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Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis

The response of the adaptive immune system is usually less intense in premature neonates than term neonates. The primary objective of this study was to determine whether immunological parameters vary between preterm (PT) neonates (≥32 weeks of gestational age) and very preterm (VPT) neonates (<32...

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Autores principales: Segura-Cervantes, Enrique, Mancilla-Ramírez, Javier, González-Canudas, Jorge, Alba, Erika, Santillán-Ballesteros, René, Morales-Barquet, Deneb, Sandoval-Plata, Gabriela, Galindo-Sevilla, Norma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884838/
https://www.ncbi.nlm.nih.gov/pubmed/27293317
http://dx.doi.org/10.1155/2016/6740827
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author Segura-Cervantes, Enrique
Mancilla-Ramírez, Javier
González-Canudas, Jorge
Alba, Erika
Santillán-Ballesteros, René
Morales-Barquet, Deneb
Sandoval-Plata, Gabriela
Galindo-Sevilla, Norma
author_facet Segura-Cervantes, Enrique
Mancilla-Ramírez, Javier
González-Canudas, Jorge
Alba, Erika
Santillán-Ballesteros, René
Morales-Barquet, Deneb
Sandoval-Plata, Gabriela
Galindo-Sevilla, Norma
author_sort Segura-Cervantes, Enrique
collection PubMed
description The response of the adaptive immune system is usually less intense in premature neonates than term neonates. The primary objective of this study was to determine whether immunological parameters vary between preterm (PT) neonates (≥32 weeks of gestational age) and very preterm (VPT) neonates (<32 weeks of gestational age). A cross-sectional study was designed to prospectively follow PT and VPT neonates at risk of developing sepsis. Plasma concentrations of IFN-γ, TNF-α, IL-6, IL-4, and IL-10 were detected using flow cytometry. C-reactive protein (C-RP) and the complex SC5b-9 were detected in the plasma using commercial kits. A total of 83 patients were included. The laboratory results and clinical histories showed that 26 patients had sepsis; 14 were VPT, and 12 were PT. The levels of C-RP, SC5b-9 (innate immune response mediators), and IL-10 or IL-4 (anti-inflammatory cytokines) were elevated during sepsis in both groups. IFN-γ, TNF-α, and IL-6 (proinflammatory cytokines) were differentially elevated only in PT neonates. The VPT neonates with sepsis presented increases in C-RP, SC5b-9, and anti-inflammatory cytokines but not in proinflammatory cytokines, whereas PT neonates showed increases in all studied mediators of inflammation.
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spelling pubmed-48848382016-06-12 Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis Segura-Cervantes, Enrique Mancilla-Ramírez, Javier González-Canudas, Jorge Alba, Erika Santillán-Ballesteros, René Morales-Barquet, Deneb Sandoval-Plata, Gabriela Galindo-Sevilla, Norma Mediators Inflamm Research Article The response of the adaptive immune system is usually less intense in premature neonates than term neonates. The primary objective of this study was to determine whether immunological parameters vary between preterm (PT) neonates (≥32 weeks of gestational age) and very preterm (VPT) neonates (<32 weeks of gestational age). A cross-sectional study was designed to prospectively follow PT and VPT neonates at risk of developing sepsis. Plasma concentrations of IFN-γ, TNF-α, IL-6, IL-4, and IL-10 were detected using flow cytometry. C-reactive protein (C-RP) and the complex SC5b-9 were detected in the plasma using commercial kits. A total of 83 patients were included. The laboratory results and clinical histories showed that 26 patients had sepsis; 14 were VPT, and 12 were PT. The levels of C-RP, SC5b-9 (innate immune response mediators), and IL-10 or IL-4 (anti-inflammatory cytokines) were elevated during sepsis in both groups. IFN-γ, TNF-α, and IL-6 (proinflammatory cytokines) were differentially elevated only in PT neonates. The VPT neonates with sepsis presented increases in C-RP, SC5b-9, and anti-inflammatory cytokines but not in proinflammatory cytokines, whereas PT neonates showed increases in all studied mediators of inflammation. Hindawi Publishing Corporation 2016 2016-05-16 /pmc/articles/PMC4884838/ /pubmed/27293317 http://dx.doi.org/10.1155/2016/6740827 Text en Copyright © 2016 Enrique Segura-Cervantes et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Segura-Cervantes, Enrique
Mancilla-Ramírez, Javier
González-Canudas, Jorge
Alba, Erika
Santillán-Ballesteros, René
Morales-Barquet, Deneb
Sandoval-Plata, Gabriela
Galindo-Sevilla, Norma
Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title_full Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title_fullStr Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title_full_unstemmed Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title_short Inflammatory Response in Preterm and Very Preterm Newborns with Sepsis
title_sort inflammatory response in preterm and very preterm newborns with sepsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884838/
https://www.ncbi.nlm.nih.gov/pubmed/27293317
http://dx.doi.org/10.1155/2016/6740827
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