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Exploiting ovine immunology to improve the relevance of biomedical models

Animal models of human disease are important tools in many areas of biomedicine; for example, in infectious disease research and in the development of novel drugs and medical devices. Most studies involving animals use rodents, in particular congenic mice, due to the availability of a wide number of...

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Detalles Bibliográficos
Autores principales: Entrican, Gary, Wattegedera, Sean R., Griffiths, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368439/
https://www.ncbi.nlm.nih.gov/pubmed/25263932
http://dx.doi.org/10.1016/j.molimm.2014.09.002
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author Entrican, Gary
Wattegedera, Sean R.
Griffiths, David J.
author_facet Entrican, Gary
Wattegedera, Sean R.
Griffiths, David J.
author_sort Entrican, Gary
collection PubMed
description Animal models of human disease are important tools in many areas of biomedicine; for example, in infectious disease research and in the development of novel drugs and medical devices. Most studies involving animals use rodents, in particular congenic mice, due to the availability of a wide number of strains and the ease with which they can be genetically manipulated. The use of mouse models has led to major advances in many fields of research, in particular in immunology but despite these advances, no animal model can exactly reproduce all the features of human disease. It is increasingly becoming recognised that in many circumstances mice do not provide the best model and that alternative species may be more appropriate. Here, we describe the relative merits of sheep as biomedical models for human physiology and disease in comparison to mice, with a particular focus on reproductive and respiratory pathogens.
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spelling pubmed-43684392015-07-01 Exploiting ovine immunology to improve the relevance of biomedical models Entrican, Gary Wattegedera, Sean R. Griffiths, David J. Mol Immunol Article Animal models of human disease are important tools in many areas of biomedicine; for example, in infectious disease research and in the development of novel drugs and medical devices. Most studies involving animals use rodents, in particular congenic mice, due to the availability of a wide number of strains and the ease with which they can be genetically manipulated. The use of mouse models has led to major advances in many fields of research, in particular in immunology but despite these advances, no animal model can exactly reproduce all the features of human disease. It is increasingly becoming recognised that in many circumstances mice do not provide the best model and that alternative species may be more appropriate. Here, we describe the relative merits of sheep as biomedical models for human physiology and disease in comparison to mice, with a particular focus on reproductive and respiratory pathogens. Pergamon Press 2015-07 /pmc/articles/PMC4368439/ /pubmed/25263932 http://dx.doi.org/10.1016/j.molimm.2014.09.002 Text en © The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Entrican, Gary
Wattegedera, Sean R.
Griffiths, David J.
Exploiting ovine immunology to improve the relevance of biomedical models
title Exploiting ovine immunology to improve the relevance of biomedical models
title_full Exploiting ovine immunology to improve the relevance of biomedical models
title_fullStr Exploiting ovine immunology to improve the relevance of biomedical models
title_full_unstemmed Exploiting ovine immunology to improve the relevance of biomedical models
title_short Exploiting ovine immunology to improve the relevance of biomedical models
title_sort exploiting ovine immunology to improve the relevance of biomedical models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368439/
https://www.ncbi.nlm.nih.gov/pubmed/25263932
http://dx.doi.org/10.1016/j.molimm.2014.09.002
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