Peripheral immune cells and perinatal brain injury: a double-edged sword?
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Published on: February 16, 2018
Josephine Herz1,2, Ivo Bendix3,4, Ursula Felderhoff-Müser5,6
1Department of Paediatrics I, Neonatology and Experimental Perinatal Neurosciences, University Hospital Essen, University Duisburg-Essen, Essen, Germany. Josephine.herz@uk-essen.de.
Insights
Perinatal brain injury involves complex neuroinflammation. This review details how immune cells contribute to damage and repair in conditions like prematurity and neonatal encephalopathy, guiding new therapies.
Area of Science:
- Neuroscience
- Immunology
- Developmental Biology
Background:
- Perinatal brain injury is a major cause of childhood neurological disability.
- Noxious stimuli like inflammation, hypoxia, and drug exposure contribute to its pathogenesis.
- The developing immune system critically influences immature brain injury mechanisms.
Purpose of the Study:
- To review the role of peripheral immune cells in perinatal brain injury.
- To discuss neuroinflammation in encephalopathy of prematurity (EoP) and neonatal encephalopathy (NE).
- To explore sex differences, maturational stages, and therapeutic targets.
Main Methods:
- Review of current literature on immune cell subsets in perinatal brain injury.
- Analysis of immune cell infiltration routes and functions.
- Discussion of interactions with regenerative therapies and immunomodulatory targets.
Main Results:
- Peripheral immune cells significantly contribute to both brain damage and repair post-insult.
- Specific immune cell subsets and their infiltration pathways are crucial in EoP and NE.
- Maturation stage and sex influence the neuroinflammatory response and injury outcomes.
Conclusions:
- Understanding immune cell roles is vital for developing targeted immunomodulatory therapies.
- Novel therapeutic strategies may leverage immune responses for brain repair.
- Further research into sex-specific and maturation-dependent immune mechanisms is warranted.
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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