Author/Authors :
Zare، Fateme نويسنده Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. , , Hadinedoushan، Hossein نويسنده , , Akhondi-Meybodi، Mohsen نويسنده Gastrology Department, Faculty of Medicine, Shahid Sadoughi Hospital, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran , , Dehghanmanshadi، Mahdi نويسنده Department of Immunology, Reproductive Immunology Research
Center, Shahid Sadoughi University of Medical Sciences, Yazd, IR
Iran , , Mirghanizade-Bafghi، Seyyed Ali نويسنده Immunology Department, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran , , Vakili ، Mahmood نويسنده Department of Community Medicine, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran ,
Abstract :
The hepatitis C virus (HCV) is an important human pathogen
affecting an estimated 120 - 170 million individuals in the world.
Polymorphisms of the IL28B gene are strongly associated with sustained
virological response in patients with chronic hepatitis C treated with
peginterferon and ribavirin. The aims of this study were to compare the
allelic and genotypic frequencies of the IL28B rs12979860 polymorphism
in sustained virological response in patients who did not respond to the
standard of care treatment and to verify whether there is a correlation
between the viral load and the IL28B rs12979860 polymorphism. This
cross-sectional study was carried out on 75 HCV-infected patients,
including 45 responders to treatment (group 1) and 30 nonresponders
(group 2). We compared the allele and genotype frequencies of the IL28B
rs12979860 between the two groups using the PCR-RFLP method. The
genotype frequencies of rs12979860 polymorphism in group 1 were CC
(28.9%), CT (37.8%) and TT (33.3%) and in group 2 were CC (6.7%), CT
(43.3%) and TT (50%). There was a significant difference in genotype
frequencies of IL28B polymorphism between the two groups (P = 0.03).
There was no significant association between the viral load and IL28B
rs12979860 genotypes in either group 1 (P = 0.3) or group 2 (P = 0.2).
Our findings indicate that patients with the homozygous CC genotype in
the IL28B gene had a significantly higher rate of response to treatment
than those with the TT or CT genotypes. Nor does the IL28B rs12979860
polymorphism affect the viral load.