Mouse Tumor Models for Advanced Cancer Immunotherapy

被引:87
作者
Chulpanova, Dania S. [1 ]
Kitaeva, Kristina, V [1 ]
Rutland, Catrin S. [2 ]
Rizvanov, Albert A. [1 ]
Solovyeva, Valeriya V. [1 ]
机构
[1] Kazan Fed Univ, Inst Fundamental Med & Biol, Kazan 420008, Russia
[2] Univ Med, Fac Med & Hlth Sci, Nottingham NG7 2HA, England
基金
俄罗斯基础研究基金会;
关键词
cancer mouse models; cancer immunotherapy; immune checkpoint inhibitors; CAR T-cell therapy; T-CELLS; ANTITUMOR-ACTIVITY; XENOGRAFT MODELS; MICE DEFICIENT; MURINE MODEL; ENGRAFTMENT; BLOCKADE; DIFFERENTIATION; HETEROGENEITY; CRISPR/CAS9;
D O I
10.3390/ijms21114118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent advances in the development of new methods of cancer immunotherapy require the production of complex cancer animal models that reliably reflect the complexity of the tumor and its microenvironment. Mice are good animals to create tumor models because they are low cost, have a short reproductive cycle, exhibit high tumor growth rates, and can be easily genetically modified. However, the obvious problem of these models is the high failure rate observed in human clinical trials after promising results obtained in mouse models. In order to increase the reliability of the results obtained in mice, the tumor model should reflect the heterogeneity of the tumor, contain components of the tumor microenvironment, in particular immune cells, to which the action of immunotherapeutic drugs are directed. This review discusses the current immunocompetent and immunocompromised mouse models of human tumors that are used to evaluate the effectiveness of immunotherapeutic agents, in particular chimeric antigen receptor (CAR) T-cells and immune checkpoint inhibitors.
引用
收藏
页码:1 / 15
页数:15
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