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Hormesis and Defense of Infectious Disease
Infectious diseases are a global health burden and remain associated with high social and economic impact. Treatment of affected patients largely relies on antimicrobial agents that act by directly targeting microbial replication. Despite the utility of host specific therapies having been assessed i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486095/ https://www.ncbi.nlm.nih.gov/pubmed/28617331 http://dx.doi.org/10.3390/ijms18061273 |
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author | Weis, Sebastian Rubio, Ignacio Ludwig, Kristin Weigel, Cynthia Jentho, Elisa |
author_facet | Weis, Sebastian Rubio, Ignacio Ludwig, Kristin Weigel, Cynthia Jentho, Elisa |
author_sort | Weis, Sebastian |
collection | PubMed |
description | Infectious diseases are a global health burden and remain associated with high social and economic impact. Treatment of affected patients largely relies on antimicrobial agents that act by directly targeting microbial replication. Despite the utility of host specific therapies having been assessed in previous clinical trials, such as targeting the immune response via modulating the cytokine release in sepsis, results have largely been frustrating and did not lead to the introduction of new therapeutic tools. In this article, we will discuss current evidence arguing that, by applying the concept of hormesis, already approved pharmacological agents could be used therapeutically to increase survival of patients with infectious disease via improving disease tolerance, a defense mechanism that decreases the extent of infection-associated tissue damage without directly targeting pathogenic microorganisms. |
format | Online Article Text |
id | pubmed-5486095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-54860952017-06-29 Hormesis and Defense of Infectious Disease Weis, Sebastian Rubio, Ignacio Ludwig, Kristin Weigel, Cynthia Jentho, Elisa Int J Mol Sci Review Infectious diseases are a global health burden and remain associated with high social and economic impact. Treatment of affected patients largely relies on antimicrobial agents that act by directly targeting microbial replication. Despite the utility of host specific therapies having been assessed in previous clinical trials, such as targeting the immune response via modulating the cytokine release in sepsis, results have largely been frustrating and did not lead to the introduction of new therapeutic tools. In this article, we will discuss current evidence arguing that, by applying the concept of hormesis, already approved pharmacological agents could be used therapeutically to increase survival of patients with infectious disease via improving disease tolerance, a defense mechanism that decreases the extent of infection-associated tissue damage without directly targeting pathogenic microorganisms. MDPI 2017-06-15 /pmc/articles/PMC5486095/ /pubmed/28617331 http://dx.doi.org/10.3390/ijms18061273 Text en © 2017 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 Weis, Sebastian Rubio, Ignacio Ludwig, Kristin Weigel, Cynthia Jentho, Elisa Hormesis and Defense of Infectious Disease |
title | Hormesis and Defense of Infectious Disease |
title_full | Hormesis and Defense of Infectious Disease |
title_fullStr | Hormesis and Defense of Infectious Disease |
title_full_unstemmed | Hormesis and Defense of Infectious Disease |
title_short | Hormesis and Defense of Infectious Disease |
title_sort | hormesis and defense of infectious disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486095/ https://www.ncbi.nlm.nih.gov/pubmed/28617331 http://dx.doi.org/10.3390/ijms18061273 |
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