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Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease
BACKGROUND: Severe dengue virus (DENV) disease is associated with extensive immune activation, characterized by a cytokine storm. Previously, elevated lipopolysaccharide (LPS) levels in dengue were found to correlate with clinical disease severity. In the present cross-sectional study we identified...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662706/ https://www.ncbi.nlm.nih.gov/pubmed/23717702 http://dx.doi.org/10.1371/journal.pntd.0002236 |
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author | van de Weg, Cornelia A. M. Pannuti, Cláudio S. de Araújo, Evaldo S. A. van den Ham, Henk-Jan Andeweg, Arno C. Boas, Lucy S. V. Felix, Alvina C. Carvalho, Karina I. de Matos, Andreia M. Levi, José E. Romano, Camila M. Centrone, Cristiane C. de Lima Rodrigues, Celia L. Luna, Expedito van Gorp, Eric C. M. Osterhaus, Albert D. M. E. Martina, Byron E. E. Kallas, Esper G. |
author_facet | van de Weg, Cornelia A. M. Pannuti, Cláudio S. de Araújo, Evaldo S. A. van den Ham, Henk-Jan Andeweg, Arno C. Boas, Lucy S. V. Felix, Alvina C. Carvalho, Karina I. de Matos, Andreia M. Levi, José E. Romano, Camila M. Centrone, Cristiane C. de Lima Rodrigues, Celia L. Luna, Expedito van Gorp, Eric C. M. Osterhaus, Albert D. M. E. Martina, Byron E. E. Kallas, Esper G. |
author_sort | van de Weg, Cornelia A. M. |
collection | PubMed |
description | BACKGROUND: Severe dengue virus (DENV) disease is associated with extensive immune activation, characterized by a cytokine storm. Previously, elevated lipopolysaccharide (LPS) levels in dengue were found to correlate with clinical disease severity. In the present cross-sectional study we identified markers of microbial translocation and immune activation, which are associated with severe manifestations of DENV infection. METHODS: Serum samples from DENV-infected patients were collected during the outbreak in 2010 in the State of São Paulo, Brazil. Levels of LPS, lipopolysaccharide binding protein (LBP), soluble CD14 (sCD14) and IgM and IgG endotoxin core antibodies were determined by ELISA. Thirty cytokines were quantified using a multiplex luminex system. Patients were classified according to the 2009 WHO classification and the occurrence of plasma leakage/shock and hemorrhage. Moreover, a (non-supervised) cluster analysis based on the expression of the quantified cytokines was applied to identify groups of patients with similar cytokine profiles. Markers of microbial translocation were linked to groups with similar clinical disease severity and clusters with similar cytokine profiles. RESULTS: Cluster analysis indicated that LPS levels were significantly increased in patients with a profound pro-inflammatory cytokine profile. LBP and sCD14 showed significantly increased levels in patients with severe disease in the clinical classification and in patients with severe inflammation in the cluster analysis. With both the clinical classification and the cluster analysis, levels of IL-6, IL-8, sIL-2R, MCP-1, RANTES, HGF, G-CSF and EGF were associated with severe disease. CONCLUSIONS: The present study provides evidence that both microbial translocation and extensive immune activation occur during severe DENV infection and may play an important role in the pathogenesis. |
format | Online Article Text |
id | pubmed-3662706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36627062013-05-28 Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease van de Weg, Cornelia A. M. Pannuti, Cláudio S. de Araújo, Evaldo S. A. van den Ham, Henk-Jan Andeweg, Arno C. Boas, Lucy S. V. Felix, Alvina C. Carvalho, Karina I. de Matos, Andreia M. Levi, José E. Romano, Camila M. Centrone, Cristiane C. de Lima Rodrigues, Celia L. Luna, Expedito van Gorp, Eric C. M. Osterhaus, Albert D. M. E. Martina, Byron E. E. Kallas, Esper G. PLoS Negl Trop Dis Research Article BACKGROUND: Severe dengue virus (DENV) disease is associated with extensive immune activation, characterized by a cytokine storm. Previously, elevated lipopolysaccharide (LPS) levels in dengue were found to correlate with clinical disease severity. In the present cross-sectional study we identified markers of microbial translocation and immune activation, which are associated with severe manifestations of DENV infection. METHODS: Serum samples from DENV-infected patients were collected during the outbreak in 2010 in the State of São Paulo, Brazil. Levels of LPS, lipopolysaccharide binding protein (LBP), soluble CD14 (sCD14) and IgM and IgG endotoxin core antibodies were determined by ELISA. Thirty cytokines were quantified using a multiplex luminex system. Patients were classified according to the 2009 WHO classification and the occurrence of plasma leakage/shock and hemorrhage. Moreover, a (non-supervised) cluster analysis based on the expression of the quantified cytokines was applied to identify groups of patients with similar cytokine profiles. Markers of microbial translocation were linked to groups with similar clinical disease severity and clusters with similar cytokine profiles. RESULTS: Cluster analysis indicated that LPS levels were significantly increased in patients with a profound pro-inflammatory cytokine profile. LBP and sCD14 showed significantly increased levels in patients with severe disease in the clinical classification and in patients with severe inflammation in the cluster analysis. With both the clinical classification and the cluster analysis, levels of IL-6, IL-8, sIL-2R, MCP-1, RANTES, HGF, G-CSF and EGF were associated with severe disease. CONCLUSIONS: The present study provides evidence that both microbial translocation and extensive immune activation occur during severe DENV infection and may play an important role in the pathogenesis. Public Library of Science 2013-05-23 /pmc/articles/PMC3662706/ /pubmed/23717702 http://dx.doi.org/10.1371/journal.pntd.0002236 Text en © 2013 van de Weg et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article van de Weg, Cornelia A. M. Pannuti, Cláudio S. de Araújo, Evaldo S. A. van den Ham, Henk-Jan Andeweg, Arno C. Boas, Lucy S. V. Felix, Alvina C. Carvalho, Karina I. de Matos, Andreia M. Levi, José E. Romano, Camila M. Centrone, Cristiane C. de Lima Rodrigues, Celia L. Luna, Expedito van Gorp, Eric C. M. Osterhaus, Albert D. M. E. Martina, Byron E. E. Kallas, Esper G. Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title | Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title_full | Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title_fullStr | Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title_full_unstemmed | Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title_short | Microbial Translocation Is Associated with Extensive Immune Activation in Dengue Virus Infected Patients with Severe Disease |
title_sort | microbial translocation is associated with extensive immune activation in dengue virus infected patients with severe disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662706/ https://www.ncbi.nlm.nih.gov/pubmed/23717702 http://dx.doi.org/10.1371/journal.pntd.0002236 |
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