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通过巨噬细胞调控增强自然杀伤细胞的抗肿瘤活性。

Enhancing natural killer cell anti-tumour activity through macrophage manipulation.

作者信息

Palmer Natasha, Khakoo Salim, Sanchez-Elsner Tilman, Vallejo Andres F

机构信息

School of Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, Southampton, United Kingdom.

出版信息

Front Immunol. 2025 Aug 29;16:1656925. doi: 10.3389/fimmu.2025.1656925. eCollection 2025.

DOI:10.3389/fimmu.2025.1656925
PMID:40948757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12426019/
Abstract

The tumour microenvironment (TME) is a complex and dynamic environment containing diverse cellular, stromal and soluble factors, that collectively influence cancer progression, immune evasion and therapeutic resistance. Among the immune components of the TME, macrophages and natural killer (NK) cells are key players, whose interactions, particularly their crosstalk, critically shape anti-tumour immunity. The macrophage-NK cell interplay can either promote or suppress immune responses depending on the context, representing both a challenge and a therapeutic opportunity. NK cells are key effectors capable of recognising and eliminating malignant cells without prior sensitisation, whereas macrophages exhibit remarkable plasticity, functioning as either promoters or suppressors of tumour immunity depending on their activation state. This review focuses on current strategies to harness macrophages in cancer therapy, including phenotype repolarisation, selective depletion, and disruption or enhancement of the macrophage-NK cell crosstalk to enhance NK cell-mediated tumour surveillance. Finally, we highlight emerging technologies, such as single-cell RNA sequencing, spatial transcriptomics, and proteomics, as powerful tools to elucidate the dynamic interplay between macrophages and NK cells and inform the next generation of immunotherapeutic interventions.

摘要

肿瘤微环境(TME)是一个复杂且动态的环境,包含多种细胞、基质和可溶性因子,它们共同影响癌症进展、免疫逃逸和治疗抗性。在TME的免疫成分中,巨噬细胞和自然杀伤(NK)细胞是关键参与者,它们之间的相互作用,尤其是它们的串扰,对抗肿瘤免疫起着至关重要的塑造作用。巨噬细胞与NK细胞的相互作用根据具体情况既可以促进也可以抑制免疫反应,这既代表了一种挑战,也代表了一个治疗机会。NK细胞是关键效应细胞,能够在无需预先致敏的情况下识别并消除恶性细胞,而巨噬细胞则表现出显著的可塑性,根据其激活状态发挥肿瘤免疫促进者或抑制者的作用。本综述聚焦于当前在癌症治疗中利用巨噬细胞的策略,包括表型重极化、选择性清除,以及破坏或增强巨噬细胞与NK细胞的串扰以增强NK细胞介导的肿瘤监测。最后,我们强调了新兴技术,如单细胞RNA测序、空间转录组学和蛋白质组学,作为阐明巨噬细胞与NK细胞之间动态相互作用并为下一代免疫治疗干预提供信息的强大工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/58a93a62b672/fimmu-16-1656925-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/ffc314248b7f/fimmu-16-1656925-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/8a0a7bb0b66b/fimmu-16-1656925-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/58a93a62b672/fimmu-16-1656925-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/ffc314248b7f/fimmu-16-1656925-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/c26bc721b772/fimmu-16-1656925-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/1b2a3890ef29/fimmu-16-1656925-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8486/12426019/58a93a62b672/fimmu-16-1656925-g005.jpg

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本文引用的文献

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PSGL-1 is a phagocytosis checkpoint that enables tumor escape from macrophage clearance.P选择素糖蛋白配体-1(PSGL-1)是一种吞噬作用检查点,可使肿瘤逃避巨噬细胞的清除。
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The inhibitory receptor LAG3 affects NK cell IFN-γ production through glycolysis and the PSAT1/STAT1/IFNG pathway.抑制性受体LAG3通过糖酵解和PSAT1/STAT1/IFNG途径影响自然杀伤细胞的γ干扰素产生。
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Targeting MARCO in combination with anti-CTLA-4 leads to enhanced melanoma regression and immune cell infiltration via macrophage reprogramming.
联合靶向MARCO与抗CTLA-4可通过巨噬细胞重编程增强黑色素瘤消退和免疫细胞浸润。
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Interactions of NK Cells and Macrophages: From Infections to Cancer Therapeutics.自然杀伤细胞与巨噬细胞的相互作用:从感染到癌症治疗
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Targeting CD206+ macrophages disrupts the establishment of a key antitumor immune axis.靶向 CD206+ 巨噬细胞会破坏关键抗肿瘤免疫轴的建立。
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Dichotomous outcomes of TNFR1 and TNFR2 signaling in NK cell-mediated immune responses during inflammation.在炎症期间 NK 细胞介导的免疫反应中,TNFR1 和 TNFR2 信号的二分结果。
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In-Depth Proteomic Analysis Reveals Phenotypic Diversity of Macrophages in Liver Fibrosis.深入的蛋白质组学分析揭示了肝纤维化中巨噬细胞的表型多样性。
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Unveiling the impact of TREM-2 Macrophages in metabolic disorders.揭示 TREM-2 巨噬细胞在代谢紊乱中的作用。
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Single-cell RNA sequencing reveals the change in cytotoxic NK/T cells, epithelial cells and myeloid cells of the tumor microenvironment of high-grade serous ovarian carcinoma.单细胞RNA测序揭示了高级别浆液性卵巢癌肿瘤微环境中细胞毒性NK/T细胞、上皮细胞和髓样细胞的变化。
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Single-cell sequencing combined with spatial transcriptomics reveals that the IRF7 gene in M1 macrophages inhibits the occurrence of pancreatic cancer by regulating lipid metabolism-related mechanisms.单细胞测序联合空间转录组学揭示 M1 巨噬细胞中的 IRF7 基因通过调控脂质代谢相关机制抑制胰腺癌的发生。
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