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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...

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Detalles Bibliográficos
Autores principales: Weis, Sebastian, Rubio, Ignacio, Ludwig, Kristin, Weigel, Cynthia, Jentho, Elisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
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.
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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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