嵌合抗原受体
免疫疗法
癌症免疫疗法
癌症研究
肿瘤微环境
渗透(HVAC)
T细胞
CD8型
细胞毒性T细胞
抗原
免疫系统
生物
免疫学
肿瘤细胞
体外
材料科学
复合材料
生物化学
作者
Duo Zhang,Elisavet Krimitza,Katherine Han,Ruiying Su,David J. Xu,Jaiden R. Xu,Yanqing Gong,Yi Fan
出处
期刊:STAR protocols
[Elsevier BV]
日期:2024-02-16
卷期号:5 (1): 102898-102898
被引量:5
标识
DOI:10.1016/j.xpro.2024.102898
摘要
The efficacy of chimeric antigen receptor (CAR) T cell immunotherapy is limited by insufficient infiltration and activation of T cells due to the immunosuppressive tumor microenvironment. Preclinical studies with optimized mouse CAR T cells in immunocompetent mouse cancer models will help define the mechanisms underlying immunotherapy resistance. Here, we present a protocol for preparing mouse T cells and generating CAR T cells. We then detail procedures for testing their therapeutic efficacy and tracking them in a syngeneic mouse glioma model. For complete details on the use and execution of this protocol, please refer to Zhang et al.1
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