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Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?

BACKGROUND: The influenza vaccine has shown promise as a mild, exogenous inflammatory challenge, but use of this model is limited by lack of knowledge about the timing of the inflammatory response. This study was designed to characterize the time-course of the acute inflammatory response and explore...

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Autores principales: Radin, Arielle S., Kuhlman, Kate R., Boyle, Chloe C., Haydon, Marcie D., Bower, Julienne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474380/
https://www.ncbi.nlm.nih.gov/pubmed/34589752
http://dx.doi.org/10.1016/j.bbih.2021.100239
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author Radin, Arielle S.
Kuhlman, Kate R.
Boyle, Chloe C.
Haydon, Marcie D.
Bower, Julienne E.
author_facet Radin, Arielle S.
Kuhlman, Kate R.
Boyle, Chloe C.
Haydon, Marcie D.
Bower, Julienne E.
author_sort Radin, Arielle S.
collection PubMed
description BACKGROUND: The influenza vaccine has shown promise as a mild, exogenous inflammatory challenge, but use of this model is limited by lack of knowledge about the timing of the inflammatory response. This study was designed to characterize the time-course of the acute inflammatory response and explore psychological and behavioral predictors of that response. METHODS: Twenty-one young, healthy individuals were recruited to receive the annual influenza vaccine. Serial blood samples were collected immediately before, and 24, 48, and 72 ​h following influenza vaccination. Interleukin (IL)-6 concentrations were assayed at each time-point and psychological and behavioral factors (anxiety and depressive symptoms, sleep disturbance, and childhood adversity) were assessed at baseline. RESULTS: Significant elevations in IL-6 were observed at 24 ​h post-vaccination (mean increase ​= ​0.70 ​pg/mL, Cohen’s d ​= ​0.54, p ​= ​.018)), with 61.9% of participants exhibiting peak concentrations at that time point, χ(2) ​= ​22.54, p ​< ​.001, η ​= ​0.52. In exploratory analyses, sleep disturbance was associated with greater increases in IL-6 at 24 ​h. CONCLUSIONS: By identifying the peak IL-6 response to influenza vaccination among a sample of young, healthy individuals, these findings support the use of the influenza vaccine in future PNI research. This vaccine model can be used to examine the impact of mild inflammatory challenges on the brain and behavior, and to identify psychological and behavioral factors (e.g., anxiety, sleep) that modulate inflammatory reactivity.
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spelling pubmed-84743802021-09-28 Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak? Radin, Arielle S. Kuhlman, Kate R. Boyle, Chloe C. Haydon, Marcie D. Bower, Julienne E. Brain Behav Immun Health Short Communication BACKGROUND: The influenza vaccine has shown promise as a mild, exogenous inflammatory challenge, but use of this model is limited by lack of knowledge about the timing of the inflammatory response. This study was designed to characterize the time-course of the acute inflammatory response and explore psychological and behavioral predictors of that response. METHODS: Twenty-one young, healthy individuals were recruited to receive the annual influenza vaccine. Serial blood samples were collected immediately before, and 24, 48, and 72 ​h following influenza vaccination. Interleukin (IL)-6 concentrations were assayed at each time-point and psychological and behavioral factors (anxiety and depressive symptoms, sleep disturbance, and childhood adversity) were assessed at baseline. RESULTS: Significant elevations in IL-6 were observed at 24 ​h post-vaccination (mean increase ​= ​0.70 ​pg/mL, Cohen’s d ​= ​0.54, p ​= ​.018)), with 61.9% of participants exhibiting peak concentrations at that time point, χ(2) ​= ​22.54, p ​< ​.001, η ​= ​0.52. In exploratory analyses, sleep disturbance was associated with greater increases in IL-6 at 24 ​h. CONCLUSIONS: By identifying the peak IL-6 response to influenza vaccination among a sample of young, healthy individuals, these findings support the use of the influenza vaccine in future PNI research. This vaccine model can be used to examine the impact of mild inflammatory challenges on the brain and behavior, and to identify psychological and behavioral factors (e.g., anxiety, sleep) that modulate inflammatory reactivity. Elsevier 2021-03-04 /pmc/articles/PMC8474380/ /pubmed/34589752 http://dx.doi.org/10.1016/j.bbih.2021.100239 Text en © 2021 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Radin, Arielle S.
Kuhlman, Kate R.
Boyle, Chloe C.
Haydon, Marcie D.
Bower, Julienne E.
Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title_full Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title_fullStr Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title_full_unstemmed Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title_short Using the influenza vaccine as a mild, exogenous inflammatory challenge: When does inflammation peak?
title_sort using the influenza vaccine as a mild, exogenous inflammatory challenge: when does inflammation peak?
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474380/
https://www.ncbi.nlm.nih.gov/pubmed/34589752
http://dx.doi.org/10.1016/j.bbih.2021.100239
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