肿瘤微环境
巨噬细胞
癌症研究
CCR2型
巨噬细胞激活因子
免疫系统
四氯化碳
血管生成
医学
表型
免疫学
生物
趋化因子
肿瘤相关巨噬细胞
淋巴因子
体外
趋化因子受体
基因
生物化学
作者
Rikke Kongsgaard Rasmussen,Anders Etzerodt
出处
期刊:Advances in pharmacology
日期:2021-01-01
卷期号:: 185-211
被引量:9
标识
DOI:10.1016/bs.apha.2021.03.002
摘要
Tumor-associated macrophages are among the most abundant non-cancerous cells in the tumor microenvironment and in many cancers macrophage infiltration into the tumor is associated with poor prognosis. Macrophages contribute to tumor development by promoting angiogenesis and immune suppression, and display remarkable phenotypic heterogeneity in the tumor microenvironment. Therapeutic strategies targeting macrophages that currently are in clinical development are mainly focused on a general depletion of tumor-associated macrophages, either by targeting the CSF-1/CSF-1R axis or by inhibiting macrophage recruitment by blocking CCR2/CCL2 signaling. Despite good pre-clinical response rates the treatment strategies focusing on general macrophage targeting have only shown limited clinical success and new approaches that target specific subsets of tumo-associated macrophages are emerging. This chapter will briefly present the functions and heterogeneity of tumor-associated macrophages and provide an overview of the current state of clinical development for pan-targeting strategies as well as discuss new strategies for targeting specific macrophage subsets for future anti-tumor immunotherapies.
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