肿瘤微环境
胰腺癌
免疫系统
细胞毒性T细胞
癌症研究
巨噬细胞
体外
癌细胞
化学
癌症
抗原
肿瘤细胞
生物
免疫学
生物化学
遗传学
作者
Yongjie Zhu,Ruipu Sun,Jiawei Fan,Haiyan Ma,Bin Sun
标识
DOI:10.1097/cji.0000000000000563
摘要
Summary: A highly suppressive tumor immune microenvironment and nonspecific target endow malignant tumors with CAR-T cells. CSF1R is highly expressed on pancreatic cancer tissues compares with normal tissues in GEPIA database and M2 macrophages mainly contributing to the suppressive tumor microenvironment (TME), suggesting that CSF1R is a suitable antigen. CSF1 is the natural ligand of CSF1R, so we constructed a CSF1-CAR and tested its cytotoxic effect on tumor cells and macrophages in vitro. Our results demonstrated that CSF1-CAR-T cells can lyse tumor cells dependent on CSF1R expression. Meanwhile, CSF1-CAR-T also lyse CSF1R + M2 macrophages, suggesting that CSF1-CAR-T cells play a role in eliminating tumor cells and remodeling the TME.
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