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Urinary Tract Infection Molecular Mechanisms and Clinical Translation

Rapid developments in infection biology create new and exciting options for individualized diagnostics and therapy. Such new practices are needed to improve patient survival and reduce morbidity. Molecular determinants of host resistance to infection are being characterized, making it possible to id...

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Autores principales: Godaly, Gabriela, Ambite, Ines, Puthia, Manoj, Nadeem, Aftab, Ho, James, Nagy, Karoly, Huang, Yujing, Rydström, Gustav, Svanborg, Catharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810145/
https://www.ncbi.nlm.nih.gov/pubmed/26927188
http://dx.doi.org/10.3390/pathogens5010024
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author Godaly, Gabriela
Ambite, Ines
Puthia, Manoj
Nadeem, Aftab
Ho, James
Nagy, Karoly
Huang, Yujing
Rydström, Gustav
Svanborg, Catharina
author_facet Godaly, Gabriela
Ambite, Ines
Puthia, Manoj
Nadeem, Aftab
Ho, James
Nagy, Karoly
Huang, Yujing
Rydström, Gustav
Svanborg, Catharina
author_sort Godaly, Gabriela
collection PubMed
description Rapid developments in infection biology create new and exciting options for individualized diagnostics and therapy. Such new practices are needed to improve patient survival and reduce morbidity. Molecular determinants of host resistance to infection are being characterized, making it possible to identify susceptible individuals and to predict their risk for future morbidity. Immunotherapy is emerging as a new strategy to treat infections worldwide and controlled boosting of the host immune defense represents an important therapeutic alternative to antibiotics. In proof of concept studies, we have demonstrated that this approach is feasible. The long-term goal is not just to remove the pathogens but to also develop technologies that restore resistance to infection in disease-prone patients and devise personalized therapeutic interventions. Here, we discuss some approaches to reaching these goals, in patients with urinary tract infection (UTI). We describe critical host signaling pathways that define symptoms and pathology and the genetic control of innate immune responses that balance protection against tissue damage. For some of these genes, human relevance has been documented in clinical studies, identifying them as potential targets for immune-modulatory therapies, as a complement to antibiotics.
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spelling pubmed-48101452016-04-04 Urinary Tract Infection Molecular Mechanisms and Clinical Translation Godaly, Gabriela Ambite, Ines Puthia, Manoj Nadeem, Aftab Ho, James Nagy, Karoly Huang, Yujing Rydström, Gustav Svanborg, Catharina Pathogens Review Rapid developments in infection biology create new and exciting options for individualized diagnostics and therapy. Such new practices are needed to improve patient survival and reduce morbidity. Molecular determinants of host resistance to infection are being characterized, making it possible to identify susceptible individuals and to predict their risk for future morbidity. Immunotherapy is emerging as a new strategy to treat infections worldwide and controlled boosting of the host immune defense represents an important therapeutic alternative to antibiotics. In proof of concept studies, we have demonstrated that this approach is feasible. The long-term goal is not just to remove the pathogens but to also develop technologies that restore resistance to infection in disease-prone patients and devise personalized therapeutic interventions. Here, we discuss some approaches to reaching these goals, in patients with urinary tract infection (UTI). We describe critical host signaling pathways that define symptoms and pathology and the genetic control of innate immune responses that balance protection against tissue damage. For some of these genes, human relevance has been documented in clinical studies, identifying them as potential targets for immune-modulatory therapies, as a complement to antibiotics. MDPI 2016-02-24 /pmc/articles/PMC4810145/ /pubmed/26927188 http://dx.doi.org/10.3390/pathogens5010024 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Godaly, Gabriela
Ambite, Ines
Puthia, Manoj
Nadeem, Aftab
Ho, James
Nagy, Karoly
Huang, Yujing
Rydström, Gustav
Svanborg, Catharina
Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title_full Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title_fullStr Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title_full_unstemmed Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title_short Urinary Tract Infection Molecular Mechanisms and Clinical Translation
title_sort urinary tract infection molecular mechanisms and clinical translation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810145/
https://www.ncbi.nlm.nih.gov/pubmed/26927188
http://dx.doi.org/10.3390/pathogens5010024
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