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The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research

Human immune system (HIS) mice are a subset of humanized mice that are generated by xenoengraftment of human immune cells or tissues and/or their progenitors into immunodeficient mice. Viral hemorrhagic fevers (VHFs) cause severe disease in humans, typically with high case fatality rates. HIS mouse...

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Autores principales: Wozniak, David M., Lavender, Kerry J., Prescott, Joseph, Spengler, Jessica R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157695/
https://www.ncbi.nlm.nih.gov/pubmed/32098330
http://dx.doi.org/10.3390/vaccines8010098
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author Wozniak, David M.
Lavender, Kerry J.
Prescott, Joseph
Spengler, Jessica R.
author_facet Wozniak, David M.
Lavender, Kerry J.
Prescott, Joseph
Spengler, Jessica R.
author_sort Wozniak, David M.
collection PubMed
description Human immune system (HIS) mice are a subset of humanized mice that are generated by xenoengraftment of human immune cells or tissues and/or their progenitors into immunodeficient mice. Viral hemorrhagic fevers (VHFs) cause severe disease in humans, typically with high case fatality rates. HIS mouse studies have been performed to investigate the pathogenesis and immune responses to VHFs that must be handled in high-containment laboratory facilities. Here, we summarize studies on filoviruses, nairoviruses, phenuiviruses, and hantaviruses, and discuss the knowledge gained from using various HIS mouse models. Furthermore, we discuss the complexities of designing and interpreting studies utilizing HIS mice while highlighting additional questions about VHFs that can still be addressed using HIS mouse models.
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spelling pubmed-71576952020-04-21 The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research Wozniak, David M. Lavender, Kerry J. Prescott, Joseph Spengler, Jessica R. Vaccines (Basel) Review Human immune system (HIS) mice are a subset of humanized mice that are generated by xenoengraftment of human immune cells or tissues and/or their progenitors into immunodeficient mice. Viral hemorrhagic fevers (VHFs) cause severe disease in humans, typically with high case fatality rates. HIS mouse studies have been performed to investigate the pathogenesis and immune responses to VHFs that must be handled in high-containment laboratory facilities. Here, we summarize studies on filoviruses, nairoviruses, phenuiviruses, and hantaviruses, and discuss the knowledge gained from using various HIS mouse models. Furthermore, we discuss the complexities of designing and interpreting studies utilizing HIS mice while highlighting additional questions about VHFs that can still be addressed using HIS mouse models. MDPI 2020-02-22 /pmc/articles/PMC7157695/ /pubmed/32098330 http://dx.doi.org/10.3390/vaccines8010098 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wozniak, David M.
Lavender, Kerry J.
Prescott, Joseph
Spengler, Jessica R.
The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title_full The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title_fullStr The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title_full_unstemmed The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title_short The Utility of Human Immune System Mice for High-Containment Viral Hemorrhagic Fever Research
title_sort utility of human immune system mice for high-containment viral hemorrhagic fever research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7157695/
https://www.ncbi.nlm.nih.gov/pubmed/32098330
http://dx.doi.org/10.3390/vaccines8010098
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