肿瘤微环境
免疫系统
巨噬细胞
巨噬细胞极化
嵌合抗原受体
免疫学
微泡
先天免疫系统
癌症免疫疗法
生物
免疫疗法
抗原呈递
外体
免疫
细胞因子
癌症研究
CCL18型
医学
抗原
炎症
获得性免疫系统
免疫监视
巨噬细胞激活因子
癌症
转化研究
信号转导
电池类型
分泌物
药物开发
T细胞
机制(生物学)
小RNA
作者
ZhiMei Liu,Yan Li,Jingchao Cao,Yefeng Qiu,Kun Yu,Shoulong Deng
出处
期刊:MedComm
[Wiley]
日期:2025-12-19
卷期号:7 (1): e70547-e70547
摘要
ABSTRACT Macrophages are innate immune cells that extensively infiltrate and play a key role in the tumor microenvironment (TME). Tumor cell–secreted factors recruit monocytes into the TME, where they differentiate into tumor‐associated macrophages (TAMs), which can polarize into distinct phenotypes: M1 and M2. M1 TAMs promote antitumor immunity through cytokine secretion and antigen presentation, whereas M2 TAMs support tumor progression by facilitating angiogenesis, invasion, and immune escape. Despite these dual roles, the specific mechanisms governing macrophage plasticity and polarization remain insufficiently understood. This review comprehensively summarizes the origin, polarization, and functional diversity of macrophages in the TME, with emphasis on pathways that regulate TAM‐mediated immune responses. Furthermore, this article examines current TAM‐targeted therapeutic strategies, including recruitment inhibition, phenotypic reprogramming, and the development of chimeric antigen receptor macrophages (CAR‐Ms), as well as macrophage‐based drug delivery and exosome therapy. By integrating recent advances in cell engineering and immunometabolism, this review highlights the translational potential of TAM‐targeted therapies and their value in reshaping the immunosuppressive TME to enhance cancer immunotherapy.
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