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Peripheral immune cells and perinatal brain injury: a double-edged sword?

ABSTRACT: Perinatal brain injury is the leading cause of neurological mortality and morbidity in childhood ranging from motor and cognitive impairment to behavioural and neuropsychiatric disorders. Various noxious stimuli, including perinatal inflammation, chronic and acute hypoxia, hyperoxia, stres...

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Autores principales: Herz, Josephine, Bendix, Ivo, Felderhoff-Müser, Ursula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816729/
https://www.ncbi.nlm.nih.gov/pubmed/34750522
http://dx.doi.org/10.1038/s41390-021-01818-7
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author Herz, Josephine
Bendix, Ivo
Felderhoff-Müser, Ursula
author_facet Herz, Josephine
Bendix, Ivo
Felderhoff-Müser, Ursula
author_sort Herz, Josephine
collection PubMed
description ABSTRACT: Perinatal brain injury is the leading cause of neurological mortality and morbidity in childhood ranging from motor and cognitive impairment to behavioural and neuropsychiatric disorders. Various noxious stimuli, including perinatal inflammation, chronic and acute hypoxia, hyperoxia, stress and drug exposure contribute to the pathogenesis. Among a variety of pathological phenomena, the unique developing immune system plays an important role in the understanding of mechanisms of injury to the immature brain. Neuroinflammation following a perinatal insult largely contributes to evolution of damage to resident brain cells, but may also be beneficial for repair activities. The present review will focus on the role of peripheral immune cells and discuss processes involved in neuroinflammation under two frequent perinatal conditions, systemic infection/inflammation associated with encephalopathy of prematurity (EoP) and hypoxia/ischaemia in the context of neonatal encephalopathy (NE) and stroke at term. Different immune cell subsets in perinatal brain injury including their infiltration routes will be reviewed and critical aspects such as sex differences and maturational stage will be discussed. Interactions with existing regenerative therapies such as stem cells and also potentials to develop novel immunomodulatory targets are considered. IMPACT: Comprehensive summary of current knowledge on the role of different immune cell subsets in perinatal brain injury including discussion of critical aspects to be considered for development of immunomodulatory therapies.
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spelling pubmed-88167292022-02-16 Peripheral immune cells and perinatal brain injury: a double-edged sword? Herz, Josephine Bendix, Ivo Felderhoff-Müser, Ursula Pediatr Res Review Article ABSTRACT: Perinatal brain injury is the leading cause of neurological mortality and morbidity in childhood ranging from motor and cognitive impairment to behavioural and neuropsychiatric disorders. Various noxious stimuli, including perinatal inflammation, chronic and acute hypoxia, hyperoxia, stress and drug exposure contribute to the pathogenesis. Among a variety of pathological phenomena, the unique developing immune system plays an important role in the understanding of mechanisms of injury to the immature brain. Neuroinflammation following a perinatal insult largely contributes to evolution of damage to resident brain cells, but may also be beneficial for repair activities. The present review will focus on the role of peripheral immune cells and discuss processes involved in neuroinflammation under two frequent perinatal conditions, systemic infection/inflammation associated with encephalopathy of prematurity (EoP) and hypoxia/ischaemia in the context of neonatal encephalopathy (NE) and stroke at term. Different immune cell subsets in perinatal brain injury including their infiltration routes will be reviewed and critical aspects such as sex differences and maturational stage will be discussed. Interactions with existing regenerative therapies such as stem cells and also potentials to develop novel immunomodulatory targets are considered. IMPACT: Comprehensive summary of current knowledge on the role of different immune cell subsets in perinatal brain injury including discussion of critical aspects to be considered for development of immunomodulatory therapies. Nature Publishing Group US 2021-11-08 2022 /pmc/articles/PMC8816729/ /pubmed/34750522 http://dx.doi.org/10.1038/s41390-021-01818-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Herz, Josephine
Bendix, Ivo
Felderhoff-Müser, Ursula
Peripheral immune cells and perinatal brain injury: a double-edged sword?
title Peripheral immune cells and perinatal brain injury: a double-edged sword?
title_full Peripheral immune cells and perinatal brain injury: a double-edged sword?
title_fullStr Peripheral immune cells and perinatal brain injury: a double-edged sword?
title_full_unstemmed Peripheral immune cells and perinatal brain injury: a double-edged sword?
title_short Peripheral immune cells and perinatal brain injury: a double-edged sword?
title_sort peripheral immune cells and perinatal brain injury: a double-edged sword?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8816729/
https://www.ncbi.nlm.nih.gov/pubmed/34750522
http://dx.doi.org/10.1038/s41390-021-01818-7
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