Publication:
Interleukin-2 gene polymorphism in Turkish patients with Behcet's disease and its association with ocular involvement

dc.contributor.authorÖzçimen, Ahmet Ata
dc.contributor.buuauthorYücel, Ali
dc.contributor.buuauthorDilek, Kamil
dc.contributor.buuauthorSaba, Davit
dc.contributor.buuauthorYurtkuran, Mustafa Abbas
dc.contributor.buuauthorOral, Haluk Barbaros
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentNefroloji ve Romatoloji Ana Bilim Dalı
dc.contributor.departmentGöz Hastalıkları Ana Bilim Dalı
dc.contributor.departmentKalp Damar Cerrahisi Ana Bilim Dalı
dc.contributor.departmentİmmünoloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-0463-6818
dc.contributor.researcheridK-7285-2012
dc.contributor.scopusid57225839918
dc.contributor.scopusid56005080200
dc.contributor.scopusid55987378200
dc.contributor.scopusid7003389525
dc.contributor.scopusid7004498001
dc.date.accessioned2022-10-20T05:48:53Z
dc.date.available2022-10-20T05:48:53Z
dc.date.issued2013-10
dc.description.abstractBehcet's disease (BD) is a chronic immune-mediated systemic disease, characterized by oral and genital lesions and ocular inflammation. Several cytokine genes may play crucial roles in host susceptibility to BD, because the cytokine production capacity varies among individuals and depends on the cytokine gene polymorphisms. The association of the interleukin (IL)-2 gene polymorphisms with the susceptibility to BD was investigated in this study. DNA samples were obtained from a Turkish population of 97 patients with BD and 76 healthy control subjects. Polymorphisms of IL-2 gene at position -330 and +166 were determined using the polymerase chain reaction with sequence-specific primers. In the patients with BD, there was a significantly increased frequency of IL-2 -330 GT genotype. Interestingly, we demonstrated that the frequencies of IL-2 -330 GT and IL-2+166 GG genotypes were increased in BD patients with ocular involvement, whilst IL-2 -330 TT genotype was significantly decreased. Also, analysis of allele frequency demonstrated that the presence of G allele at position +166 of IL-2 seems to be a risk factor for ocular involvement. These results reveal that IL-2 -330 GT genotype may be a susceptibility factor for BD, whereas IL-2 -330 TT genotype seems to display a protective association with BD. Additionally, IL-2 gene polymorphisms might be associated with ocular involvement in BD.
dc.identifier.citationYücel, A. vd. (2013). "Interleukin-2 gene polymorphism in Turkish patients with Behcet's disease and its association with ocular involvement". International Journal of Immunogenetics, 40(5), 349-355.
dc.identifier.endpage355
dc.identifier.issn1744-3121
dc.identifier.issue5
dc.identifier.pubmed23331481
dc.identifier.scopus2-s2.0-84883650660
dc.identifier.startpage349
dc.identifier.urihttps://doi.org/10.1111/iji.12039
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1111/iji.12039
dc.identifier.urihttp://hdl.handle.net/11452/29153
dc.identifier.volume40
dc.identifier.wos000324023400001
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.bapT-2004/59
dc.relation.collaborationYurt içi
dc.relation.journalInternational Journal of Immunogenetics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGenetics & heredity
dc.subjectImmunology
dc.subjectSystemic-lupus-erythematosus
dc.subjectHan chinese population
dc.subjectMultiple-sclerosis
dc.subjectIl-2 gene
dc.subjectT-cells
dc.subjectOnline databases
dc.subjectFactor-V
dc.subjectInfection
dc.subjectCytokines
dc.subjectTurkey
dc.subject.emtreeGenomic DNA
dc.subject.emtreeInterleukin 2
dc.subject.emtreeAllele
dc.subject.emtreeArticle
dc.subject.emtreeBehcet disease
dc.subject.emtreeClinical feature
dc.subject.emtreeControlled study
dc.subject.emtreeCytokine production
dc.subject.emtreeDNA polymorphism
dc.subject.emtreeGene frequency
dc.subject.emtreeGene sequence
dc.subject.emtreeGenetic association
dc.subject.emtreeGenotype
dc.subject.emtreeHuman
dc.subject.emtreeMajor clinical study
dc.subject.emtreePolymerase chain reaction
dc.subject.emtreePriority journal
dc.subject.emtreeRisk factor
dc.subject.emtreeTurkey (republic)
dc.subject.meshBehcet syndrome
dc.subject.meshDNA
dc.subject.meshEye
dc.subject.meshFemale
dc.subject.meshGene frequency
dc.subject.meshGenetic predisposition to disease
dc.subject.meshGenotype
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshInterleukin-2
dc.subject.meshLymphocytes
dc.subject.meshMale
dc.subject.meshNeutrophils
dc.subject.meshPolymorphism, single nucleotide
dc.subject.meshTurkey
dc.subject.scopusFluorescence Lifetime; Esterases; Optical Imaging
dc.subject.wosGenetics & heredity
dc.subject.wosImmunology
dc.titleInterleukin-2 gene polymorphism in Turkish patients with Behcet's disease and its association with ocular involvement
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Göz Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Nefroloji ve Romatoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Kalp Damar Cerrahisi Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/İmmünoloji Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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