小胶质细胞
肿瘤微环境
胶质母细胞瘤
免疫抑制
免疫系统
胶质瘤
癌症研究
生物
中枢神经系统
免疫学
人口
神经科学
医学
炎症
环境卫生
作者
Fatima Khan,Lizhi Pang,Madeline Dunterman,Maciej S. Lesniak,Amy B. Heimberger,Peiwen Chen
摘要
Glioblastoma (GBM) is the most aggressive tumor in the central nervous system and contains a highly immunosuppressive tumor microenvironment (TME). Tumor-associated macrophages and microglia (TAMs) are a dominant population of immune cells in the GBM TME that contribute to most GBM hallmarks, including immunosuppression. The understanding of TAMs in GBM has been limited by the lack of powerful tools to characterize them. However, recent progress on single-cell technologies offers an opportunity to precisely characterize TAMs at the single-cell level and identify new TAM subpopulations with specific tumor-modulatory functions in GBM. In this Review, we discuss TAM heterogeneity and plasticity in the TME and summarize current TAM-targeted therapeutic potential in GBM. We anticipate that the use of single-cell technologies followed by functional studies will accelerate the development of novel and effective TAM-targeted therapeutics for GBM patients.
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