Publication:
Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome

dc.contributor.buuauthorTuran, Hakan
dc.contributor.buuauthorBaşkan, Emel Bülbül
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.buuauthorKarkucak, Mutlu
dc.contributor.buuauthorTunali, Şükran
dc.contributor.buuauthorSarıcaoğlu, Hayriye
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGenetik Tıp Ana Bilim Dalı
dc.contributor.scopusid16835681500
dc.contributor.scopusid43760921800
dc.contributor.scopusid6602802424
dc.contributor.scopusid35388323500
dc.contributor.scopusid7004191748
dc.contributor.scopusid6603722836
dc.date.accessioned2022-03-18T07:30:12Z
dc.date.available2022-03-18T07:30:12Z
dc.date.issued2011
dc.description.abstractBackground: "Toll like receptor" (TLR) 9 functions in stepping in of native immune system against different viral and bacterial pathogens and induction of adaptive immune response effectively. TLR 9 gene polymorphism makes host predisposed to microbial pathogens by affecting the functional capabilities of the receptor. Objective: We aimed to determine if TLR 9 gene polymorphism makes a predisposition to "erythema multiforme" (EM), "Stevens Johnson syndrome" (SJS) and "Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome" (SJS/TEN). Methods: Forty-two patients clinically and/or histopathologically diagnosed as EM, SJS, and SJS/TEN overlap syndrome and 50 healthy control subjects were enrolled in our study. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was applied for TLR 9 gene 1237 thymine/cytosine (T/C) polymorphism. Genotypes were determined according to bands occurring on agarose gel electrophoresis. Results: In patients group, the frequencies of IT and TC genotypes were 73.8 % and 26.2 % while CC genotype wasn't detected. In control group, the frequencies of TT, TC and CC genotypes were 74 %, 24 %, and 2 %. There wasn't a statistically significant difference for TT, TC and CC genotypes between patients and controls. The frequencies of T and C alleles were 84.5 % and 15.5 % in patients and 86 % and 14 % in controls, respectively. Conclusion: Our results showed that there isn't any association between TLR gene polymorphism and EM, SJS, SJS/TEN overlap syndrome (Tab. 1, Fig. 1, Ref. 30).
dc.identifier.citationTuran, H. vd.(2011). "Toll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome". Bratislava Medical Journal-Bratislavske Lekarske Listy, 112(5), 260-263.
dc.identifier.endpage263
dc.identifier.issn0006-9248
dc.identifier.issue5
dc.identifier.pubmed21682079
dc.identifier.scopus2-s2.0-79957924998
dc.identifier.startpage260
dc.identifier.urihttp://hdl.handle.net/11452/25172
dc.identifier.volume112
dc.identifier.wos000290424100006
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherComenius Univ
dc.relation.journalBratislava Medical Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGeneral & internal medicine
dc.subjectErythema multiforme
dc.subjectStevens Johnson syndrome
dc.subjectStevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome
dc.subjectToll like receptor 9
dc.subjectPolymorphism
dc.subjectSingle-nucleotide polymorphisms
dc.subjectSystemic-lupus-erythematosus
dc.subjectDermatological disease
dc.subjectGene polymorphism
dc.subjectJapanese patients
dc.subjectDrosophila toll
dc.subjectAssociation
dc.subjectTlr9
dc.subjectSusceptibility
dc.subjectDna
dc.subject.emtreeToll like receptor 9
dc.subject.emtreeAdolescent
dc.subject.emtreeAdult
dc.subject.emtreeAged
dc.subject.emtreeArticle
dc.subject.emtreeChild
dc.subject.emtreeErythema multiforme
dc.subject.emtreeFemale
dc.subject.emtreeGenetic polymorphism
dc.subject.emtreeGenetics
dc.subject.emtreeGenotype
dc.subject.emtreeHuman
dc.subject.emtreeImmunology
dc.subject.emtreeMale
dc.subject.emtreeMiddle aged
dc.subject.emtreeReverse transcription polymerase chain reaction
dc.subject.emtreeStevens Johnson syndrome
dc.subject.emtreeToxic epidermal necrolysis
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshChild
dc.subject.meshEpidermal necrolysis, toxic
dc.subject.meshErythema multiforme
dc.subject.meshFemale
dc.subject.meshGenotype
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshPolymorphism, genetic
dc.subject.meshReverse transcriptase polymerase chain reaction
dc.subject.meshStevens-Johnson syndrome
dc.subject.meshToll-like receptor 9
dc.subject.meshYoung adult
dc.subject.scopusStevens-Johnson Syndrome; Erythema Multiforme; Acute Generalized Exanthematous Pustulosis
dc.subject.wosMedicine, general & internal
dc.titleToll-like receptor 9 polymorphism in patients with erythema multiforme, Stevens Johnson syndrome and Stevens Johnson syndrome/toxic epidermal necrolysis overlap syndrome
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Genetik Tıp Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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