嵌合抗原受体
免疫疗法
巨噬细胞
免疫系统
肿瘤微环境
癌症免疫疗法
癌症研究
抗原
巨噬细胞激活因子
先天免疫系统
受体
免疫学
生物
医学
体外
淋巴因子
生物化学
作者
Jing Hu,Qian Yang,Zhongyu Yue,boting liao,Huijuan Cheng,Wenqi Li,Honghua Zhang,Shuling Wang,Qingchang Tian
出处
期刊:Cytotherapy
[Elsevier]
日期:2022-08-23
卷期号:25 (3): 235-244
被引量:2
标识
DOI:10.1016/j.jcyt.2022.07.001
摘要
Macrophages are versatile antigen-presenting cells. Recent studies suggest that engineered modifications of macrophages may confer better tumor therapy. Genetic engineering of macrophages with specific chimeric antigen receptors offers new possibilities for treatment of solid tumors and has received significant attention. In vitro gene editing of macrophages and infusion into the body can inhibit the immunosuppressive effect of the tumor microenvironment in solid tumors. This strategy is flexible and can be applied to all stages of cancer treatment. In contrast, nongenetic engineering tools are used to block relevant signaling pathways in immunosuppressive responses. In addition, macrophages can be loaded with drugs and engineered into cellular drug delivery systems. Here, we analyze the effect of the chimeric antigen receptor platform on macrophages and other existing engineering modifications of macrophages, highlighting their status, challenges and future perspectives. Indeed, our analyses show that new approaches in the treatment of solid tumors will likely exploit macrophages, an innate immune cell.
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