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Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants

BACKGROUND: A prerequisite for an effective innate immunity is the migrative ability of neutrophils to respond to inflammatory and infectious agents such as the intermediate interleukin (IL)-8 and the end-target formyl-methionyl-leucyl-phenylalanine (fMLP) chemoattractants. The aim was to study the...

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Autores principales: Stålhammar, Maria E., Douhan Håkansson, Lena, Jonzon, Anders, Sindelar, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361430/
https://www.ncbi.nlm.nih.gov/pubmed/27690722
http://dx.doi.org/10.1080/03009734.2016.1228721
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author Stålhammar, Maria E.
Douhan Håkansson, Lena
Jonzon, Anders
Sindelar, Richard
author_facet Stålhammar, Maria E.
Douhan Håkansson, Lena
Jonzon, Anders
Sindelar, Richard
author_sort Stålhammar, Maria E.
collection PubMed
description BACKGROUND: A prerequisite for an effective innate immunity is the migrative ability of neutrophils to respond to inflammatory and infectious agents such as the intermediate interleukin (IL)-8 and the end-target formyl-methionyl-leucyl-phenylalanine (fMLP) chemoattractants. The aim was to study the chemotactic capacity of neutrophils from newborn infants and adults in response to IL-8 and the bacterial peptide fMLP. METHODS: In the under-agarose cell migration assay, isolated leukocytes from healthy adults and from cord blood of healthy term newborn infants were studied with dose responses towards IL-8 and fMLP. The same number of leukocytes (1 × 10(5) cells), with the same distribution of neutrophils and monocytes, were analyzed in neonates and adults. Chemotaxis was distinguished from randomly migrating neutrophils, and the neutrophil pattern of migration, i.e. the migration distance and the number of migrating neutrophils per distance, was evaluated. RESULTS: In comparison to adults, fewer neutrophils from newborn infants migrated towards IL-8 and for a shorter distance (P < .01, respectively). The number of neutrophils migrating to different gradients of fMLP, the distance they migrated, and the correlation between the number and the distance were the same for neonates and adults. Random migration did not differ in any instance. CONCLUSION: Chemotaxis of neutrophils from newborn infants was as co-ordinated as neutrophils from adults in response to fMLP, whereas the response to IL-8 was reduced. The differential response of neutrophils from neonates to intermediate and end-target chemoattractants could indicate a reduced infectious response.
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spelling pubmed-53614302017-03-29 Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants Stålhammar, Maria E. Douhan Håkansson, Lena Jonzon, Anders Sindelar, Richard Ups J Med Sci Original Articles BACKGROUND: A prerequisite for an effective innate immunity is the migrative ability of neutrophils to respond to inflammatory and infectious agents such as the intermediate interleukin (IL)-8 and the end-target formyl-methionyl-leucyl-phenylalanine (fMLP) chemoattractants. The aim was to study the chemotactic capacity of neutrophils from newborn infants and adults in response to IL-8 and the bacterial peptide fMLP. METHODS: In the under-agarose cell migration assay, isolated leukocytes from healthy adults and from cord blood of healthy term newborn infants were studied with dose responses towards IL-8 and fMLP. The same number of leukocytes (1 × 10(5) cells), with the same distribution of neutrophils and monocytes, were analyzed in neonates and adults. Chemotaxis was distinguished from randomly migrating neutrophils, and the neutrophil pattern of migration, i.e. the migration distance and the number of migrating neutrophils per distance, was evaluated. RESULTS: In comparison to adults, fewer neutrophils from newborn infants migrated towards IL-8 and for a shorter distance (P < .01, respectively). The number of neutrophils migrating to different gradients of fMLP, the distance they migrated, and the correlation between the number and the distance were the same for neonates and adults. Random migration did not differ in any instance. CONCLUSION: Chemotaxis of neutrophils from newborn infants was as co-ordinated as neutrophils from adults in response to fMLP, whereas the response to IL-8 was reduced. The differential response of neutrophils from neonates to intermediate and end-target chemoattractants could indicate a reduced infectious response. Taylor & Francis 2017-03 2016-10-03 /pmc/articles/PMC5361430/ /pubmed/27690722 http://dx.doi.org/10.1080/03009734.2016.1228721 Text en © 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 work is properly cited.
spellingShingle Original Articles
Stålhammar, Maria E.
Douhan Håkansson, Lena
Jonzon, Anders
Sindelar, Richard
Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title_full Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title_fullStr Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title_full_unstemmed Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title_short Differential neutrophil chemotactic response towards IL-8 and bacterial N-formyl peptides in term newborn infants
title_sort differential neutrophil chemotactic response towards il-8 and bacterial n-formyl peptides in term newborn infants
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5361430/
https://www.ncbi.nlm.nih.gov/pubmed/27690722
http://dx.doi.org/10.1080/03009734.2016.1228721
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