肿瘤微环境
抗体依赖性细胞介导的细胞毒性
癌症研究
免疫系统
肿瘤相关巨噬细胞
肿瘤进展
细胞毒性
血管生成
巨噬细胞
转移
免疫学
生物
癌症
医学
抗体
体外
单克隆抗体
生物化学
遗传学
作者
Yutong Pan,Yinda Yu,Xiaojian Wang,Ting Zhang
标识
DOI:10.3389/fimmu.2020.583084
摘要
Tumor-associated macrophages (TAMs) represent one of the main tumor-infiltrating immune cell types and are generally categorized into either of two functionally contrasting subtypes, namely classical activated M1 macrophages and alternatively activated M2 macrophages. The former typically exerts anti-tumor functions, including directly mediate cytotoxicity and antibody-dependent cell-mediated cytotoxicity (ADCC) to kill tumor cells; the latter can promote the occurrence and metastasis of tumor cells, inhibit T cell-mediated anti-tumor immune response, promote tumor angiogenesis, and lead to tumor progression. Both M1 and M2 macrophages have high degree of plasticity and thus can be converted into each other upon tumor microenvironment changes or therapeutic interventions. As the relationship between TAMs and malignant tumors becoming clearer, TAMs have become a promising target for developing new cancer treatment. In this review, we summarize the origin and types of TAMs, TAMs interaction with tumors and tumor microenvironment, and up-to-date treatment strategies targeting TAMs.
科研通智能强力驱动
Strongly Powered by AbleSci AI