Humanized mouse models for immuno-oncology research

被引:211
作者
Chuprin, Jane [1 ,2 ]
Buettner, Hannah [1 ,3 ]
Seedhom, Mina O. [1 ]
Greiner, Dale L. [1 ]
Keck, James G. [4 ]
Ishikawa, Fumihiko [5 ]
Shultz, Leonard D. [6 ]
Brehm, Michael A. [1 ]
机构
[1] Univ Massachusetts, Program Mol Med, Chan Med Sch, Worcester, MA 01003 USA
[2] Univ Massachusetts, Dept Mol Cell & Canc Biol, Chan Med Sch, Worcester, MA USA
[3] Univ Massachusetts, Dept Surg, Chan Med Sch, Worcester, MA USA
[4] Jackson Lab, Sacramento, CA USA
[5] Riken Ctr Integrat Med Sci, Yokohama, Japan
[6] Jackson Lab, Bar Harbor, ME USA
基金
日本学术振兴会; 美国国家卫生研究院;
关键词
ACUTE MYELOID-LEUKEMIA; HEMATOPOIETIC STEM-CELLS; REGULATORY PROTEIN ALPHA; VERSUS-HOST-DISEASE; T-CELLS; ANTITUMOR-ACTIVITY; PROGENITOR CELLS; IN-VIVO; TUMOR-MICROENVIRONMENT; IMMUNOLOGICAL FUNCTION;
D O I
10.1038/s41571-022-00721-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy has emerged as a promising treatment paradigm for many malignancies and is transforming the drug development landscape. Although immunotherapeutic agents have demonstrated clinical efficacy, they are associated with variable clinical responses, and substantial gaps remain in our understanding of their mechanisms of action and specific biomarkers of response. Currently, the number of preclinical models that faithfully recapitulate interactions between the human immune system and tumours and enable evaluation of human-specific immunotherapies in vivo is limited. Humanized mice, a term that refers to immunodeficient mice co-engrafted with human tumours and immune components, provide several advantages for immuno-oncology research. In this Review, we discuss the benefits and challenges of the currently available humanized mice, including specific interactions between engrafted human tumours and immune components, the development and survival of human innate immune populations in these mice, and approaches to study mice engrafted with matched patient tumours and immune cells. We highlight the latest advances in the generation of humanized mouse models, with the aim of providing a guide for their application to immuno-oncology studies with potential for clinical translation.
引用
收藏
页码:192 / 206
页数:15
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