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IL28B Is Associated with Outcomes of Chronic HBV Infection

PURPOSE: The role of IL28B gene variants and expression in hepatitis B virus (HBV) infections are not well understood. Here, we evaluated whether IL28B gene expression and rs12979860 variations are associated with HBV outcomes. MATERIALS AND METHODS: IL28B genetic variations (rs12979860) were genoty...

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Autores principales: Shi, Xiaodong, Chi, Xiumei, Pan, Yu, Gao, Yanhang, Li, Wanyu, Yang, Chen, Zhong, Jin, Xu, Damo, Zhang, Manna, Minuk, Gerald, Jiang, Jing, Niu, Junqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397430/
https://www.ncbi.nlm.nih.gov/pubmed/25837166
http://dx.doi.org/10.3349/ymj.2015.56.3.625
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author Shi, Xiaodong
Chi, Xiumei
Pan, Yu
Gao, Yanhang
Li, Wanyu
Yang, Chen
Zhong, Jin
Xu, Damo
Zhang, Manna
Minuk, Gerald
Jiang, Jing
Niu, Junqi
author_facet Shi, Xiaodong
Chi, Xiumei
Pan, Yu
Gao, Yanhang
Li, Wanyu
Yang, Chen
Zhong, Jin
Xu, Damo
Zhang, Manna
Minuk, Gerald
Jiang, Jing
Niu, Junqi
author_sort Shi, Xiaodong
collection PubMed
description PURPOSE: The role of IL28B gene variants and expression in hepatitis B virus (HBV) infections are not well understood. Here, we evaluated whether IL28B gene expression and rs12979860 variations are associated with HBV outcomes. MATERIALS AND METHODS: IL28B genetic variations (rs12979860) were genotyped by pyrosequencing of DNA samples from 137 individuals with chronic HBV infection [50 inactive carriers (IC), 34 chronic hepatitis B (CHB), 27 cirrhosis, 26 hepatocellular carcinoma (HCC)], and 19 healthy controls. IL28A/B mRNA expression in peripheral blood mononuclear cells was determined by qRT-PCR, and serum IL28B protein was measured by ELISA. RESULTS: Patients with IL28B C/C genotype had greater IL28A/B mRNA expression and higher IL28B protein levels than C/T patients. Within the various disease stages, compared to IC and healthy controls, IL28B expression was reduced in the CHB, cirrhosis, and HCC cohorts (CHB vs. IC, p=0.02; cirrhosis vs. IC, p=0.01; HCC vs. IC, p=0.001; CHB vs. controls, p<0.01; cirrhosis vs. controls, p<0.01; HCC vs. controls, p<0.01). When stratified with respect to serum HBV markers in the IC and CHB cohorts, IL28B mRNA and protein levels were higher in HBeAg-positive than negative individuals (p=0.01). Logistic regression analysis revealed that factors associated with high IL28B protein levels were C/C versus C/T genotype [p=0.016, odds ratio (OR)=0.25, 95% confidence interval (CI)=0.08-0.78], high alanine aminotransferase values (p<0.001, OR=8.02, 95% CI=2.64-24.4), and the IC stage of HBV infection (p<0.001). CONCLUSION: Our data suggest that IL28B genetic variations may play an important role in long-term development of disease in chronic HBV infections.
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spelling pubmed-43974302015-05-01 IL28B Is Associated with Outcomes of Chronic HBV Infection Shi, Xiaodong Chi, Xiumei Pan, Yu Gao, Yanhang Li, Wanyu Yang, Chen Zhong, Jin Xu, Damo Zhang, Manna Minuk, Gerald Jiang, Jing Niu, Junqi Yonsei Med J Original Article PURPOSE: The role of IL28B gene variants and expression in hepatitis B virus (HBV) infections are not well understood. Here, we evaluated whether IL28B gene expression and rs12979860 variations are associated with HBV outcomes. MATERIALS AND METHODS: IL28B genetic variations (rs12979860) were genotyped by pyrosequencing of DNA samples from 137 individuals with chronic HBV infection [50 inactive carriers (IC), 34 chronic hepatitis B (CHB), 27 cirrhosis, 26 hepatocellular carcinoma (HCC)], and 19 healthy controls. IL28A/B mRNA expression in peripheral blood mononuclear cells was determined by qRT-PCR, and serum IL28B protein was measured by ELISA. RESULTS: Patients with IL28B C/C genotype had greater IL28A/B mRNA expression and higher IL28B protein levels than C/T patients. Within the various disease stages, compared to IC and healthy controls, IL28B expression was reduced in the CHB, cirrhosis, and HCC cohorts (CHB vs. IC, p=0.02; cirrhosis vs. IC, p=0.01; HCC vs. IC, p=0.001; CHB vs. controls, p<0.01; cirrhosis vs. controls, p<0.01; HCC vs. controls, p<0.01). When stratified with respect to serum HBV markers in the IC and CHB cohorts, IL28B mRNA and protein levels were higher in HBeAg-positive than negative individuals (p=0.01). Logistic regression analysis revealed that factors associated with high IL28B protein levels were C/C versus C/T genotype [p=0.016, odds ratio (OR)=0.25, 95% confidence interval (CI)=0.08-0.78], high alanine aminotransferase values (p<0.001, OR=8.02, 95% CI=2.64-24.4), and the IC stage of HBV infection (p<0.001). CONCLUSION: Our data suggest that IL28B genetic variations may play an important role in long-term development of disease in chronic HBV infections. Yonsei University College of Medicine 2015-05-01 2015-04-01 /pmc/articles/PMC4397430/ /pubmed/25837166 http://dx.doi.org/10.3349/ymj.2015.56.3.625 Text en © Copyright: Yonsei University College of Medicine 2015 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Shi, Xiaodong
Chi, Xiumei
Pan, Yu
Gao, Yanhang
Li, Wanyu
Yang, Chen
Zhong, Jin
Xu, Damo
Zhang, Manna
Minuk, Gerald
Jiang, Jing
Niu, Junqi
IL28B Is Associated with Outcomes of Chronic HBV Infection
title IL28B Is Associated with Outcomes of Chronic HBV Infection
title_full IL28B Is Associated with Outcomes of Chronic HBV Infection
title_fullStr IL28B Is Associated with Outcomes of Chronic HBV Infection
title_full_unstemmed IL28B Is Associated with Outcomes of Chronic HBV Infection
title_short IL28B Is Associated with Outcomes of Chronic HBV Infection
title_sort il28b is associated with outcomes of chronic hbv infection
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397430/
https://www.ncbi.nlm.nih.gov/pubmed/25837166
http://dx.doi.org/10.3349/ymj.2015.56.3.625
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