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Provedor de dados:  Genet. Mol. Biol.
País:  Brazil
Título:  Interferon lambda 4 (IFNL4) gene polymorphism is associated with spontaneous clearance of HCV in HIV-1 positive patients
Autores:  Alves,Camila Fernanda da Silveira
Grott,Camila Schultz
Lunge,Vagner Ricardo
Béria,Jorge Umberto
Tietzmann,Daniela Cardoso
Stein,Airton Tetelbom
Simon,Daniel
Data:  2016-09-01
Ano:  2016
Palavras-chave:  IFNL4 genotypes
HIV/HCV co-infected patients
Spontaneous clearance
Resumo:  Abstract Approximately one-third of the individuals infected with human immunodeficiency virus type 1 (HIV-1) are co-infected with hepatitis C virus (HCV). Co-infected patients have an increased risk for developing end-stage liver diseases. Variants upstream of the IFNL3 gene have been associated with spontaneous and treatment-induced clearance of HCV infection. Recently, a novel polymorphism was discovered, denoted IFNL4 ΔG > TT (rs368234815), which seems to be a better predictor of spontaneous clearance than the IFNL4 rs12979860 polymorphism. We aimed to determine the prevalence of the IFNL4 ΔG > TT variants and to evaluate the association with spontaneous clearance of HCV infection in Brazilian HIV-1 patients. The IFNL4 ΔG > TT genotypes were analyzed by polymerase chain reaction followed by restriction digestion in 138 HIV-1 positive patients who had an anti-HCV positive result. Spontaneous clearance of HCV was observed in 34 individuals (24.6%). IFNL4 genotype distribution was significantly different between individuals who had spontaneous clearance and chronic HCV patients (p=0.002). The probability of spontaneous clearance of HCV infection for patients with the IFNL4 TT/TT genotype was 3.6 times higher than for patients carrying the IFNL4 ΔG allele (OR=3.63, 95% CI:1.51-8.89, p=0.001). The IFNL4 ΔG > TT polymorphism seems to be better than IFNL4 rs12979860 to predict spontaneous clearance of the HCV in Brazilian HIV-1 positive patients.
Tipo:  Info:eu-repo/semantics/other
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572016000300374
Editor:  Sociedade Brasileira de Genética
Relação:  10.1590/1678-4685-GMB-2015-0106
Formato:  text/html
Fonte:  Genetics and Molecular Biology v.39 n.3 2016
Direitos:  info:eu-repo/semantics/openAccess
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