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PTSD, a Disorder with an Immunological Component

Post-traumatic stress disorder (PTSD) has been associated with an inflammatory state. However, few studies have addressed the mechanisms underlying this immune imbalance that favors inflammation or how this imbalance contributes to PTSD. Whether the immune imbalance influences responsiveness or unre...

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Detalles Bibliográficos
Autores principales: Wang, Zhewu, Young, M. Rita I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893499/
https://www.ncbi.nlm.nih.gov/pubmed/27375619
http://dx.doi.org/10.3389/fimmu.2016.00219
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author Wang, Zhewu
Young, M. Rita I.
author_facet Wang, Zhewu
Young, M. Rita I.
author_sort Wang, Zhewu
collection PubMed
description Post-traumatic stress disorder (PTSD) has been associated with an inflammatory state. However, few studies have addressed the mechanisms underlying this immune imbalance that favors inflammation or how this imbalance contributes to PTSD. Whether the immune imbalance influences responsiveness or unresponsiveness of patients to PTSD treatments is currently not known. This review brings forward an immune emphasis to a mental health disorder that is unprecedented in its prevalence among combat Veterans of the ongoing conflicts in Iraq and Afghanistan and which also afflicts civilians who have undergone extreme traumatic experiences, such as following natural disasters, serious accidents, or assaults. Included is an overview of the correlative associations in human subjects between PTSD and inflammation and studies in animal models of PTSD, demonstrating causal contributions of inflammation and immune dysregulation to PTSD-like behavior following stress exposure.
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spelling pubmed-48934992016-07-01 PTSD, a Disorder with an Immunological Component Wang, Zhewu Young, M. Rita I. Front Immunol Immunology Post-traumatic stress disorder (PTSD) has been associated with an inflammatory state. However, few studies have addressed the mechanisms underlying this immune imbalance that favors inflammation or how this imbalance contributes to PTSD. Whether the immune imbalance influences responsiveness or unresponsiveness of patients to PTSD treatments is currently not known. This review brings forward an immune emphasis to a mental health disorder that is unprecedented in its prevalence among combat Veterans of the ongoing conflicts in Iraq and Afghanistan and which also afflicts civilians who have undergone extreme traumatic experiences, such as following natural disasters, serious accidents, or assaults. Included is an overview of the correlative associations in human subjects between PTSD and inflammation and studies in animal models of PTSD, demonstrating causal contributions of inflammation and immune dysregulation to PTSD-like behavior following stress exposure. Frontiers Media S.A. 2016-06-06 /pmc/articles/PMC4893499/ /pubmed/27375619 http://dx.doi.org/10.3389/fimmu.2016.00219 Text en Copyright © 2016 Wang and Young. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wang, Zhewu
Young, M. Rita I.
PTSD, a Disorder with an Immunological Component
title PTSD, a Disorder with an Immunological Component
title_full PTSD, a Disorder with an Immunological Component
title_fullStr PTSD, a Disorder with an Immunological Component
title_full_unstemmed PTSD, a Disorder with an Immunological Component
title_short PTSD, a Disorder with an Immunological Component
title_sort ptsd, a disorder with an immunological component
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893499/
https://www.ncbi.nlm.nih.gov/pubmed/27375619
http://dx.doi.org/10.3389/fimmu.2016.00219
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