Association of cytokine gene polymorphisms and serum concentrations with the outcome of chronic hepatitis B.
Autor: | Conde SR; Federal University of Para, Institute of Biological Sciences, Virus Laboratory, Belém, Pará, Brazil., Feitosa RN, Freitas FB, Hermes RB, Demachki S, Araújo MT, Soares MC, Ishak R, Vallinoto AC |
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Jazyk: | angličtina |
Zdroj: | Cytokine [Cytokine] 2013 Mar; Vol. 61 (3), pp. 940-4. Date of Electronic Publication: 2013 Feb 08. |
DOI: | 10.1016/j.cyto.2013.01.004 |
Abstrakt: | Objective: The 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. Methods: Fifty-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. Results: The 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%). Conclusion: Higher 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. (Copyright © 2013 Elsevier Ltd. All rights reserved.) |
Databáze: | MEDLINE |
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