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dc.contributor.authorDoherty, Dereken
dc.date.accessioned2022-02-24T07:56:44Z
dc.date.available2022-02-24T07:56:44Z
dc.date.issued2020en
dc.date.submitted2020en
dc.identifier.citationHuggard D., Doherty D.G., Molloy E.J., Immune Dysregulation in Children With Down Syndrome, Frontiers in Pediatrics, 8, 2020en
dc.identifier.issn22962360en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/98165
dc.descriptionPUBLISHEDen
dc.description.abstractDown syndrome (DS) is the most common genetic syndrome associated with immune defects. The extent of immune dysregulation in DS is substantial, spanning the innate and adaptive systems and including anomalies in: T and B cells, monocytes, neutrophil chemotaxis, circulating cytokines, and suboptimal antibody responses which all contribute to an increased risk of infections, poorer clinical outcomes and chronic inflammation in this vulnerable cohort. Other aspects of innate immunity may also be abnormal and contribute to the increased morbidity and warrant further interrogation such as: gamma delta T cell function, the inflammasome, Toll-like receptors and their pathways. Pharmacotherapies such as pavilizumab, pneumococcal and influenza immunizations, as well as potential immunoprophylactic agents such as pidotimod, azithromycin and Broncho-Vaxom may help alleviate the infectious consequences. Children with DS need to be managed with a heightened sense of awareness and urgency in the setting of sepsis and signs of chronic inflammation need regular screening and appropriate follow up.en
dc.language.isoenen
dc.relation.ispartofseriesFrontiers in Pediatricsen
dc.relation.ispartofseries8en
dc.rightsYen
dc.subjectDown syndromeen
dc.subjectImmune dysregulationen
dc.subjectImmunodeficiencyen
dc.subjectReviewen
dc.subjectInnate immunityen
dc.titleImmune Dysregulation in Children With Down Syndromeen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/dohertdeen
dc.identifier.rssinternalid224281en
dc.identifier.doihttp://dx.doi.org/10.3389/fped.2020.00073en
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0002-4394-658Xen


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