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- Publisher Website: 10.1186/s13045-015-0156-y
- Scopus: eid_2-s2.0-84934906688
- PMID: 26022250
- WOS: WOS:000356772000001
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Article: Quantitative evaluation of the immunodeficiency of a mouse strain by tumor engraftments
Title | Quantitative evaluation of the immunodeficiency of a mouse strain by tumor engraftments |
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Authors | |
Keywords | Tumor Immunodeficiency Allograft Xenograft Leukemia |
Issue Date | 2015 |
Citation | Journal of Hematology and Oncology, 2015, v. 8, n. 1 How to Cite? |
Abstract | © 2015 Ye et al. 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. |
Persistent Identifier | http://hdl.handle.net/10722/249151 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ye, Wei | - |
dc.contributor.author | Jiang, Zhiwu | - |
dc.contributor.author | Li, Guan Xiong | - |
dc.contributor.author | Xiao, Yiren | - |
dc.contributor.author | Lin, Simiao | - |
dc.contributor.author | Lai, Yunxin | - |
dc.contributor.author | Wang, Suna | - |
dc.contributor.author | Li, Baiheng | - |
dc.contributor.author | Jia, Bei | - |
dc.contributor.author | Li, Yin | - |
dc.contributor.author | Huang, Zhi Liang | - |
dc.contributor.author | Li, Jin | - |
dc.contributor.author | Feng, Fenglan | - |
dc.contributor.author | Li, Shuhua | - |
dc.contributor.author | Yao, Huihui | - |
dc.contributor.author | Liu, Zixia | - |
dc.contributor.author | Cao, Su | - |
dc.contributor.author | Xu, Lin | - |
dc.contributor.author | Li, Yangqiu | - |
dc.contributor.author | Wu, Donghai | - |
dc.contributor.author | Zeng, Lingwen | - |
dc.contributor.author | Zhong, Mei | - |
dc.contributor.author | Liu, Pentao | - |
dc.contributor.author | Wen, Zhe Sheng | - |
dc.contributor.author | Xu, Bing | - |
dc.contributor.author | Yao, Yao | - |
dc.contributor.author | Pei, Duanqing | - |
dc.contributor.author | Li, Peng | - |
dc.date.accessioned | 2017-10-27T05:59:14Z | - |
dc.date.available | 2017-10-27T05:59:14Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | Journal of Hematology and Oncology, 2015, v. 8, n. 1 | - |
dc.identifier.uri | http://hdl.handle.net/10722/249151 | - |
dc.description.abstract | © 2015 Ye et al. 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. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Hematology and Oncology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Tumor | - |
dc.subject | Immunodeficiency | - |
dc.subject | Allograft | - |
dc.subject | Xenograft | - |
dc.subject | Leukemia | - |
dc.title | Quantitative evaluation of the immunodeficiency of a mouse strain by tumor engraftments | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/s13045-015-0156-y | - |
dc.identifier.pmid | 26022250 | - |
dc.identifier.scopus | eid_2-s2.0-84934906688 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | null | - |
dc.identifier.epage | null | - |
dc.identifier.eissn | 1756-8722 | - |
dc.identifier.isi | WOS:000356772000001 | - |
dc.identifier.issnl | 1756-8722 | - |