Cargando…

Quantitative evaluation of the immunodeficiency of a mouse strain by tumor engraftments

BACKGROUND: The mouse is an organism that is widely used as a mammalian model for studying human physiology or disease, and the development of immunodeficient mice has provided a valuable tool for basic and applied human disease research. Following the development of large-scale mouse knockout progr...

Descripción completa

Detalles Bibliográficos
Autores principales: Ye, Wei, Jiang, Zhiwu, Li, Guan-Xiong, Xiao, Yiren, Lin, Simiao, Lai, Yunxin, Wang, Suna, Li, Baiheng, Jia, Bei, Li, Yin, Huang, Zhi-liang, Li, Jin, Feng, Fenglan, Li, Shuhua, Yao, Huihui, Liu, Zixia, Cao, Su, Xu, Lin, Li, Yangqiu, Wu, Donghai, Zeng, Lingwen, Zhong, Mei, Liu, Pentao, Wen, Zhe-sheng, Xu, Bing, Yao, Yao, Pei, Duanqing, Li, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478639/
https://www.ncbi.nlm.nih.gov/pubmed/26022250
http://dx.doi.org/10.1186/s13045-015-0156-y
Descripción
Sumario:BACKGROUND: The mouse is an organism that is widely used as a mammalian model for studying human physiology or disease, and the development of immunodeficient mice has provided a valuable tool for basic and applied human disease research. Following the development of large-scale mouse knockout programs and genome-editing tools, it has become increasingly efficient to generate genetically modified mouse strains with immunodeficiency. However, due to the lack of a standardized system for evaluating the immuno-capacity that prevents tumor progression in mice, an objective choice of the appropriate immunodeficient mouse strains to be used for tumor engrafting experiments is difficult. METHODS: In this study, we developed a tumor engraftment index (TEI) to quantify the immunodeficiency response to hematologic malignant cells and solid tumor cells of six immunodeficient mouse strains and C57BL/6 wild-type mouse (WT). RESULTS: Mice with a more severely impaired immune system attained a higher TEI score. We then validated that the NOD-scid-IL2Rg−/− (NSI) mice, which had the highest TEI score, were more suitable for xenograft and allograft experiments using multiple functional assays. CONCLUSIONS: The TEI score was effectively able to reflect the immunodeficiency of a mouse strain. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13045-015-0156-y) contains supplementary material, which is available to authorized users.