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基于细胞因子的 NK 细胞工程用于癌症免疫治疗

英文原题:Cytokine-based NK cell engineering for cancer immunotherapy.

查看英文原题

Cytokine-based NK cell engineering for cancer immunotherapy.

PubMed 2026/04/10(内容时间) Crit Rev Oncol Hematol Q1 · IF 6.2(JCR 2025)

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中文摘要

自然杀伤(NK)细胞是固有免疫系统的重要效应细胞,在抗病毒防御和抗肿瘤免疫中发挥关键作用。近年来,NK细胞已成为肿瘤免疫治疗领域的主要焦点。细胞因子构成了调控NK细胞发育、存活、增殖和效应功能的基本分子基础,同时也是NK细胞工程中的关键调控工具。本综述总结了细胞因子驱动的NK细胞工程策略及其在免疫治疗中应用的最新进展。文章概述了与NK细胞生物学相关的关键细胞因子及其调控NK细胞增殖、活化、细胞毒性、细胞因子分泌以及诱导细胞因子诱导的记忆样(CIML)NK细胞的信号通路。

进一步探讨了基于细胞因子的工程策略,特别强调IL-15介导的NK细胞扩增、功能维持和持久性支持,包括细胞因子支持的培养系统、分泌型IL-15、膜结合型IL-15(mbIL-15)以及IL-15/IL-15R融合形式。未来在精确信号调控、可控表达系统和多细胞因子协同策略方面的进展可能有助于优化治疗效果,并促进NK细胞治疗从经验性扩增方法向可编程信号设计的转变。

展开英文摘要原文

Natural killer (NK) cells are critical effector cells of the innate immune system and play essential roles in antiviral defense and antitumor immunity. In recent years, they have emerged as a major focus in the field of cancer immunotherapy. Cytokines constitute the fundamental molecular basis for regulating NK cell development, survival, proliferation, and effector functions, and also serve as key modulatory tools in NK cell engineering. This review summarizes recent progress in cytokine-driven NK cell engineering strategies and their applications in immunotherapy. It outlines the key cytokines associated with NK cell biology and the signaling pathways through which they regulate NK cell proliferation, activation, cytotoxicity, cytokine secretion, and the induction of cytokine-induced memory-like (CIML) NK cells.

It further examines cytokine-based engineering strategies, with particular emphasis on IL-15-mediated support of NK cell expansion, functional maintenance, and persistence, including cytokine-supported culture systems, secreted IL-15, membrane-bound IL-15 (mbIL-15), and IL-15/IL-15R fusion formats.

Future advances in precise signal modulation, controllable expression systems, and multi-cytokine synergistic strategies may help optimize therapeutic efficacy and facilitate the transition of NK cell therapy from empirical expansion approaches toward programmable signaling design.

论文信息

作者
Tang Q、Tian Z、Bi J
第一作者单位
Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen 518055, China; Shenzhen University of Advanced Technology, Shenzhen 518107, China; State Key Laboratory of Quantitative Synthetic Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.China
通讯作者单位
Shenzhen University of Advanced Technology, Shenzhen 518107, China; State Key Laboratory of Quantitative Synthetic Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China. Electronic address: jc.bi@siat.ac.cn.China
文献类型
综述
期刊
Critical reviews in oncology/hematology2026 Jul
原文标识
PubMed 41967617 · DOI 10.1016/j.critrevonc.2026.105333