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Association of cytokine gene polymorphisms and serum concentrations with the outcome of chronic hepatitis B
Authors:Simone R.S. Conde  Rosimar N.M. Feitosa  Felipe Bonfim Freitas  Renata B. Hermes  Samia Demachki  Marialva T.F. Araújo  Manoel C.P. Soares  Ricardo Ishak  Antonio C.R. Vallinoto
Affiliation:1. Federal University of Para, Institute of Biological Sciences, Virus Laboratory, Belém, Pará, Brazil;2. Hospital Santa Casa de Misericórdia do Pará Foundation, Belém, Pará, Brazil;3. Instituto Evandro Chagas Institute, Laboratory of Hepatology, Belém, Pará, Brazil
Abstract:ObjectiveThe present paper investigated possible correlations between the clinical presentation of hepatitis B and the TNF-α ?308G/A, IFN-γ +874A/T, TGF-beta1 ?509C/T, and IL-10 ?1081A/G polymorphisms and associated serum levels of these cytokines.MethodsFifty-three hepatitis patients were selected and divided into two groups: A – inactive (n = 30) and B – chronic hepatitis/cirrhosis (n = 23). The control group consisted of 100 subjects who were positive for anti-HBc and anti-HBs. The serum concentrations of the cytokines were determined by immunoenzymatic assays. The polymorphisms of the cytokines genes were assessed by PCR and PCR-SSP.ResultsThe mean serum levels of IFN-γ of the control group were significantly higher than those of groups A and B, whereas the mean levels TGF-beta1 were significantly higher in groups A and B in comparison with the control. In the case of IL-10, the mean serum level recorded in the control group was significantly higher than that of group B. The TNF-α ?308AG genotype was considerably more frequent in group B (43.3%) than the control (14.4%).ConclusionHigher serum levels of IFN-γ and TGF-beta1 were associated with chronic hepatitis B, and lower serum levels of IL-10 were found in patients with the active disease. Furthermore the presence of allele A of the TNF-α ?308 polymorphism suggest a risk of the progressive disease.
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