作者
Cornelia AM van de Weg, Cláudio S Pannuti, Evaldo SA de Araujo, Henk-Jan van den Ham, Arno C Andeweg, Lucy SV Boas, Alvina C Felix, Karina I Carvalho, Andreia M de Matos, José E Levi, Camila M Romano, Cristiane C Centrone, Celia L de Lima Rodrigues, Expedito Luna, Eric CM van Gorp, Albert DME Osterhaus, Byron EE Martina, Esper G Kallas
发表日期
2013/5/23
期刊
PLoS neglected tropical diseases
卷号
7
期号
5
页码范围
e2236
出版商
Public Library of Science
简介
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 …
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CAM van de Weg, CS Pannuti, ESA de Araujo… - PLoS neglected tropical diseases, 2013