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Increased neutrophil apoptosis in chronically SIV-infected macaques

Polymorphonuclear neutrophils (PMN) from chronically HIV-infected individuals have been reported to be more prone to die. However, although non-human primates models have been extensively used for improving our knowledge on T cell immunity, the impact of SIV-infection on PMN, in relationships with d...

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Autores principales: Elbim, Carole, Monceaux, Valérie, François, Stéphanie, Hurtrel, Bruno, Gougerot-Pocidalo, Marie-Anne, Estaquier, Jérome
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667475/
https://www.ncbi.nlm.nih.gov/pubmed/19317901
http://dx.doi.org/10.1186/1742-4690-6-29
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author Elbim, Carole
Monceaux, Valérie
François, Stéphanie
Hurtrel, Bruno
Gougerot-Pocidalo, Marie-Anne
Estaquier, Jérome
author_facet Elbim, Carole
Monceaux, Valérie
François, Stéphanie
Hurtrel, Bruno
Gougerot-Pocidalo, Marie-Anne
Estaquier, Jérome
author_sort Elbim, Carole
collection PubMed
description Polymorphonuclear neutrophils (PMN) from chronically HIV-infected individuals have been reported to be more prone to die. However, although non-human primates models have been extensively used for improving our knowledge on T cell immunity, the impact of SIV-infection on PMN, in relationships with disease severity, has never been assessed. In our study, we demonstrate that PMN from Rhesus macaques (RMs) of Chinese origin chronically infected with the virulent strain SIVmac251 display increased susceptibility to undergo apoptosis as compared to PMN from RMs infected with the non-pathogenic SIVΔnef strain. PMN apoptosis was significantly increased in RMs progressing faster to AIDS as compared to non-progressors RMs. Furthermore, the percentage of apoptotic cells correlated with PMN activation state reflected by increased CD11b expression and reactive oxygen species production. Interestingly, whereas inflammatory cytokines IL-8 and IL-1β prevent in vitro PMN death, the levels of those cytokines were low in RMs progressing towards AIDS. Altogether, increased PMN death during SIV infection is a new pathogenic effect associated with AIDS progression, adding to the long list of markers associated with disruption of defense against infection.
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spelling pubmed-26674752009-04-10 Increased neutrophil apoptosis in chronically SIV-infected macaques Elbim, Carole Monceaux, Valérie François, Stéphanie Hurtrel, Bruno Gougerot-Pocidalo, Marie-Anne Estaquier, Jérome Retrovirology Short Report Polymorphonuclear neutrophils (PMN) from chronically HIV-infected individuals have been reported to be more prone to die. However, although non-human primates models have been extensively used for improving our knowledge on T cell immunity, the impact of SIV-infection on PMN, in relationships with disease severity, has never been assessed. In our study, we demonstrate that PMN from Rhesus macaques (RMs) of Chinese origin chronically infected with the virulent strain SIVmac251 display increased susceptibility to undergo apoptosis as compared to PMN from RMs infected with the non-pathogenic SIVΔnef strain. PMN apoptosis was significantly increased in RMs progressing faster to AIDS as compared to non-progressors RMs. Furthermore, the percentage of apoptotic cells correlated with PMN activation state reflected by increased CD11b expression and reactive oxygen species production. Interestingly, whereas inflammatory cytokines IL-8 and IL-1β prevent in vitro PMN death, the levels of those cytokines were low in RMs progressing towards AIDS. Altogether, increased PMN death during SIV infection is a new pathogenic effect associated with AIDS progression, adding to the long list of markers associated with disruption of defense against infection. BioMed Central 2009-03-24 /pmc/articles/PMC2667475/ /pubmed/19317901 http://dx.doi.org/10.1186/1742-4690-6-29 Text en Copyright © 2009 Elbim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Elbim, Carole
Monceaux, Valérie
François, Stéphanie
Hurtrel, Bruno
Gougerot-Pocidalo, Marie-Anne
Estaquier, Jérome
Increased neutrophil apoptosis in chronically SIV-infected macaques
title Increased neutrophil apoptosis in chronically SIV-infected macaques
title_full Increased neutrophil apoptosis in chronically SIV-infected macaques
title_fullStr Increased neutrophil apoptosis in chronically SIV-infected macaques
title_full_unstemmed Increased neutrophil apoptosis in chronically SIV-infected macaques
title_short Increased neutrophil apoptosis in chronically SIV-infected macaques
title_sort increased neutrophil apoptosis in chronically siv-infected macaques
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667475/
https://www.ncbi.nlm.nih.gov/pubmed/19317901
http://dx.doi.org/10.1186/1742-4690-6-29
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