Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/39498
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dc.contributor.authorMcDonald C.A.en
dc.contributor.authorAllison B.J.en
dc.contributor.authorFahey M.C.en
dc.contributor.authorJenkin G.en
dc.contributor.authorMiller S.L.en
dc.contributor.authorPaton M.C.B.en
dc.date.accessioned2021-05-14T13:28:57Zen
dc.date.available2021-05-14T13:28:57Zen
dc.date.copyright2017en
dc.date.created20170518en
dc.date.issued2017-05-18en
dc.identifier.citationFrontiers in Neuroscience. 11 (APR) (no pagination), 2017. Article Number: 200. Date of Publication: 10 Apr 2017.en
dc.identifier.issn1662-4548en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/39498en
dc.description.abstractChorioamnionitis is a major cause of preterm birth and brain injury. Bacterial invasion of the chorion and amnion, and/or the placenta, can lead to a fetal inflammatory response, which in turn has significant adverse consequences for the developing fetal brain. Accordingly, there is a strong causal link between chorioamnionitis, preterm brain injury and the pathogenesis of severe postnatal neurological deficits and cerebral palsy. Currently there are no treatments to protect or repair against brain injury in preterm infants born after pregnancy compromised by intrauterine infection. This review describes the injurious cascade of events in the preterm brain in response to a severe fetal inflammatory event. We will highlight specific periods of increased vulnerability, and the potential effects of therapeutic intervention with cell-based therapies. Many clinical trials are underway to investigate the efficacy of stem cells to treat patients with cerebral palsy. Stem cells, obtained from umbilical cord tissue and cord blood, normally discarded after birth, are emerging as a safe and potentially effective therapy. It is not yet known, however, which stem cell type(s) are the most efficacious for administration to preterm infants to treat brain injury-mediated inflammation. Individual stem cell populations found in cord blood and tissue, such as mesenchymal stem cells (MSCs) and endothelial progenitor cells (EPCs), have a number of potential benefits that may specifically target preterm inflammatory-induced brain injury. MSCs have strong immunomodulatory potential, protecting against global and local neuroinflammatory cascades triggered during infection to the fetus. EPCs have angiogenic and vascular reparative qualities that make them ideal for neurovascular repair. A combined therapy using both MSCs and EPCs to target inflammation and promote angiogenesis for re-establishment of vital vessel networks is a treatment concept that warrants further investigation.Copyright © 2017 Paton, McDonald, Allison, Fahey, Jenkin and Miller.en
dc.languageEnglishen
dc.languageenen
dc.publisherFrontiers Research Foundation (E-mail: info@frontiersin.org)en
dc.relation.ispartofFrontiers in Neuroscienceen
dc.titlePerinatal brain injury as a consequence of preterm birth and intrauterine inflammation: Designing targeted stem cell therapies.en
dc.typeReviewen
dc.type.studyortrialReview article (e.g. literature review, narrative review)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3389/fnins.2017.00200en
dc.publisher.placeSwitzerlanden
dc.identifier.source615986509en
dc.identifier.institution(Paton, McDonald, Allison, Fahey, Jenkin, Miller) Neurodevelopment and Neuroprotection Research Group, The Ritchie Centre, Hudson Institute of Medical Research, Monash University, Clayton, VIC, Australia (Paton, Jenkin, Miller) Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, VIC, Australia (Fahey) Department of Paediatrics, Monash University, Clayton, VIC, Australiaen
dc.description.addressS.L. Miller, Neurodevelopment and Neuroprotection Research Group, The Ritchie Centre, Hudson Institute of Medical Research, Monash University, Clayton, VIC, Australia. E-mail: suzie.miller@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2017 Elsevier B.V., All rights reserved.en
dc.subect.keywordsBrain Chorioamnionitis Endothelial progenitor cells Inflammation Mesenchymal stem cells, cerebral palsy Preterm Stem cellsen
dc.identifier.authoremailMiller S.L.; suzie.miller@monash.eduen
dc.description.grantOrganization: (NHMRC) *National Health and Medical Research Council*en
dc.identifier.affiliationext(Paton, McDonald, Allison, Fahey, Jenkin, Miller) Neurodevelopment and Neuroprotection Research Group, The Ritchie Centre, Hudson Institute of Medical Research, Monash University, Clayton, VIC, Australia-
dc.identifier.affiliationext(Fahey) Department of Paediatrics, Monash University, Clayton, VIC, Australia-
dc.identifier.affiliationmh(Paton, Jenkin, Miller) Department of Obstetrics and Gynaecology, Monash Medical Centre, Monash University, Clayton, VIC, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeReview-
crisitem.author.deptObstetrics and Gynaecology (Monash Women's)-
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