IL-10 in glioma

被引:47
|
作者
Widodo, Samuel S. [1 ]
Dinevska, Marija [1 ]
Furst, Liam M. [2 ]
Stylli, Stanley S. [1 ,3 ]
Mantamadiotis, Theo [1 ,2 ,4 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Surg, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic, Australia
[3] Royal Melbourne Hosp, Dept Neurosurg, Parkville, Vic, Australia
[4] Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
基金
英国医学研究理事会;
关键词
REGULATORY T-CELLS; TUMOR-INFILTRATING LYMPHOCYTES; TRANSCRIPTION FACTOR; GENE-EXPRESSION; C-MAF; MATRIX METALLOPROTEINASES; INITIATING CELLS; EFFECTOR-CELLS; BRAIN-TUMORS; C/EBP-BETA;
D O I
10.1038/s41416-021-01515-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis for patients with glioblastoma (GBM), the most common and malignant type of primary brain tumour, is very poor, despite current standard treatments such as surgery, radiotherapy and chemotherapy. Moreover, the immunosuppressive tumour microenvironment hinders the development of effective immunotherapies for GBM. Cytokines such as interleukin-10 (IL-10) play a major role in modulating the activity of infiltrating immune cells and tumour cells in GBM, predominantly conferring an immunosuppressive action; however, in some circumstances, IL-10 can have an immunostimulatory effect. Elucidating the function of IL-10 in GBM is necessary to better strategise and improve the efficacy of immunotherapy. This review discusses the immunostimulatory and immunosuppressive roles of IL-10 in the GBM tumour microenvironment while considering IL-10-targeted treatment strategies. The molecular mechanisms that underlie the expression of IL-10 in various cell types are also outlined, and how this resulting information might provide an avenue for the improvement of immunotherapy in GBM is explored.
引用
收藏
页码:1466 / 1476
页数:11
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