骨肉瘤
肿瘤微环境
免疫系统
癌症研究
嵌合抗原受体
免疫疗法
串扰
癌变
医学
免疫学
癌症
内科学
物理
光学
作者
Shigao Cheng,Huiyuan Wang,Xuejia Kang,Hui Zhang
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2024-02-08
卷期号:16 (2): 251-251
被引量:4
标识
DOI:10.3390/pharmaceutics16020251
摘要
Immunosuppressive elements within the tumor microenvironment are the primary drivers of tumorigenesis and malignant advancement. The presence, as well as the crosstalk between myeloid-derived suppressor cells (MDSCs), osteosarcoma-associated macrophages (OS-Ms), regulatory T cells (Tregs), and endothelial cells (ECs) with osteosarcoma cells cause the poor prognosis of OS. In addition, the consequent immunosuppressive factors favor the loss of treatment potential. Nanoparticles offer a means to dynamically and locally manipulate immuno-nanoparticles, which present a promising strategy for transforming OS-TME. Additionally, chimeric antigen receptor (CAR) technology is effective in combating OS. This review summarizes the essential mechanisms of immunosuppressive cells in the OS-TME and the current immune-associated strategies. The last part highlights the limitations of existing therapies and offers insights into future research directions.
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