2017
DOI: 10.1016/j.semcdb.2016.07.031
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Peromyscus as a model system for human hepatitis C: An opportunity to advance our understanding of a complex host parasite system

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Cited by 5 publications
(7 citation statements)
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“…They can be divided into two main groups: Animals expressing single antigens or the full viral genome and humanized animals (Section “Humanized animals”) ( Figure 2 C). Animals from the first group usually include those expressing HBsAg [ 103 ], HbcAg [ 104 ], HbeAg [ 105 ], HBx [ 106 ], HCV envelope genes [ 107 ], HCV core [ 108 ] or the full HBV or HCV viral genome [ 109 , 110 , 111 , 112 ].…”
Section: Various In Vivo Approaches In Hepatotropic Virus Modelingmentioning
confidence: 99%
See 1 more Smart Citation
“…They can be divided into two main groups: Animals expressing single antigens or the full viral genome and humanized animals (Section “Humanized animals”) ( Figure 2 C). Animals from the first group usually include those expressing HBsAg [ 103 ], HbcAg [ 104 ], HbeAg [ 105 ], HBx [ 106 ], HCV envelope genes [ 107 ], HCV core [ 108 ] or the full HBV or HCV viral genome [ 109 , 110 , 111 , 112 ].…”
Section: Various In Vivo Approaches In Hepatotropic Virus Modelingmentioning
confidence: 99%
“…They can be divided into two main groups: Animals expressing single antigens or the full viral genome and humanized animals (Section "Humanized animals") (Figure 2C). Animals from the first group usually include those expressing HBsAg [103], HbcAg [104], HbeAg [105], HBx [106], HCV envelope genes [107], HCV core [108] or the full HBV or HCV viral genome [109][110][111][112]. Although transgenic models (usually murine ones) carrying viral genes do not recapitulate several crucial stages of the virus pathogenesis (viral entry, nuclear import, and cccDNA formation), they ensure the virus replication and secretion of viral particles [2], and therefore, can contribute most to the studies on drugs influencing these particular stages.…”
Section: Transgenic Animalsmentioning
confidence: 99%
“…Most research has been carried out in the chimpanzee (Pan troglodytes) model, with important limitations in terms of ethics, small sample sizes, high costs, and genetic heterogeneity (Mesalam et al, 2016), and in the horse model with similar limitations too (Ramsay et al, 2015). Recent models involving chimeric mice with humanized livers and rodent species such as the deer mouse (Peromyscus maniculatus) have improved the situation (Mesalam et al, 2016;Vandegrift et al, 2017). The deer mouse natural model is particularly attractive with the recent discovery of a HCV homolog in this species (Kapoor et al, 2013).…”
Section: Hepatitis C Virusmentioning
confidence: 99%
“…The deer mouse natural model is particularly attractive with the recent discovery of a HCV homolog in this species (Kapoor et al, 2013). These mice are available commercially, develop a spontaneous disease very similar to HCV hepatitis and can serve as natural model to inform about various aspects of this (Vandegrift et al, 2017). There is no pig model to study human HCV infection.…”
Section: Hepatitis C Virusmentioning
confidence: 99%
“…A small animal model based on a naturally occurring virus-host interaction, as has been achieved recently for Norway rat hepacivirus in Norway rats [21], would allow more detailed pathogenesis studies. This would greatly facilitate further research in the development of vaccines [22,23] and novel antivirals [21,24].…”
Section: Introductionmentioning
confidence: 99%