Koyanagi Y, Tanaka Y, Ito M, Yamamoto N
Laboratory of Viral Pathogenesis, Institute for Virus Research, Kyoto University, 53 Shougoinkawara cho, Sakyou-ku, Kyoto 606-8507, Japan.
Curr Top Microbiol Immunol. 2008;324:133-48. doi: 10.1007/978-3-540-75647-7_9.
Inbred mice with specific genetic defects have greatly facilitated the analysis of complex biological events. Several humanized mouse models using the C.B.-17 scid/scid mouse (referred to as the SCID mouse) have been created from two transplantation protocols, and these mice have been utilized for the investigation of human immunodeficiency virus type 1 (HIV-1) and human T-lymphotropic virus type I (HTLV-I) pathogenesis and the evaluation of antiviral compounds. To generate a more prominent small animal model for human retrovirus infection, especially for examination of the pathological process and the immune reaction, a novel immunodeficient mouse strain derived from the NOD SCID mouse was created by backcrossing with a common gamma chain (gamma(c))-knockout mouse. The NOD-SCID gamma(c)null (NOG) mouse has neither functional T and B cells nor NK cells and has been used as a recipient in humanized mouse models for transplantation of human immune cells particularly including hematopoietic stem cells (HSC). From recent advances in development of humanized mice, we are now able to provide a new version of the animal model for human retrovirus infection and human immunity.
具有特定基因缺陷的近交系小鼠极大地促进了对复杂生物事件的分析。通过两种移植方案创建了几种使用C.B.-17 scid/scid小鼠(称为SCID小鼠)的人源化小鼠模型,这些小鼠已被用于研究1型人类免疫缺陷病毒(HIV-1)和I型人类嗜T淋巴细胞病毒(HTLV-I)的发病机制以及评估抗病毒化合物。为了生成一个更突出的用于人类逆转录病毒感染的小动物模型,特别是用于检查病理过程和免疫反应,通过与常见γ链(γ(c))敲除小鼠回交,从NOD SCID小鼠培育出一种新型免疫缺陷小鼠品系。NOD-SCID γ(c)缺失(NOG)小鼠既没有功能性T细胞和B细胞,也没有NK细胞,已被用作人源化小鼠模型中人类免疫细胞特别是造血干细胞(HSC)移植的受体。根据人源化小鼠开发的最新进展,我们现在能够提供一种用于人类逆转录病毒感染和人类免疫的新型动物模型。