Cargando…
Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection
Chronic immune activation and progression to AIDS are observed after SIV infection in macaques but not in natural host primate species. To better understand this dichotomy, we compared acute pathogenic SIV infection in pigtailed macaques (PTs) to non-pathogenic infection in African green monkeys (AG...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635016/ https://www.ncbi.nlm.nih.gov/pubmed/19214220 http://dx.doi.org/10.1371/journal.ppat.1000295 |
_version_ | 1782164169099837440 |
---|---|
author | Favre, David Lederer, Sharon Kanwar, Bittoo Ma, Zhong-Min Proll, Sean Kasakow, Zeljka Mold, Jeff Swainson, Louise Barbour, Jason D. Baskin, Carole R. Palermo, Robert Pandrea, Ivona Miller, Christopher J. Katze, Michael G. McCune, Joseph M. |
author_facet | Favre, David Lederer, Sharon Kanwar, Bittoo Ma, Zhong-Min Proll, Sean Kasakow, Zeljka Mold, Jeff Swainson, Louise Barbour, Jason D. Baskin, Carole R. Palermo, Robert Pandrea, Ivona Miller, Christopher J. Katze, Michael G. McCune, Joseph M. |
author_sort | Favre, David |
collection | PubMed |
description | Chronic immune activation and progression to AIDS are observed after SIV infection in macaques but not in natural host primate species. To better understand this dichotomy, we compared acute pathogenic SIV infection in pigtailed macaques (PTs) to non-pathogenic infection in African green monkeys (AGMs). SIVagm-infected PTs, but not SIVagm-infected AGMs, rapidly developed systemic immune activation, marked and selective depletion of IL-17-secreting (Th17) cells, and loss of the balance between Th17 and T regulatory (Treg) cells in blood, lymphoid organs, and mucosal tissue. The loss of Th17 cells was found to be predictive of systemic and sustained T cell activation. Collectively, these data indicate that loss of the Th17 to Treg balance is related to SIV disease progression. |
format | Text |
id | pubmed-2635016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26350162009-02-13 Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection Favre, David Lederer, Sharon Kanwar, Bittoo Ma, Zhong-Min Proll, Sean Kasakow, Zeljka Mold, Jeff Swainson, Louise Barbour, Jason D. Baskin, Carole R. Palermo, Robert Pandrea, Ivona Miller, Christopher J. Katze, Michael G. McCune, Joseph M. PLoS Pathog Research Article Chronic immune activation and progression to AIDS are observed after SIV infection in macaques but not in natural host primate species. To better understand this dichotomy, we compared acute pathogenic SIV infection in pigtailed macaques (PTs) to non-pathogenic infection in African green monkeys (AGMs). SIVagm-infected PTs, but not SIVagm-infected AGMs, rapidly developed systemic immune activation, marked and selective depletion of IL-17-secreting (Th17) cells, and loss of the balance between Th17 and T regulatory (Treg) cells in blood, lymphoid organs, and mucosal tissue. The loss of Th17 cells was found to be predictive of systemic and sustained T cell activation. Collectively, these data indicate that loss of the Th17 to Treg balance is related to SIV disease progression. Public Library of Science 2009-02-13 /pmc/articles/PMC2635016/ /pubmed/19214220 http://dx.doi.org/10.1371/journal.ppat.1000295 Text en Favre et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Favre, David Lederer, Sharon Kanwar, Bittoo Ma, Zhong-Min Proll, Sean Kasakow, Zeljka Mold, Jeff Swainson, Louise Barbour, Jason D. Baskin, Carole R. Palermo, Robert Pandrea, Ivona Miller, Christopher J. Katze, Michael G. McCune, Joseph M. Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title | Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title_full | Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title_fullStr | Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title_full_unstemmed | Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title_short | Critical Loss of the Balance between Th17 and T Regulatory Cell Populations in Pathogenic SIV Infection |
title_sort | critical loss of the balance between th17 and t regulatory cell populations in pathogenic siv infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635016/ https://www.ncbi.nlm.nih.gov/pubmed/19214220 http://dx.doi.org/10.1371/journal.ppat.1000295 |
work_keys_str_mv | AT favredavid criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT lederersharon criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT kanwarbittoo criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT mazhongmin criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT prollsean criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT kasakowzeljka criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT moldjeff criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT swainsonlouise criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT barbourjasond criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT baskincaroler criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT palermorobert criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT pandreaivona criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT millerchristopherj criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT katzemichaelg criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection AT mccunejosephm criticallossofthebalancebetweenth17andtregulatorycellpopulationsinpathogenicsivinfection |