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Leukocyte recruitment in preterm and term infants

Impaired cellular innate immune defense accounts for susceptibility to sepsis and its high morbidity and mortality in preterm infants. Leukocyte recruitment is an integral part of the cellular immune response and follows a well-defined cascade of events from rolling of leukocytes along the endotheli...

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Detalles Bibliográficos
Autores principales: Karenberg, Katinka, Hudalla, Hannes, Frommhold, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078115/
https://www.ncbi.nlm.nih.gov/pubmed/27778308
http://dx.doi.org/10.1186/s40348-016-0063-5
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author Karenberg, Katinka
Hudalla, Hannes
Frommhold, David
author_facet Karenberg, Katinka
Hudalla, Hannes
Frommhold, David
author_sort Karenberg, Katinka
collection PubMed
description Impaired cellular innate immune defense accounts for susceptibility to sepsis and its high morbidity and mortality in preterm infants. Leukocyte recruitment is an integral part of the cellular immune response and follows a well-defined cascade of events from rolling of leukocytes along the endothelium to firm adhesion and finally transmigration which is concerted by a variety of adhesion molecules. Recent analytical advances such as fetal intravital microscopy have granted new insights into ontogenetic regulation and maturation of fetal immune cell recruitment. Understanding the fetal innate immune system is essential for targeted prevention and therapy of premature infants with severe infections or disorders of the immune system. This review gives an overview of the basic principles of leukocyte recruitment, particularly neutrophil trafficking, and its development during early life and highlights technical limitations to our current knowledge.
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spelling pubmed-50781152016-11-07 Leukocyte recruitment in preterm and term infants Karenberg, Katinka Hudalla, Hannes Frommhold, David Mol Cell Pediatr Mini Review Impaired cellular innate immune defense accounts for susceptibility to sepsis and its high morbidity and mortality in preterm infants. Leukocyte recruitment is an integral part of the cellular immune response and follows a well-defined cascade of events from rolling of leukocytes along the endothelium to firm adhesion and finally transmigration which is concerted by a variety of adhesion molecules. Recent analytical advances such as fetal intravital microscopy have granted new insights into ontogenetic regulation and maturation of fetal immune cell recruitment. Understanding the fetal innate immune system is essential for targeted prevention and therapy of premature infants with severe infections or disorders of the immune system. This review gives an overview of the basic principles of leukocyte recruitment, particularly neutrophil trafficking, and its development during early life and highlights technical limitations to our current knowledge. Springer Berlin Heidelberg 2016-10-24 /pmc/articles/PMC5078115/ /pubmed/27778308 http://dx.doi.org/10.1186/s40348-016-0063-5 Text en © The Author(s). 2016 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.
spellingShingle Mini Review
Karenberg, Katinka
Hudalla, Hannes
Frommhold, David
Leukocyte recruitment in preterm and term infants
title Leukocyte recruitment in preterm and term infants
title_full Leukocyte recruitment in preterm and term infants
title_fullStr Leukocyte recruitment in preterm and term infants
title_full_unstemmed Leukocyte recruitment in preterm and term infants
title_short Leukocyte recruitment in preterm and term infants
title_sort leukocyte recruitment in preterm and term infants
topic Mini Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078115/
https://www.ncbi.nlm.nih.gov/pubmed/27778308
http://dx.doi.org/10.1186/s40348-016-0063-5
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