免疫疗法
肿瘤微环境
癌症研究
癌症免疫疗法
癌症
巨噬细胞极化
血管生成
免疫系统
巨噬细胞激活因子
先天免疫系统
人口
医学
巨噬细胞
肿瘤相关巨噬细胞
肿瘤细胞
生物
免疫学
淋巴因子
体外
内科学
环境卫生
生物化学
作者
Yongheng Shu,Ping Cheng
标识
DOI:10.1016/j.bbcan.2020.188434
摘要
Macrophages are important effector cells of the innate immune system and are also major components of the tumor microenvironment (TME). Macrophages that are abundant in the TME are called tumor-associated macrophages (TAMs). As TAMs promote strong tumor angiogenesis and support tumor cell survival, they are closely related to tumor growth. Several studies have demonstrated that reducing the density or effects of TAMs can inhibit the growth of tumors, making them targets for cancer immunotherapy, which has become a research hot spot. Several clinical and preclinical trials have studied drugs that inhibit the effects of and reduce the population of phagocytes that target TAMs achieve cancer immunotherapy. In this paper, we summarize the various methods of targeting TAMs for tumor immunotherapy, focusing on TAM mechanisms, sources, and polarization.
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