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Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients

BACKGROUND: To investigate natural killer (NK) cell activity, circulating cytokine level and peripheral blood mononuclear cell (PBMC) cytokine production status in critically ill patients. METHODS: Blood samples were collected <24 h after admission from 24 intensive care unit (ICU) patients and 2...

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Autores principales: Kim, Minkyung, Kim, Minjoo, Jeong, Hana, Chae, Jey Sook, Kim, Young Sam, Lee, Jae Gil, Cho, Younsoo, Lee, Jong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723033/
https://www.ncbi.nlm.nih.gov/pubmed/29221433
http://dx.doi.org/10.1186/s12865-017-0231-y
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author Kim, Minkyung
Kim, Minjoo
Jeong, Hana
Chae, Jey Sook
Kim, Young Sam
Lee, Jae Gil
Cho, Younsoo
Lee, Jong Ho
author_facet Kim, Minkyung
Kim, Minjoo
Jeong, Hana
Chae, Jey Sook
Kim, Young Sam
Lee, Jae Gil
Cho, Younsoo
Lee, Jong Ho
author_sort Kim, Minkyung
collection PubMed
description BACKGROUND: To investigate natural killer (NK) cell activity, circulating cytokine level and peripheral blood mononuclear cell (PBMC) cytokine production status in critically ill patients. METHODS: Blood samples were collected <24 h after admission from 24 intensive care unit (ICU) patients and 24 age-, sex-, and body mass index (BMI)-matched healthy controls. Serum cytokine concentrations and cytokine production by PBMCs and lipopolysaccharide (LPS)-stimulated PBMCs were measured. RESULTS: The ICU group showed lower NK cell activity than the controls under all conditions and an absence of interferon (IFN)-γ. After adjusting for triglycerides, LDL- and HDL-cholesterol, and glucose, the ICU group exhibited lower serum levels of albumin and interleukin (IL)-12 and higher leukocyte counts and hs-CRP and IL-6 levels than the controls. Non-stimulated PBMCs from ICU patients secreted significantly greater amounts of IL-6 and IL-1β than the controls; however, the production of IL-6, TNF-α and IL-1β in response to LPS stimulation was significantly lower in the ICU group. CONCLUSIONS: Significant reductions in NK cell activity and serum IL-12 level, an absence of serum IFN-γ, and decreased cytokine production from LPS-stimulated PBMCs indicate the hyporesponsiveness of NK cells and an impaired early phase inflammatory response in critically ill patients (ClinicalTrials.gov NCT02565589:). Retrospectively registered; October 1, 2015.
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spelling pubmed-57230332017-12-12 Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients Kim, Minkyung Kim, Minjoo Jeong, Hana Chae, Jey Sook Kim, Young Sam Lee, Jae Gil Cho, Younsoo Lee, Jong Ho BMC Immunol Research Article BACKGROUND: To investigate natural killer (NK) cell activity, circulating cytokine level and peripheral blood mononuclear cell (PBMC) cytokine production status in critically ill patients. METHODS: Blood samples were collected <24 h after admission from 24 intensive care unit (ICU) patients and 24 age-, sex-, and body mass index (BMI)-matched healthy controls. Serum cytokine concentrations and cytokine production by PBMCs and lipopolysaccharide (LPS)-stimulated PBMCs were measured. RESULTS: The ICU group showed lower NK cell activity than the controls under all conditions and an absence of interferon (IFN)-γ. After adjusting for triglycerides, LDL- and HDL-cholesterol, and glucose, the ICU group exhibited lower serum levels of albumin and interleukin (IL)-12 and higher leukocyte counts and hs-CRP and IL-6 levels than the controls. Non-stimulated PBMCs from ICU patients secreted significantly greater amounts of IL-6 and IL-1β than the controls; however, the production of IL-6, TNF-α and IL-1β in response to LPS stimulation was significantly lower in the ICU group. CONCLUSIONS: Significant reductions in NK cell activity and serum IL-12 level, an absence of serum IFN-γ, and decreased cytokine production from LPS-stimulated PBMCs indicate the hyporesponsiveness of NK cells and an impaired early phase inflammatory response in critically ill patients (ClinicalTrials.gov NCT02565589:). Retrospectively registered; October 1, 2015. BioMed Central 2017-12-08 /pmc/articles/PMC5723033/ /pubmed/29221433 http://dx.doi.org/10.1186/s12865-017-0231-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kim, Minkyung
Kim, Minjoo
Jeong, Hana
Chae, Jey Sook
Kim, Young Sam
Lee, Jae Gil
Cho, Younsoo
Lee, Jong Ho
Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title_full Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title_fullStr Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title_full_unstemmed Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title_short Hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
title_sort hyporesponsiveness of natural killer cells and impaired inflammatory responses in critically ill patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5723033/
https://www.ncbi.nlm.nih.gov/pubmed/29221433
http://dx.doi.org/10.1186/s12865-017-0231-y
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