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Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential
Due to their inability to generate a complete immune response, mice knockout for type I interferon (IFN) receptors (Ifnar(–/–)) are more susceptible to viral infections, and are thus commonly used for pathogenesis studies. This mouse model has been used to study many diseases caused by highly pathog...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Science Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869239/ https://www.ncbi.nlm.nih.gov/pubmed/29511140 http://dx.doi.org/10.24272/j.issn.2095-8137.2017.052 |
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author | Wong, Gary Qiu, Xiang-Guo |
author_facet | Wong, Gary Qiu, Xiang-Guo |
author_sort | Wong, Gary |
collection | PubMed |
description | Due to their inability to generate a complete immune response, mice knockout for type I interferon (IFN) receptors (Ifnar(–/–)) are more susceptible to viral infections, and are thus commonly used for pathogenesis studies. This mouse model has been used to study many diseases caused by highly pathogenic viruses from many families, including the Flaviviridae, Filoviridae, Arenaviridae, Bunyaviridae, Henipaviridae, and Togaviridae. In this review, we summarize the findings from these animal studies, and discuss the pros and cons of using this model versus other known methods for studying pathogenesis in animals. |
format | Online Article Text |
id | pubmed-5869239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Science Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58692392018-04-12 Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential Wong, Gary Qiu, Xiang-Guo Zool Res Review Due to their inability to generate a complete immune response, mice knockout for type I interferon (IFN) receptors (Ifnar(–/–)) are more susceptible to viral infections, and are thus commonly used for pathogenesis studies. This mouse model has been used to study many diseases caused by highly pathogenic viruses from many families, including the Flaviviridae, Filoviridae, Arenaviridae, Bunyaviridae, Henipaviridae, and Togaviridae. In this review, we summarize the findings from these animal studies, and discuss the pros and cons of using this model versus other known methods for studying pathogenesis in animals. Science Press 2018-02-09 2018-01-18 /pmc/articles/PMC5869239/ /pubmed/29511140 http://dx.doi.org/10.24272/j.issn.2095-8137.2017.052 Text en © 2018. Editorial Office of Zoological Research, Kunming Institute of Zoology, Chinese Academy of Sciences http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Wong, Gary Qiu, Xiang-Guo Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title | Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title_full | Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title_fullStr | Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title_full_unstemmed | Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title_short | Type I interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
title_sort | type i interferon receptor knockout mice as models for infection of highly pathogenic viruses with outbreak potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869239/ https://www.ncbi.nlm.nih.gov/pubmed/29511140 http://dx.doi.org/10.24272/j.issn.2095-8137.2017.052 |
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