Infectious diseases in humanized mice

被引:41
|
作者
Leung, Carol [1 ]
Chijioke, Obinna [1 ]
Gujer, Cornelia [1 ]
Chatterjee, Bithi [1 ]
Antsiferova, Olga [1 ]
Landtwing, Vanessa [1 ]
McHugh, Donal [1 ]
Raykova, Ana [1 ]
Muenz, Christian [1 ]
机构
[1] Univ Zurich, Inst Expt Immunol, Dept Viral Immunobiol, CH-8057 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Dengue virus; EBV; HIV; Mycobacterium tuberculosis; Salmonella enterica typhi; BARR-VIRUS INFECTION; HUMAN IMMUNE-SYSTEM; SCID IL2R-GAMMA(NULL) MICE; REGULATORY PROTEIN ALPHA; T-CELL RESPONSES; HIV-1; INFECTION; MOUSE MODEL; MUCOSAL TRANSMISSION; BLOOD; ENGRAFTMENT;
D O I
10.1002/eji.201343815
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite many theoretical incompatibilities between mouse and human cells, mice with reconstituted human immune system components contain nearly all human leukocyte populations. Accordingly, several human-tropic pathogens have been investigated in these in vivo models of the human immune system, including viruses such as human immunodeficiency virus (HIV) and Epstein-Barr virus (EBV), as well as bacteria such as Mycobacterium tuberculosis and Salmonella enterica Typhi. While these studies initially aimed to establish similarities in the pathogenesis of infections between these models and the pathobiology in patients, recent investigations have provided new and interesting functional insights into the protective value of certain immune compartments and altered pathology upon mutant pathogen infections. As more tools and methodologies are developed to make these models more versatile to study human immune responses in vivo, such improvements build toward small animal models with human immune components, which could predict immune responses to therapies and vaccination in human patients.
引用
收藏
页码:2246 / 2254
页数:9
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