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dc.contributor.authorLima, Dhêmerson Souza de-
dc.contributor.authorOgusku, Maurício Morishi-
dc.contributor.authorSantos, Maria Cristina dos-
dc.contributor.authorSilva, Cláudia Maria de Melo-
dc.contributor.authorAlmeida, Vanessa Alves de-
dc.contributor.authorAntunes, Irineide Assumpção-
dc.contributor.authorBoechat, Antonio Luiz-
dc.contributor.authorRamasawmy, Rajendranath-
dc.contributor.authorSadahiro, Aya-
dc.date.accessioned2020-04-24T17:00:24Z-
dc.date.available2020-04-24T17:00:24Z-
dc.date.issued2016-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/14691-
dc.description.abstractImmunogenetic host factors are associated with susceptibility or protection to tuberculosis (TB). Strong associations of HLA class II genes with TB are reported. We analyzed the HLA-DRB1∗04 alleles to identify subtypes associated with pulmonary TB and their interaction with risk factors such as alcohol, smoking, and gender in 316 pulmonary TB patients and 306 healthy individuals from the Brazilian Amazon. The HLA-DRB1∗04 was prevalent in patients with pulmonary TB (p<0.0001; OR = 2.94; 95% CI = 2.12 to 4.08). Direct nucleotide sequencing of DRB1 exon 2 identified nine subtypes of HLA-DRB1∗04. The subtype HLA-DRB1∗04:11:01 (p = 0.0019; OR = 2.23; 95% CI = 1.34 to 3.70) was associated with susceptibility to pulmonary TB while DRB1∗04:07:01 (p<0.0001; OR = 0.02; 95% CI = 0.001 to 0.33) to protection. Notably, the interaction between alcohol and HLA-DRB1∗04:11:01 increased the risk for developing pulmonary TB (p = 0.0001; OR = 51.3; 95% CI = 6.81 to 386). Multibacillary pulmonary TB, the clinical presentation of disease transmission, was strongly associated with interaction to alcohol (p = 0.0026; OR = 11.1; 95% CI = 3.99 to 30.9), HLA-DRB1∗04:11:01 (p = 0.0442; OR =2.01; 95% CI = 1.03 to 3.93) and DRB1∗04:92 (p = 0.0112; OR = 8.62; 95% CI = 1.63 to 45.5). These results show that HLA-DRB1∗04 are associated with pulmonary TB. Interestingly, three subtypes, DRB1∗04:07:01, DRB1∗04:11:01 and DRB1∗04:92 of the HLA-DRB1∗04 could be potential immunogenetic markers that may help to explain mechanisms involved in disease development. © 2016 Souza de Lima et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 11, Número 2pt_BR
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subjectEarly Secretory Antigenic Target 6en
dc.subjectHla Drb1 Antigenen
dc.subjectHla Drb1 Antigenen
dc.subjectHla-drb1*04 Antigenen
dc.subjectAdulten
dc.subjectAlcohol Consumptionen
dc.subjectAlleleen
dc.subjectBrazilianen
dc.subjectControlled Studyen
dc.subjectCorrelation Analysisen
dc.subjectDisease Transmissionen
dc.subjectFemaleen
dc.subjectGenderen
dc.subjectGene Frequencyen
dc.subjectGenetic Associationen
dc.subjectGenetic Susceptibilityen
dc.subjectHla Drb1 Geneen
dc.subjectHumanen
dc.subjectLung Tuberculosisen
dc.subjectMajor Clinical Studyen
dc.subjectMaleen
dc.subjectNucleotide Sequenceen
dc.subjectPolymerase Chain Reactionen
dc.subjectPrevalenceen
dc.subjectSmokingen
dc.subjectAlleleen
dc.subjectPolymorphism, Geneticen
dc.subjectGenetic Predispositionen
dc.subjectGeneticsen
dc.subjectLung Tuberculosisen
dc.subjectMiddle Ageden
dc.subjectYoung Adulten
dc.subjectAdulten
dc.subjectAllelesen
dc.subjectFemaleen
dc.subjectGenetic Predisposition To Diseaseen
dc.subjectHla-drb1 Chainsen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectPolymorphism, Geneticen
dc.subjectTuberculosis, Pulmonaryen
dc.subjectYoung Adulten
dc.titleAlleles of HLA-DRB1∗04 associated with pulmonary tuberculosis in Amazon Brazilian populationen
dc.typeArtigopt_BR
dc.identifier.doi10.1371/journal.pone.0147543-
dc.publisher.journalPLoS ONEpt_BR
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