关于小胶质细胞和巨噬细胞在胶质瘤中的作用的共识声明。

IF 10.3 1区 医学 Q1 CLINICAL NEUROLOGY
Yuqi Zheng, Islam Alzoubi, Manuel B. Graeber, Atul Anand, Lara Barazzuol, Mario Dorostkar, Karl Frontzek, Anna Golebiewska, Costas G. Hadjipanayis, Tibor Hortobagyi, Azzam Ismail, Gerard H. Jansen, Bozena Kaminska, Daniel Kirschenbaum, Yoshihiro Komohara, Bjarne Winther Kristensen, Kevin S. Lee, Emilie Le Rhun, Q. Richard Lu, Kaspar Matiasek, Christian Mawrin, Alessandro Michelucci, Nicola Montemurro, Marc-André Mouthon, Quan Liu, Regina Reimann, Roman Sankowski, Alejandro Schcolnik-Cabrera, Michael Schulz, Christian M. Schürch, Marius Schwabenland, Aurélie Tchoghandjian, Indrė Valiulytė-Simaitė, Mariano S. Viapiano, Tobias Weiss, Michael Weller, Max Wintermark
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引用次数: 0

摘要

这份国际共识声明综合了关于小胶质细胞和巨噬细胞(肿瘤相关小胶质细胞/巨噬细胞或tam)在胶质瘤进展和治疗耐药性中的复杂作用的关键发现。最近的进展强调了tam的细胞、空间和时间异质性,它们的功能可塑性,以及tam与胶质瘤干细胞和神经元微环境之间复杂的相互作用,挑战了胶质瘤中tam的M1/M2分类范式和其他误解。该声明强调,胶质瘤细胞操纵tam抑制抗肿瘤功能,而小胶质细胞介导的神经元-胶质瘤细胞相互作用调节促进肿瘤进展。此外,胶质母细胞瘤来源的细胞外囊泡(EVs)重新编程小胶质细胞以支持肿瘤进展,提供了新的治疗靶点。为了推进研究和开发更有效的治疗方法,该声明主张针对特定TAM亚群或功能进行精确治疗,使用生物工程ev作为治疗方法,并改变诸如“M1/M2”和“神经炎症”等简单术语。最终,这一新的认识可以支持调节肿瘤微环境的创新策略,将免疫抑制转化为免疫刺激,改善胶质母细胞瘤和其他类型胶质瘤患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Consensus statement on microglial and macrophage functions in gliomas

This international consensus statement synthesizes key findings on the complex roles of microglia and macrophages (tumor-associated microglia/macrophages or TAMs) in glioma progression and therapeutic resistance. Recent advances have highlighted the cellular, spatial, and temporal heterogeneity of TAMs, their functional plasticity, and the intricate interactions between TAMs, glioma stem cells, and the neuronal microenvironment, challenging the M1/M2 classification paradigm for TAMs in gliomas and other misconceptions. The statement emphasizes that glioma cells manipulate TAMs to suppress anti-tumor functions, while microglia-mediated modulation of neuron-glioma cell interactions promotes tumor progression. Furthermore, glioblastoma-derived extracellular vesicles (EVs) reprogram microglia to support tumor progression, offering novel therapeutic targets. To advance research and develop more effective treatments, the statement advocates for precision therapies targeting specific TAM subsets or functions, the use of bioengineered EVs as a therapeutic approach, and a shift away from simplistic terminology like “M1/M2” and “neuroinflammation”. Ultimately, this new understanding can support innovative strategies to modulate the tumor microenvironment, turning immunosuppression into immunostimulation and improving outcomes for patients with glioblastoma and other types of gliomas.

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来源期刊
Acta Neuropathologica
Acta Neuropathologica 医学-病理学
CiteScore
23.70
自引率
3.90%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.
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