嵌合抗原受体
肿瘤微环境
癌症研究
实体瘤
缺氧(环境)
肿瘤细胞
体外
重编程
化学
细胞
T细胞
癌症
生物
医学
免疫学
免疫系统
内科学
生物化学
氧气
有机化学
作者
Jeong Min Oh,K. Robert Shen
出处
期刊:Methods in molecular biology
日期:2023-12-09
卷期号:: 119-134
被引量:1
标识
DOI:10.1007/978-1-0716-3593-3_10
摘要
Solid tumors contain abnormal physical and biochemical barriers that hinder chimeric antigen receptor (CAR) T cell therapies. However, there is a lack of understanding on how the solid tumor microenvironment (e.g. hypoxia) modulates CAR-T cell function. Hypoxia is a common feature of many advanced solid tumors that contributes to reprogramming of cancer and T cell metabolism as well as their phenotypes and interactions. To gain insights into the activities of CAR-T cells in solid tumors and to assess the effectiveness of new combination treatments involving CAR-T cells, in vitro models that faithfully reflect CAR-T cell–solid tumor interactions under physiologically relevant tumor microenvironment is needed. Here we demonstrate how to establish a hypoxic 3-dimensional (3-D) tumor model using a cleanroom-free, micromilling-based microdevice and assess the efficacy of the combination treatment with CAR-T cells and PD-1/PD-L1 inhibition.
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