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实体瘤过继细胞治疗:当前临床格局、挑战与未来方向

英文原题:Adoptive cell therapies in solid tumors: current clinical landscape, challenges, and future directions.

PubMed 2026/05/14(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

研究概要

过继性细胞疗法(ACT)已成为肿瘤免疫治疗中的一种变革性策略,在血液系统恶性肿瘤中带来持久临床获益,并在实体瘤中不断拓展治疗潜力。

中文摘要

过继细胞疗法(ACT)已成为癌症免疫治疗领域具有变革意义的策略,可为血液系统恶性肿瘤带来持久临床获益,并拓展实体瘤治疗潜力。然而,ACT向实体恶性肿瘤转化仍受到生物学、免疫学和实际操作方面挑战的限制。本叙述性综述以循证方式概述实体瘤ACT的当前临床格局,重点关注CAR-T 细胞、TIL(肿瘤浸润淋巴细胞)及T细胞受体工程化T细胞(TCR-T)疗法。我们总结近期临床试验结局,介绍肿瘤特异性抗原靶点,并考察主要实体瘤类型中决定治疗效果的关键因素。综述讨论限制实体瘤ACT疗效的核心障碍,包括抗原异质性、免疫逃逸、T细胞迁移不足、持久性有限,以及免疫抑制性肿瘤微环境中的功能耗竭。我们还批判性评估驱动治疗耐药、靶向肿瘤外毒性,以及细胞因子释放综合征和免疫效应细胞相关神经毒性综合征等免疫相关不良事件的机制。进一步考察旨在克服这些障碍的演进策略,包括多抗原靶向、装甲型和逻辑门控CAR设计、代谢和细胞因子工程、局部区域递送,以及整合异基因和基因编辑产品的新一代生产平台。此外,我们探讨生物标志物、TME分析和个体化治疗选择在优化患者分层和提高疗效方面的作用。转化研究、联合免疫治疗和精准免疫肿瘤学的进展,是推动ACT进入下一发展阶段的关键动力。通过整合机制见解和新兴临床证据,本综述概述实体瘤ACT的进展、局限和未来方向,旨在为持续研究、临床试验设计及实体恶性肿瘤中过继细胞免疫疗法的合理应用提供前瞻性框架。

展开英文摘要原文

Adoptive cell therapy (ACT) has emerged as a transformative strategy in cancer immunotherapy, offering durable clinical benefit in hematologic malignancies and expanding therapeutic potential in solid tumors. However, the translation of ACT to solid malignancies remains constrained by biological, immunological, and logistical challenges. This narrative review provides an evidence based overview of the current clinical landscape of ACT in solid tumors, with a focus on chimeric antigen receptor T cell (CAR-T), tumor-infiltrating lymphocyte (TIL), and T cell receptor-engineered T cell (TCR-T) therapies. We summarize recent clinical trial outcomes, highlight tumor-specific antigen targets, and examine key determinants of therapeutic efficacy across major solid tumor types. The review discusses central obstacles limiting ACT success in solid tumors, including antigen heterogeneity, immune evasion, inadequate T cell trafficking, limited persistence, and functional exhaustion within the immunosuppressive tumor microenvironment. Mechanisms driving treatment resistance, on-target off-tumor toxicity, and immune-related adverse events such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome are critically evaluated. We further examine evolving strategies designed to overcome these barriers, including multi-antigen targeting, armored and logic-gated CAR designs, metabolic and cytokine engineering, locoregional delivery approaches, and next-generation manufacturing platforms incorporating allogeneic and gene-edited products. In parallel, the role of biomarkers, tumor microenvironment profiling, and personalized treatment selection is explored as a means to optimize patient stratification and enhance therapeutic outcomes. Advances in translational research, combination immunotherapy, and precision immuno-oncology are positioned as key drivers of the next phase of ACT development. By integrating mechanistic insights with emerging clinical evidence, this review outlines the progress, limitations, and future directions of ACT in solid tumors. It aims to provide a forward-looking framework to guide ongoing research, clinical trial design, and the rational implementation of adoptive cellular immunotherapies in solid malignancies.

论文信息

作者
Rizkallah J、Wehbeh BED、Wassouf W、Salameh E、Joumaa A、Haddad FJ、Hamade L、Charbel N
第一作者单位
Department of Diagnostic Radiology, American University of Beirut, Beirut, Lebanon.
通讯作者单位
Division of Hematology and Oncology, Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.
文献类型
综述
期刊
Frontiers in immunology2026
原文标识
PubMed 42220535 · DOI 10.3389/fimmu.2026.1800292