TY - JOUR
T1 - Viral infections in mice with reconstituted human immune system components
AU - Münz, Christian
N1 - Funding Information:
Work in my laboratory is supported by Cancer Research Switzerland ( KFS-3234-08-2013 ), the Association for International Cancer Research ( 11-0516 and 14-1033 ), KFSPMS and KFSPHLD of the University of Zurich , the Baugarten Foundation , the Sobek Foundation , Fondation Acteria , the Wellcome Trust , the Leukaemia and Lymphoma Research , the Medical Research Council and the Swiss National Science Foundation ( 310030_143979 and CRSII3_136241 ).
PY - 2014/9
Y1 - 2014/9
N2 - 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.
AB - 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.
KW - Dengue virus
KW - EBV
KW - HIV
KW - NK cells
KW - T cells
UR - http://www.scopus.com/inward/record.url?scp=84902479310&partnerID=8YFLogxK
U2 - 10.1016/j.imlet.2014.05.012
DO - 10.1016/j.imlet.2014.05.012
M3 - Review article
C2 - 24953718
AN - SCOPUS:84902479310
SN - 0165-2478
VL - 161
SP - 118
EP - 124
JO - Immunology Letters
JF - Immunology Letters
IS - 1
ER -