Assessment of IFNγ responsiveness in patient-derived xenografts

被引:1
|
作者
Cardenas, Jordan J. [1 ]
Robles-Oteiza, Camila [1 ]
Politi, Katerina [2 ,3 ,4 ]
机构
[1] Yale Sch Med, Dept Immunobiol, New Haven, CT USA
[2] Yale Sch Med, Dept Pathol, New Haven, CT 06510 USA
[3] Yale Sch Med, Dept Med, Sect Med Oncol, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Yale Canc Ctr, New Haven, CT 06510 USA
来源
TUMOR IMMUNOLOGY AND IMMUNOTHERAPY - CELLULAR METHODS, PT A | 2020年 / 631卷
关键词
IMMUNE CHECKPOINT INHIBITORS; ACQUIRED-RESISTANCE;
D O I
10.1016/bs.mie.2019.10.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patient-derived xenografts are a useful tool in cancer immunology, as they allow researchers to study human cancers in vivo when starting with a relatively small amount of human tumor tissue. These models make it possible to study tumor cell-intrinsic changes that occur in response to external stimuli including cytokines like interferon gamma (IFN gamma) that are important for effective anti-tumor immune responses. IFN gamma responsiveness can be measured by assessing surface expression of MHC class I on tumor cells, the molecule on which tumor antigens are presented to cytotoxic T cells in the tumor microenvironment. Low levels of MHC class I and lack of responsiveness have been associated with resistance to T-cell directed therapies like immune checkpoint inhibitors. In this chapter, we present a protocol for an assay to screen patient-derived xenografts for their responsiveness to IFN gamma. The results of this assay can be used as a starting point for uncovering cancer cell-intrinsic mechanisms of resistance to immunotherapies in patient tumors.
引用
收藏
页码:415 / 427
页数:13
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