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dc.contributor.advisorFletcher, Jean
dc.contributor.authorBasdeo, Sharee Ann
dc.date.accessioned2017-02-23T14:55:53Z
dc.date.available2017-02-23T14:55:53Z
dc.date.issued2015
dc.identifier.citationSharee Ann Basdeo, 'The pathogenicity and regulation of CD161⁺Th17 lineage cells in rheumatoid arthritis', [thesis], Trinity College (Dublin, Ireland). School of Biochemistry and Immunology, 2015, pp 271
dc.identifier.otherTHESIS 10523
dc.description.abstractPathogenic Th17 cells, which produce their signature cytokine IL-17, play a key role in autoimmune diseases such as rheumatoid arthritis (RA) and therefore, have been the target of recently developed therapeutics. On the other hand, Treg cells act to constrain effector T cell responses and play an important role in maintaining tolerance. The aim of this study was to investigate the regulation of Th17 cells by Treg cells in the context of the RA joint. In recent years it has emerged that both Treg and Th17 cells exhibit significant functional plasticity, particularly under conditions of inflammation.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Biochemistry and Immunology
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb16100695
dc.subjectImmunology, Ph.D.
dc.subjectPh.D. Trinity College Dublin
dc.titleThe pathogenicity and regulation of CD161⁺Th17 lineage cells in rheumatoid arthritis
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 271
dc.description.noteTARA (Trinity’s Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie
dc.identifier.urihttp://hdl.handle.net/2262/79481


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