Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.

Changes in immune response during lifespan of man are well known. These changes involve decreased neonatal and elderly immune response. In addition, it has been shown a relationship between immune and oxidative mechanisms, suggesting that altered immune response could be associated to altered oxidat...

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Main Authors: Nereida Valero, Jesús Mosquera, Germán Añez, Alegria Levy, Rafael Marcucci, Melchor Alvarez de Mon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24069178/pdf/?tool=EBI
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spelling doaj-926241627ab340a3b6e00c2bcee7bea22021-03-03T22:52:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7322110.1371/journal.pone.0073221Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.Nereida ValeroJesús MosqueraGermán AñezAlegria LevyRafael MarcucciMelchor Alvarez de MonChanges in immune response during lifespan of man are well known. These changes involve decreased neonatal and elderly immune response. In addition, it has been shown a relationship between immune and oxidative mechanisms, suggesting that altered immune response could be associated to altered oxidative response. Increased expression of nitric oxide (NO) has been documented in dengue and in monocyte cultures infected with different types of dengue virus. However, there is no information about the age-dependent NO oxidative response in humans infected by dengue virus. In this study, monocyte cultures from neonatal, elderly and adult individuals (n = 10 each group) were infected with different dengue virus types (DENV- 1 to 4) and oxidative/antioxidative responses and apoptosis were measured at days 1 and 3 of culture. Increased production of NO, lipid peroxidation and enzymatic and nonenzymatic anti-oxidative responses in dengue infected monocyte cultures were observed. However, neonatal and elderly monocytes had lower values of studied parameters when compared to those in adult-derived cultures. Apoptosis was present in infected monocytes with higher values at day 3 of culture. This reduced oxidant/antioxidant response of neonatal and elderly monocytes could be relevant in the pathogenesis of dengue disease.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24069178/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Nereida Valero
Jesús Mosquera
Germán Añez
Alegria Levy
Rafael Marcucci
Melchor Alvarez de Mon
spellingShingle Nereida Valero
Jesús Mosquera
Germán Añez
Alegria Levy
Rafael Marcucci
Melchor Alvarez de Mon
Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
PLoS ONE
author_facet Nereida Valero
Jesús Mosquera
Germán Añez
Alegria Levy
Rafael Marcucci
Melchor Alvarez de Mon
author_sort Nereida Valero
title Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
title_short Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
title_full Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
title_fullStr Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
title_full_unstemmed Differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
title_sort differential oxidative stress induced by dengue virus in monocytes from human neonates, adult and elderly individuals.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Changes in immune response during lifespan of man are well known. These changes involve decreased neonatal and elderly immune response. In addition, it has been shown a relationship between immune and oxidative mechanisms, suggesting that altered immune response could be associated to altered oxidative response. Increased expression of nitric oxide (NO) has been documented in dengue and in monocyte cultures infected with different types of dengue virus. However, there is no information about the age-dependent NO oxidative response in humans infected by dengue virus. In this study, monocyte cultures from neonatal, elderly and adult individuals (n = 10 each group) were infected with different dengue virus types (DENV- 1 to 4) and oxidative/antioxidative responses and apoptosis were measured at days 1 and 3 of culture. Increased production of NO, lipid peroxidation and enzymatic and nonenzymatic anti-oxidative responses in dengue infected monocyte cultures were observed. However, neonatal and elderly monocytes had lower values of studied parameters when compared to those in adult-derived cultures. Apoptosis was present in infected monocytes with higher values at day 3 of culture. This reduced oxidant/antioxidant response of neonatal and elderly monocytes could be relevant in the pathogenesis of dengue disease.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24069178/pdf/?tool=EBI
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