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Genome-Wide Expression Profiling Deciphers Host Responses Altered during Dengue Shock Syndrome and Reveals the Role of Innate Immunity in Severe Dengue

Authors :
Patrich T. Lorn
Veasna Duong
Cédric Sapet
Sina Ngeav
Sivuth Ong
Norith Chroeung
Hugues Tolou
Patricia Couissinier-Paris
Philippe Buchy
Pascal Rihet
Stephanie Devignot
Aurélie Bergon
Institut Pasteur du Cambodge
Réseau International des Instituts Pasteur (RIIP)
Technologies avancées pour le génôme et la clinique (TAGC)
Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Pediatric Department
Kampong Cham Provincial hospital [Cambodia]
Source :
PLoS ONE, PLoS ONE, Public Library of Science, 2010, 5 (7), ⟨10.1371/journal.pone.0011671⟩, PLoS ONE, Vol 5, Iss 7, p e11671 (2010), PLoS ONE, 2010, 5 (7), ⟨10.1371/journal.pone.0011671⟩
Publication Year :
2010
Publisher :
HAL CCSD, 2010.

Abstract

BackgroundDeciphering host responses contributing to dengue shock syndrome (DSS), the life-threatening form of acute viral dengue infections, is required to improve both the differential prognosis and the treatments provided to DSS patients, a challenge for clinicians.Methodology/principal findingsBased on a prospective study, we analyzed the genome-wide expression profiles of whole blood cells from 48 matched Cambodian children: 19 progressed to DSS while 16 and 13 presented respectively classical dengue fever (DF) or dengue hemorrhagic fever grades I/II (DHF). Using multi-way analysis of variance (ANOVA) and adjustment of p-values to control the False Discovery Rate (FDRConclusions/significanceWe provide a global while non exhaustive overview of the molecular mechanisms altered in of DSS children and suggest how they may interact to lead to final vascular homeostasis breakdown. We suggest that some mechanisms identified should be considered putative therapeutic targets or biomarkers of progression to DSS.

Details

Language :
English
ISSN :
19326203
Database :
OpenAIRE
Journal :
PLoS ONE, PLoS ONE, Public Library of Science, 2010, 5 (7), ⟨10.1371/journal.pone.0011671⟩, PLoS ONE, Vol 5, Iss 7, p e11671 (2010), PLoS ONE, 2010, 5 (7), ⟨10.1371/journal.pone.0011671⟩
Accession number :
edsair.doi.dedup.....f36e37a3da2b6ea0584a17668bcdcc9f
Full Text :
https://doi.org/10.1371/journal.pone.0011671⟩