Update of humanized animal disease models in studying Graft-versus-host disease

被引:11
作者
Huang, Feng [1 ]
Cao, Feng Lin [2 ]
Zheng, Song Guo [3 ]
机构
[1] Sun Yat Sen Univ, Hosp 3, Dept Clin Immunol, Guangzhou, Guangdong, Peoples R China
[2] Harbin Med Univ, Hosp 1, Hematol Dept, Harbin, Heilongjiang, Peoples R China
[3] Penn State Univ, Milton S Hershey Med Ctr, Dept Med, Hershey, PA 17033 USA
基金
国家重点研发计划;
关键词
Humanized animal models; Autoimmune diseases; Graft-versus-host disease; NOG-SCID mice; HEMATOPOIETIC STEM-CELLS; REGULATORY T-CELLS; HUMAN IMMUNE-SYSTEM; SCID MICE; LONG-TERM; XENOGRAFT MODEL; BLOOD; TRANSPLANTATION; ENGRAFTMENT; MOUSE;
D O I
10.1080/21645515.2018.1512454
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Graft-versus-host disease (GVHD) is a severe adverse effect that results from bone marrow or peripheral blood cells transplantation and has a high rate of mortality. About 50% of the patients are accompanied with acute Graft-versus-Host Disease (aGVHD) after bone marrow cell transplantation and need systematic treatment. It has an important clinical significance to evaluate the prevention and treatment effects of GVHD. The stable and reliable approaches of humanized animal models are crucial for advancing on the study the biology of GVHD. Relative models transplanting the human immune cells into the mouse body can trigger immunoreaction similar to the humans. As it is a disease triggered by human immune cells, any intervention research prior to clinical treatment has more clinical interrelations compared with the general animal models. In this review, we update the current understanding on humanized animal disease models on studying Graft-versus-host disease and expect to provide more theoretical basis to further study on Graft-versus-host disease.
引用
收藏
页码:2618 / 2623
页数:6
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