Impact and potential value of immunosenescence on solid gastrointestinal tumors

被引:1
作者
Zhang, Tianshuai [1 ]
Wen, Rongbo [1 ]
Fan, Hao [1 ]
Yu, Yue [1 ]
Jia, Hang [1 ]
Peng, Zhiying [1 ]
Zhou, Leqi [1 ]
Yu, Guanyu [1 ]
Zhang, Wei [1 ]
机构
[1] Naval Med Univ, Changhai Hosp, Dept Colorectal Surg, Shanghai, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
基金
中国国家自然科学基金;
关键词
gastrointestinal tumors; colorectal cancer; immunosenescence; tumor microenvironment; immunotherapy; T-CELLS; B-CELLS; SUPPRESSOR-CELLS; SENESCENT CELLS; DENDRITIC CELL; COLON-CANCER; IMMUNITY; RECEPTOR; MICROENVIRONMENT; REGULATOR;
D O I
10.3389/fimmu.2024.1375730
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Solid gastrointestinal tumors often respond poorly to immunotherapy for the complex tumor microenvironment (TME), which is exacerbated by immune system alterations. Immunosenescence is the process of increased diversification of immune genes due to aging and other factors, leading to a decrease in the recognition function of the immune system. This process involves immune organs, immune cells, and the senescence-associated secretory phenotype (SASP). The most fundamental change is DNA damage, resulting in TME remodeling. The main manifestations are worsening inflammation, increased immunosuppressive SASP production, decreased immune cell antitumor activity, and the accumulation of tumor-associated fibroblasts and myeloid-derived suppressor cells, making antitumor therapy less effective. Senotherapy strategies to remove senescent cells and block key senescence processes can have synergistic effects with other treatments. This review focuses on immunoenescence and its impact on the solid TME. We characterize the immunosenescent TME and discuss future directions for antitumor therapies targeting senescence.
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页数:11
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