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dc.contributor.authorHajilooi, M
dc.contributor.authorSardarian, K
dc.contributor.authorDadmanesh, M
dc.contributor.authorMatini, M
dc.contributor.authorLotfi, P
dc.contributor.authorBazmani, A
dc.contributor.authorTabatabaiefar, MA
dc.contributor.authorArababadi, MK
dc.contributor.authorMomeni, M
dc.date.accessioned2018-08-26T08:59:19Z
dc.date.available2018-08-26T08:59:19Z
dc.date.issued2013
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54795
dc.description.abstractPrevious investigations demonstrated that immune responses play critical roles in the defense against visceral leishmaniasis (VL). A key regulator of immune responses is the cytokine, IL-10 and polymorphisms within its promoter which could alter its expression. Thus, the aim of this study was to examine the correlation between polymorphism at the -819 position of the IL-10 gene and VL in a selected Iranian population. This cross-sectional study was performed on 100 patients with clinical presentation of VL and seropositive for the leishmania (group 1), 62 patients without clinical presentation but seropositive (group 2), and 128 healthy controls (group 3). The IL-10 -819 polymorphism was evaluated using the PCR-RFLP technique. The anti-leishmania antibody titration was assessed using an immunofluorescence assay. Our results showed that the polymorphism at IL-10 -819 (C/T) position was significantly associated with VL, and C/T genotype was significantly higher in VL patients when compared to groups 2 and 3 (p < 0.001). However, the results demonstrated that the C and T alleles were not associated with VL (p = 0.855). The data presented here confirm the results of previous reports that polymorphisms at the -819 position of the IL-10 gene can influence susceptibility to VL suggesting that the C/T genotype may be considered as a risk factor for the disease. é 2013 Springer Science+Business Media New York.
dc.language.isoEnglish
dc.relation.ispartofInflammation
dc.subjectbacterium antibody
dc.subjectinterleukin 10
dc.subjectadult
dc.subjectallele
dc.subjectantibody titer
dc.subjectarticle
dc.subjectclinical feature
dc.subjectcontrolled study
dc.subjectcross-sectional study
dc.subjectethnic group
dc.subjectfemale
dc.subjectgenetic association
dc.subjectgenetic polymorphism
dc.subjectgenetic predisposition
dc.subjectgenotype
dc.subjecthuman
dc.subjectimmunofluorescence test
dc.subjectinterleukin 10 gene
dc.subjectIranian
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmolecular pathology
dc.subjectpolymerase chain reaction
dc.subjectrestriction fragment length polymorphism
dc.subjectrisk factor
dc.subjectvisceral leishmaniasis
dc.subjectAdult
dc.subjectAntibodies, Protozoan
dc.subjectCross-Sectional Studies
dc.subjectFemale
dc.subjectGene Frequency
dc.subjectGenetic Association Studies
dc.subjectGenetic Predisposition to Disease
dc.subjectGenotype
dc.subjectHumans
dc.subjectInterleukin-10
dc.subjectIran
dc.subjectLeishmania
dc.subjectLeishmaniasis, Visceral
dc.subjectMale
dc.subjectPolymorphism, Single Nucleotide
dc.subjectPromoter Regions, Genetic
dc.subjectRisk Factors
dc.subjectYoung Adult
dc.titleIs the IL-10 -819 polymorphism associated with visceral leishmaniasis?
dc.typeArticle
dc.citation.volume36
dc.citation.issue6
dc.citation.spage1513
dc.citation.epage1518
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1007/s10753-013-9693-0


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