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Plasma cytokine profiles in very preterm infants with late-onset sepsis

INTRODUCTION: Deficiencies in innate immune responses may contribute to the increased susceptibility to infection in preterm infants. In vivo cytokine profiles in response to sepsis in very preterm infants are not fully understood. AIMS: To characterise plasma pro- and anti-inflammatory cytokine con...

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Autores principales: Hibbert, Julie, Strunk, Tobias, Simmer, Karen, Richmond, Peter, Burgner, David, Currie, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224469/
https://www.ncbi.nlm.nih.gov/pubmed/32407417
http://dx.doi.org/10.1371/journal.pone.0232933
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author Hibbert, Julie
Strunk, Tobias
Simmer, Karen
Richmond, Peter
Burgner, David
Currie, Andrew
author_facet Hibbert, Julie
Strunk, Tobias
Simmer, Karen
Richmond, Peter
Burgner, David
Currie, Andrew
author_sort Hibbert, Julie
collection PubMed
description INTRODUCTION: Deficiencies in innate immune responses may contribute to the increased susceptibility to infection in preterm infants. In vivo cytokine profiles in response to sepsis in very preterm infants are not fully understood. AIMS: To characterise plasma pro- and anti-inflammatory cytokine concentrations and pre-defined ratios in very preterm infants with late-onset sepsis (LOS). METHODS: In this observational study, peripheral blood samples were collected at the time of evaluation for suspected LOS from 31 preterm infants (<30 weeks gestational age). Plasma cytokine concentrations were determined by 12-plex immunoassay. RESULTS: IL-10, IFN-γ, IL-12p70, IP-10, IL-6 and CCL2 were elevated in the majority infants with LOS (n = 12) compared to those without LOS (n = 19). There was no difference in TNF-α, IL-1β, IL-17AF, IL-8 and IL-15 concentrations between groups. IL-10/TNF-α ratios were increased, while CCL2/IL-10 and IL-12p70/IL-10 ratios were decreased in infants with LOS compared to those without. CONCLUSION: Very preterm infants have a marked innate inflammatory response at the time of LOS. The increase in IL-10/TNF-α ratio may indicate early immune hypo-responsiveness. Longitudinal studies with a larger number of participants are required to understand immune responses and clinical outcomes following LOS in preterm infants.
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spelling pubmed-72244692020-06-01 Plasma cytokine profiles in very preterm infants with late-onset sepsis Hibbert, Julie Strunk, Tobias Simmer, Karen Richmond, Peter Burgner, David Currie, Andrew PLoS One Research Article INTRODUCTION: Deficiencies in innate immune responses may contribute to the increased susceptibility to infection in preterm infants. In vivo cytokine profiles in response to sepsis in very preterm infants are not fully understood. AIMS: To characterise plasma pro- and anti-inflammatory cytokine concentrations and pre-defined ratios in very preterm infants with late-onset sepsis (LOS). METHODS: In this observational study, peripheral blood samples were collected at the time of evaluation for suspected LOS from 31 preterm infants (<30 weeks gestational age). Plasma cytokine concentrations were determined by 12-plex immunoassay. RESULTS: IL-10, IFN-γ, IL-12p70, IP-10, IL-6 and CCL2 were elevated in the majority infants with LOS (n = 12) compared to those without LOS (n = 19). There was no difference in TNF-α, IL-1β, IL-17AF, IL-8 and IL-15 concentrations between groups. IL-10/TNF-α ratios were increased, while CCL2/IL-10 and IL-12p70/IL-10 ratios were decreased in infants with LOS compared to those without. CONCLUSION: Very preterm infants have a marked innate inflammatory response at the time of LOS. The increase in IL-10/TNF-α ratio may indicate early immune hypo-responsiveness. Longitudinal studies with a larger number of participants are required to understand immune responses and clinical outcomes following LOS in preterm infants. Public Library of Science 2020-05-14 /pmc/articles/PMC7224469/ /pubmed/32407417 http://dx.doi.org/10.1371/journal.pone.0232933 Text en © 2020 Hibbert 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hibbert, Julie
Strunk, Tobias
Simmer, Karen
Richmond, Peter
Burgner, David
Currie, Andrew
Plasma cytokine profiles in very preterm infants with late-onset sepsis
title Plasma cytokine profiles in very preterm infants with late-onset sepsis
title_full Plasma cytokine profiles in very preterm infants with late-onset sepsis
title_fullStr Plasma cytokine profiles in very preterm infants with late-onset sepsis
title_full_unstemmed Plasma cytokine profiles in very preterm infants with late-onset sepsis
title_short Plasma cytokine profiles in very preterm infants with late-onset sepsis
title_sort plasma cytokine profiles in very preterm infants with late-onset sepsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224469/
https://www.ncbi.nlm.nih.gov/pubmed/32407417
http://dx.doi.org/10.1371/journal.pone.0232933
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