Nanomaterials-Involved Tumor-Associated Macrophages' Reprogramming for Antitumor Therapy

被引:9
|
作者
Li, Shu-Lan [1 ,2 ]
Hou, Hua-Ying [3 ,4 ]
Chu, Xu [1 ,2 ]
Zhu, Yu-Ying [1 ,2 ]
Zhang, Yu-Juan [3 ,4 ]
Duan, Meng-Die [3 ,4 ]
Liu, Junyi [6 ]
Liu, Yi [1 ,2 ,3 ,4 ,5 ]
机构
[1] Tiangong Univ, Sch Chem, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[2] Tiangong Univ, Sch Elect & Informat Engn, Tianjin 300387, Peoples R China
[3] Tiangong Univ, Sch Mat Sci & Engn, Tianjin 300387, Peoples R China
[4] Tiangong Univ, Sch Chem Engn & Technol, Tianjin 300387, Peoples R China
[5] Wuhan Polytech Univ, Sch Chem & Environm Engn, Wuhan 430023, Peoples R China
[6] Albany Med Coll, New York, NY 12208 USA
基金
中国国家自然科学基金;
关键词
tumor-associated macrophages; polarization; reprogramming; nanomaterials; tumor microenvironment; immunotherapy; combination therapy; antitumor; NF-KAPPA-B; CHECKPOINT-BLOCKADE; CANCER-THERAPY; PROTEIN-KINASE; NITRIC-OXIDE; IN-VIVO; POLARIZATION; CELLS; IMMUNOTHERAPY; NANOPARTICLES;
D O I
10.1021/acsnano.3c12387
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tumor-associated macrophages (TAMs) play pivotal roles in tumor development. As primary contents of tumor environment (TME), TAMs secrete inflammation-related substances to regulate tumoral occurrence and development. There are two kinds of TAMs: the tumoricidal M1-like TAMs and protumoral M2-like TAMs. Reprogramming TAMs from immunosuppressive M2 to immunocompetent M1 phenotype is considered a feasible way to improve immunotherapeutic efficiency. Notably, nanomaterials show great potential for biomedical fields due to their controllable structures and properties. There are many types of nanomaterials that exhibit great regulatory activities for TAMs' reprogramming. In this review, the recent progress of nanomaterials-involved TAMs' reprogramming is comprehensively discussed. The various nanomaterials for TAMs' reprogramming and the reprogramming strategies are summarized and introduced. Additionally, the challenges and perspectives of TAMs' reprogramming for efficient therapy are discussed, aiming to provide inspiration for TAMs' regulator design and promote the development of TAMs-mediated immunotherapy.
引用
收藏
页码:7769 / 7795
页数:27
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