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dc.contributor.authorKurne, Asli
dc.contributor.authorSayat, Guliz
dc.contributor.authorAydin, Omer Faruk
dc.contributor.authorTurgutoglu, Nihan
dc.contributor.authorTerzi, Murat
dc.contributor.authorSackesen, Cansin
dc.contributor.authorKarabudak, Rana
dc.date.accessioned2020-06-21T14:17:52Z
dc.date.available2020-06-21T14:17:52Z
dc.date.issued2012
dc.identifier.issn0165-5728
dc.identifier.urihttps://doi.org/10.1016/j.jneuroim.2012.05.005
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16346
dc.descriptionWOS: 000308899300012en_US
dc.descriptionPubMed: 22703766en_US
dc.description.abstractSoluble (s) CD14, being a receptor for lipopolysaccharides (LPSs) may inhibit LPS-triggered apoptosis and T lymphocyte proliferation. C to T exchange at position - 159 in the promoter region of the CD14 gene might lead to higher sCD14 levels. Limited number of groups have studied whether these polymorphisms might influence the development of organ specific autoimmunity and whether higher CD14 levels are associated with increased levels of cytokines trigerring inflammatory processes. However their data contradict each other. In this study serum levels of sCD14 based on ELISA were measured in 77 treatment-naive patients and in 67 healthy controls. As the C - 159T proximal promoter region regulates 5CD14 levels, we investigated whether C - 159T polymorphism is related to progression index in 250 MS patients vs. 183 healthy controls. CD14 polymorphism frequency between the healthy controls and the MS patients were not significantly different. While TT genotype of MS patients demonstrated significantly lower 5CD14 levels compared to CC genotype: this difference was not reflected on the disease progression index. Our study that extends the prior data of previous studies reflects that 5CD14 do not appear to be a solely prominent element of innate immunity in MS. (c) 2012 Published by Elsevier B.V.en_US
dc.language.isoengen_US
dc.publisherElsevier Science Bven_US
dc.relation.isversionof10.1016/j.jneuroim.2012.05.005en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMultiple sclerosisen_US
dc.subjectRRMSen_US
dc.subjectSoluble CD14en_US
dc.subjectCD14 polymorphismen_US
dc.subjectProgression indexen_US
dc.titleLack of association of the CD14/C-159T polymorphism with susceptibility and progression parameters in Turkish multiple sclerosis patientsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume250en_US
dc.identifier.issue01.Feben_US
dc.identifier.startpage83en_US
dc.identifier.endpage86en_US
dc.relation.journalJournal of Neuroimmunologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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