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HMGB1 as a drug target in staphylococcal pneumonia

High mobility group box (HMGB)1 is a small DNA-binding protein. In the nucleus, HMGB1 plays a role in gene expression and DNA replication. When it is released or secreted into the extracellular milieu, HMGB1 functions as a pro-inflammatory cytokine-like mediator. Recently reported data support the v...

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Detalles Bibliográficos
Autor principal: Fink, Mitchell P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057072/
https://www.ncbi.nlm.nih.gov/pubmed/25029244
http://dx.doi.org/10.1186/cc13810
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author Fink, Mitchell P
author_facet Fink, Mitchell P
author_sort Fink, Mitchell P
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description High mobility group box (HMGB)1 is a small DNA-binding protein. In the nucleus, HMGB1 plays a role in gene expression and DNA replication. When it is released or secreted into the extracellular milieu, HMGB1 functions as a pro-inflammatory cytokine-like mediator. Recently reported data support the view that treatment with a neutralizing anti-HMGB1 antibody ameliorated pulmonary damage in a murine model of pneumonia caused by a pathogenic strain of Staphylococcus aureus. These findings suggest that HMGB1 may be an important drug target as scientists, clinical investigators and pharmaceutical companies seek to develop better agents for the treatment of staphylococcal pneumonia. Unfortunately, however, encouraging results from murine models of human disease often fail to translate into positive findings in clinical trials. Thus, before moving from pre-clinical into clinical studies, it may be prudent to validate and extend the recent experimental findings by carrying out additional studies, using a large animal model of pneumonia.
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spelling pubmed-40570722015-03-31 HMGB1 as a drug target in staphylococcal pneumonia Fink, Mitchell P Crit Care Commentary High mobility group box (HMGB)1 is a small DNA-binding protein. In the nucleus, HMGB1 plays a role in gene expression and DNA replication. When it is released or secreted into the extracellular milieu, HMGB1 functions as a pro-inflammatory cytokine-like mediator. Recently reported data support the view that treatment with a neutralizing anti-HMGB1 antibody ameliorated pulmonary damage in a murine model of pneumonia caused by a pathogenic strain of Staphylococcus aureus. These findings suggest that HMGB1 may be an important drug target as scientists, clinical investigators and pharmaceutical companies seek to develop better agents for the treatment of staphylococcal pneumonia. Unfortunately, however, encouraging results from murine models of human disease often fail to translate into positive findings in clinical trials. Thus, before moving from pre-clinical into clinical studies, it may be prudent to validate and extend the recent experimental findings by carrying out additional studies, using a large animal model of pneumonia. BioMed Central 2014 2014-03-31 /pmc/articles/PMC4057072/ /pubmed/25029244 http://dx.doi.org/10.1186/cc13810 Text en Copyright © 2014 Fink; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Fink, Mitchell P
HMGB1 as a drug target in staphylococcal pneumonia
title HMGB1 as a drug target in staphylococcal pneumonia
title_full HMGB1 as a drug target in staphylococcal pneumonia
title_fullStr HMGB1 as a drug target in staphylococcal pneumonia
title_full_unstemmed HMGB1 as a drug target in staphylococcal pneumonia
title_short HMGB1 as a drug target in staphylococcal pneumonia
title_sort hmgb1 as a drug target in staphylococcal pneumonia
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057072/
https://www.ncbi.nlm.nih.gov/pubmed/25029244
http://dx.doi.org/10.1186/cc13810
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