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dc.contributor.authorSilva, George Allan Villarouco da-
dc.contributor.authorRamasawmy, Rajendranath-
dc.contributor.authorBoechat, Antonio Luiz-
dc.contributor.authorMorais, A. C.-
dc.contributor.authorCarvalho, B. K.S.-
dc.contributor.authorSousa, K. B A-
dc.contributor.authorSouza, V. C.-
dc.contributor.authorCunha, Maria Coelho Graça Souza-
dc.contributor.authorBarletta-Naveca, Raphaela Honorato-
dc.contributor.authorSantos, M. P.-
dc.contributor.authorNaveca, Felipe Gomes-
dc.date.accessioned2020-06-15T21:48:05Z-
dc.date.available2020-06-15T21:48:05Z-
dc.date.issued2015-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/17493-
dc.description.abstractPolymorphisms present in the TNF promoter region has shown to influence the gene transcription. Leprosy displays different clinical manifestations according to the immune responses of the individual infected with Mycobacterium leprae. In this study, we evaluated the single nucleotide polymorphisms (SNPs) -238 G/A (rs361525), -308 G/A (rs1800629), -857 C/T (rs1799724), -863 A/C (rs1800630) and -1031 T/C (rs1799964) in the promoter region of the TNF to see whether these SNPs influence host-susceptibility to leprosy and the different clinical manifestation. Nucleotide sequencing was performed with DNA samples from 108 leprosy patients and 253 control subjects. An association between -1031 C/C genotype and protection from leprosy was observed when leprosy patients were compared to controls (OR 0.11; 95% CI. =. 0.01-0.82; p=. 0.012). The -857 C/T genotype may be associated with susceptibility to leprosy (OR. =. 1.81; 95% CI. =. 1.09-3.00; p=. 0.028). Similar genotype and allele frequencies for the SNPs -308 G/A and -238 G/A were observed between leprosy patients and control subjects. Altogether, TNF polymorphisms in the promoter region may be predictive of leprosy outcome. © 2015 American Society for Histocompatibility and Immunogenetics.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 76, Número 2-3, Pags. 137-141pt_BR
dc.rightsRestrito*
dc.subjectDnaen
dc.subjectNucleotideen
dc.subjectTumor Necrosis Factoren
dc.subjectBiological Markeren
dc.subjectTumor Necrosis Factor-alphaen
dc.subjectAmazonaen
dc.subjectControlled Studyen
dc.subjectFemaleen
dc.subjectGene Frequencyen
dc.subjectGenetic Associationen
dc.subjectGenotypeen
dc.subjectHost Susceptibilityen
dc.subjectHumanen
dc.subjectLeprosyen
dc.subjectMajor Clinical Studyen
dc.subjectMaleen
dc.subjectOutcome Assessmenten
dc.subjectPriority Journalen
dc.subjectPromoter Regionen
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectDisease Courseen
dc.subjectGenetic Associationen
dc.subjectGenetic Predispositionen
dc.subjectGeneticsen
dc.subjectGenotypeen
dc.subjectImmunologyen
dc.subjectLeprosyen
dc.subjectMetabolismen
dc.subjectMycobacterium Lepraeen
dc.subjectNucleotide Sequenceen
dc.subjectPredictive Valueen
dc.subjectPromoter Regionen
dc.subjectBiomarkersen
dc.subjectDisease Progressionen
dc.subjectDna Mutational Analysisen
dc.subjectGene Frequencyen
dc.subjectGenetic Association Studiesen
dc.subjectGenetic Predisposition To Diseaseen
dc.subjectGenotypeen
dc.subjectHumansen
dc.subjectLeprosyen
dc.subjectMycobacterium Lepraeen
dc.subjectPolymorphism, Single Nucleotideen
dc.subjectPredictive Value Of Testsen
dc.subjectPromoter Regions, Geneticen
dc.subjectTumor Necrosis Factor-alphaen
dc.titleAssociation of TNF -1031 C/C as a potential protection marker for leprosy development in Amazonas state patients, Brazilen
dc.typeArtigopt_BR
dc.identifier.doi10.1016/j.humimm.2015.01.011-
dc.publisher.journalHuman Immunologypt_BR
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