嵌合抗原受体
肿瘤微环境
免疫系统
免疫疗法
免疫抑制
癌症研究
巨噬细胞
血管生成
渗透(HVAC)
先天免疫系统
医学
免疫学
生物
材料科学
体外
复合材料
生物化学
作者
Yizhao Chen,Zhiying Yu,Xuewen Tan,Haifeng Jiang,Xu Zhen,Yilong Fang,Dafei Han,Wenming Hong,Wei Wei,Jiajie Tu
标识
DOI:10.1016/j.biopha.2021.111605
摘要
Chimeric antigen receptor (CAR)-T cell therapy has been shown to be an effective treatment for hematological tumors, but the treatment of solid tumors still lacks effectiveness. In the tumor microenvironment, macrophages are the innate immune cells with the highest infiltration rate. Tumor-associated macrophages (TAMs) stimulate angiogenesis, increase tumor invasion, and mediate immunosuppression. Because macrophages can infiltrate solid tumor tissue and interact with almost all cellular components in the tumor microenvironment (including tumor cells, immune cells such as T-cells, NK cells, DCs, and other resident non-immune cells), researchers are trying to use macrophages modified with CAR (CAR-M) against solid tumors. This review describes recent reports of CAR-M-based tumor treatments and summarizes their shortcomings and future applications.
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