification of TIL to enhance persistence and functionality. Larger clinical trials are essential to validate these innovations and standardize protocols. With continued advancements, TIL therapy has the potential to redefine the treatment landscape for advanced solid cancers.

论文信息

作者
Wiertsema P、Tan YH、Haanen JBAG、Seijkens TTP、Jedema I
第一作者单位
Division of Molecular Oncology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.Netherlands
通讯作者单位
Division of Molecular Oncology and Immunology, The Netherlands Cancer Institute, Amsterdam, the Netherlands. Electronic address: i.jedema@nki.nl.Netherlands
文献类型
综述
期刊
Med (New York, N.Y.)2025 Aug 8
原文标识
PubMed 40381620 · DOI 10.1016/j.medj.2025.100702