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Effect of NMSO3 treatment in a murine model of human metapneumovirus infection
BALB/c mice infected with human metapneumovirus (hMPV) were treated with the sulfated sialyl lipid NMSO3 (one dose of 50 mg kg(−1)) given at the time of infection. NMSO3 significantly reduced viral replication in the lungs, as well as hMPV-induced body weight loss, pulmonary inflammation and cytokin...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Society for General Microbiology
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800786/ https://www.ncbi.nlm.nih.gov/pubmed/18931066 http://dx.doi.org/10.1099/vir.0.2008/003301-0 |
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author | Spetch, Leanne Bowlin, Terry L. Casola, Antonella |
author_facet | Spetch, Leanne Bowlin, Terry L. Casola, Antonella |
author_sort | Spetch, Leanne |
collection | PubMed |
description | BALB/c mice infected with human metapneumovirus (hMPV) were treated with the sulfated sialyl lipid NMSO3 (one dose of 50 mg kg(−1)) given at the time of infection. NMSO3 significantly reduced viral replication in the lungs, as well as hMPV-induced body weight loss, pulmonary inflammation and cytokine production, suggesting that antiviral treatment initiated at the beginning of viral infection can modify hMPV-induced disease. |
format | Text |
id | pubmed-2800786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Society for General Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-28007862009-12-31 Effect of NMSO3 treatment in a murine model of human metapneumovirus infection Spetch, Leanne Bowlin, Terry L. Casola, Antonella J Gen Virol Animal BALB/c mice infected with human metapneumovirus (hMPV) were treated with the sulfated sialyl lipid NMSO3 (one dose of 50 mg kg(−1)) given at the time of infection. NMSO3 significantly reduced viral replication in the lungs, as well as hMPV-induced body weight loss, pulmonary inflammation and cytokine production, suggesting that antiviral treatment initiated at the beginning of viral infection can modify hMPV-induced disease. Society for General Microbiology 2008-11 /pmc/articles/PMC2800786/ /pubmed/18931066 http://dx.doi.org/10.1099/vir.0.2008/003301-0 Text en Copyright © 2008, SGM http://creativecommons.org/licenses/by/2.5/ 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 work is properly cited. |
spellingShingle | Animal Spetch, Leanne Bowlin, Terry L. Casola, Antonella Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title | Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title_full | Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title_fullStr | Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title_full_unstemmed | Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title_short | Effect of NMSO3 treatment in a murine model of human metapneumovirus infection |
title_sort | effect of nmso3 treatment in a murine model of human metapneumovirus infection |
topic | Animal |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800786/ https://www.ncbi.nlm.nih.gov/pubmed/18931066 http://dx.doi.org/10.1099/vir.0.2008/003301-0 |
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