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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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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. |
format | Online Article Text |
id | pubmed-4810145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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