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Is there an ideal animal model for SARS?

The outbreak of severe acute respiratory syndrome (SARS) in 2003 was controlled by public health measures at a time when specific interventions such as antiviral drugs, vaccines and immunotherapy were not available. Since then, several animal models have been developed for the study of SARS and, alt...

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Detalles Bibliográficos
Autores principales: Subbarao, Kanta, Roberts, Anjeanette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119110/
https://www.ncbi.nlm.nih.gov/pubmed/16759866
http://dx.doi.org/10.1016/j.tim.2006.05.007
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author Subbarao, Kanta
Roberts, Anjeanette
author_facet Subbarao, Kanta
Roberts, Anjeanette
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collection PubMed
description The outbreak of severe acute respiratory syndrome (SARS) in 2003 was controlled by public health measures at a time when specific interventions such as antiviral drugs, vaccines and immunotherapy were not available. Since then, several animal models have been developed for the study of SARS and, although no model replicates the human disease in all aspects, the use of animal models for SARS has led to the establishment of several important principles for vaccine and immunotherapy. Consistency and reproducibility of findings in a given model must be demonstrated to establish the superiority of one model over others. Here, we suggest aspects of an ideal animal model for studies of SARS pathogenesis and vaccine development and present our assessment of the strengths and limitations of the current animal models for SARS.
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spelling pubmed-71191102020-04-03 Is there an ideal animal model for SARS? Subbarao, Kanta Roberts, Anjeanette Trends Microbiol Article The outbreak of severe acute respiratory syndrome (SARS) in 2003 was controlled by public health measures at a time when specific interventions such as antiviral drugs, vaccines and immunotherapy were not available. Since then, several animal models have been developed for the study of SARS and, although no model replicates the human disease in all aspects, the use of animal models for SARS has led to the establishment of several important principles for vaccine and immunotherapy. Consistency and reproducibility of findings in a given model must be demonstrated to establish the superiority of one model over others. Here, we suggest aspects of an ideal animal model for studies of SARS pathogenesis and vaccine development and present our assessment of the strengths and limitations of the current animal models for SARS. Published by Elsevier Ltd. 2006-07 2006-06-08 /pmc/articles/PMC7119110/ /pubmed/16759866 http://dx.doi.org/10.1016/j.tim.2006.05.007 Text en Copyright © 2006 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Subbarao, Kanta
Roberts, Anjeanette
Is there an ideal animal model for SARS?
title Is there an ideal animal model for SARS?
title_full Is there an ideal animal model for SARS?
title_fullStr Is there an ideal animal model for SARS?
title_full_unstemmed Is there an ideal animal model for SARS?
title_short Is there an ideal animal model for SARS?
title_sort is there an ideal animal model for sars?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119110/
https://www.ncbi.nlm.nih.gov/pubmed/16759866
http://dx.doi.org/10.1016/j.tim.2006.05.007
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