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脑癌中微胶质细胞与T细胞之间的不同串扰:对新型治疗策略的启示

Divergent Crosstalk Between Microglia and T Cells in Brain Cancers: Implications for Novel Therapeutic Strategies.

作者信息

Yi Min-Hee, Lee Jinkyung, Moon Subin, So EunA, Bang Geonhyeok, Moon Kyung-Sub, Lee Kyung-Hwa

机构信息

Department of Microbiology and Immunology, Chonnam National University Medical School, Hwasun 58128, Jeollanam-do, Republic of Korea.

Biomedical Sciences Graduate Program (BMSGP), Chonnam National University, Hwasun 58128, Jeollanam-do, Republic of Korea.

出版信息

Biomedicines. 2025 Jan 16;13(1):216. doi: 10.3390/biomedicines13010216.

DOI:10.3390/biomedicines13010216
PMID:39857798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11763300/
Abstract

: Brain cancers represent a formidable oncological challenge characterized by their aggressive nature and resistance to conventional therapeutic interventions. The tumor microenvironment has emerged as a critical determinant of tumor progression and treatment efficacy. Within this complex ecosystem, microglia and macrophages play fundamental roles, forming intricate networks with peripheral immune cell populations, particularly T cells. The precise mechanisms underlying microglial interactions with T cells and their contributions to immunosuppression remain incompletely understood. : This review comprehensively examines the complex cellular dialogue between microglia and T cells in two prominent brain malignancies: primary glioblastoma and secondary brain metastases. : Through a comprehensive review of the current scientific literature, we explore the nuanced mechanisms through which microglial-T cell interactions modulate tumor growth and immune responses. : Our analysis seeks to unravel the cellular communication pathways that potentially underpin tumor progression, with the ultimate goal of illuminating novel therapeutic strategies for brain cancer intervention.

摘要

脑癌是一种严峻的肿瘤学挑战,其特点是具有侵袭性且对传统治疗干预具有抗性。肿瘤微环境已成为肿瘤进展和治疗效果的关键决定因素。在这个复杂的生态系统中,小胶质细胞和巨噬细胞发挥着重要作用,与外周免疫细胞群体,特别是T细胞形成复杂的网络。小胶质细胞与T细胞相互作用的精确机制及其对免疫抑制的作用仍未完全了解。 本综述全面研究了两种主要脑恶性肿瘤——原发性胶质母细胞瘤和继发性脑转移瘤中小胶质细胞与T细胞之间复杂的细胞对话。 通过对当前科学文献的全面综述,我们探索了小胶质细胞 - T细胞相互作用调节肿瘤生长和免疫反应的细微机制。 我们的分析旨在揭示可能支撑肿瘤进展的细胞通讯途径,最终目标是为脑癌干预阐明新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70aa/11763300/0bc80839f042/biomedicines-13-00216-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70aa/11763300/0bc80839f042/biomedicines-13-00216-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70aa/11763300/0bc80839f042/biomedicines-13-00216-g001.jpg

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本文引用的文献

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Targeting the HSP47-collagen axis inhibits brain metastasis by reversing M2 microglial polarization and restoring anti-tumor immunity.靶向 HSP47-胶原轴通过逆转 M2 小胶质细胞极化和恢复抗肿瘤免疫来抑制脑转移。
Cell Rep Med. 2024 May 21;5(5):101533. doi: 10.1016/j.xcrm.2024.101533. Epub 2024 May 13.
2
Microglia Suppresses Breast Cancer Brain Metastasis via a Pro-inflammatory Response.小胶质细胞通过促炎反应抑制乳腺癌脑转移。
Neurosci Bull. 2024 Jul;40(7):1034-1036. doi: 10.1007/s12264-024-01217-y. Epub 2024 May 6.
3
Blocking the MIF-CD74 axis augments radiotherapy efficacy for brain metastasis in NSCLC via synergistically promoting microglia M1 polarization.
阻断 MIF-CD74 轴通过协同促进小胶质细胞 M1 极化增强 NSCLC 脑转移的放疗疗效。
J Exp Clin Cancer Res. 2024 Apr 29;43(1):128. doi: 10.1186/s13046-024-03024-9.
4
Targeting PD-1/PD-L-1 immune checkpoint inhibition for cancer immunotherapy: success and challenges.靶向PD-1/PD-L-1免疫检查点抑制用于癌症免疫治疗:成功与挑战
Front Immunol. 2024 Apr 10;15:1383456. doi: 10.3389/fimmu.2024.1383456. eCollection 2024.
5
Oncolytic adenovirus in treating malignant ascites: A phase II trial and longitudinal single-cell study.溶瘤腺病毒治疗恶性腹水:Ⅱ期临床试验和纵向单细胞研究。
Mol Ther. 2024 Jun 5;32(6):2000-2020. doi: 10.1016/j.ymthe.2024.04.029. Epub 2024 Apr 24.
6
Microglia and macrophage metabolism: a regulator of cerebral gliomas.小胶质细胞与巨噬细胞代谢:脑胶质瘤的一种调节因子
Cell Biosci. 2024 Apr 17;14(1):49. doi: 10.1186/s13578-024-01231-7.
7
The paradoxical role of cytokines and chemokines at the tumor microenvironment: a comprehensive review.细胞因子和趋化因子在肿瘤微环境中的矛盾作用:全面综述。
Eur J Med Res. 2024 Feb 15;29(1):124. doi: 10.1186/s40001-024-01711-z.
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