Literature DB >> 24216294

Association between proinflammatory cytokines and lipid peroxidation in patients with severe dengue disease around defervescence.

R Soundravally1, S L Hoti2, Shripad A Patil3, C C Cleetus4, Bobby Zachariah4, T Kadhiravan4, P Narayanan4, B Agiesh Kumar5.   

Abstract

OBJECTIVES: Proinflammatory cytokines and the oxidative stress response are reported to be involved in dengue viral disease. The present study investigated the correlation of proinflammatory cytokines and lipid peroxidation with dengue severity.
METHODS: Clinical samples from 27 dengue fever (DF) cases, 30 dengue haemorrhagic fever (DHF) cases, and 24 dengue shock syndrome (DSS) cases were studied around defervescence, along with samples from 30 healthy controls. Plasma samples were analysed for tumour necrosis factor alpha (TNF-α) and interferon gamma (IFN-γ) by ELISA and for malondialdehyde (MDA) by thiobarbituric acid assay.
RESULTS: Dengue-infected individuals had significantly higher levels of TNF-α, IFN-γ, and MDA in comparison to controls. The ratio of TNF-α to IFN-γ was significantly higher in DHF and DSS than in DF. A TNF-α/IFN-γ ratio value of 5.69 around defervescence predicted DHF and DSS with moderate accuracy and thus may serve as an indicator to study dengue severity. The study observed a significant positive correlation of lipid peroxides with TNF-α levels and the TNF-α/IFN-γ ratio in severe dengue cases.
CONCLUSIONS: We propose that the oxidative stress response induced by the dengue virus may trigger the inflammatory cytokine responses in dengue severity and thereby contributes to the pathogenesis of the disease; however the interplay between the oxidative response and inflammatory activity in disease virulence needs further study.
Copyright © 2013 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  DHF; DSS; Lipid peroxides; Malondialdehyde; Proinflammatory cytokine; TNF-α/IFN-γ ratio

Mesh:

Substances:

Year:  2013        PMID: 24216294     DOI: 10.1016/j.ijid.2013.09.022

Source DB:  PubMed          Journal:  Int J Infect Dis        ISSN: 1201-9712            Impact factor:   3.623


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