Viral infections in mice with reconstituted human immune system components

被引:4
|
作者
Muenz, Christian [1 ]
机构
[1] Univ Zurich, Inst Expt Immunol, CH-8006 Zurich, Switzerland
基金
瑞士国家科学基金会; 英国医学研究理事会; 英国惠康基金;
关键词
HIV; EBV; Dengue virus; NK cells; T cells; EPSTEIN-BARR-VIRUS; REGULATORY PROTEIN ALPHA; HUMAN CD34(+) CELLS; CD4(+) T-CELLS; HIV-1; INFECTION; MOUSE MODEL; ANIMAL-MODEL; RESPONSES; GENERATION; DIFFERENTIATION;
D O I
10.1016/j.imlet.2014.05.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pathogenic viruses are often difficult to study due to their exclusive tropism for humans. The development of mice with human immune system components opens the possibility to study those human pathogens with a tropism for the human hematopoietic lineage in vivo. These include HCMV, EBV, KSHV, HIV, HTLV-1, dengue virus and JC virus. Furthermore, some human pathogens, like HSV-2, adenovirus, HCV, HBV and influenza A virus, with an additional tropism for somatic mouse tissues or for additional transplanted human tissues, mainly liver, have been explored in these models. The cellular tropism of these viruses, their associated diseases and primarily cell-mediated immune responses to these viral infections will be discussed in this review. Already some exciting information has been gained from these novel chimeric in vivo models and future avenues to gain more insights into the pathology, but also potential therapies, will be outlined. Although the respective in vivo models of human immune responses can still be significantly improved, they already provide preclinical systems for in vivo studies of important viral pathogens of humans. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 124
页数:7
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