Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection

With the aim of investigating whether interleukin 28B gene (IL28B) rs1297860 polymorphism is associated with different hepatitis C (HCV) infection statuses, we compared IL28B allelic distribution in an Italian case series of 1050 patients with chronic infection and different outco...

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Main Authors: Valli De Re, Laura Gragnani, Elisa Fognani, Alessia Piluso, Francesco Izzo, Alessandra Mangia, Marina Crovatto, Graziella Gava, Pietro Casarin, Domenico Sansonno, Vito Racanelli, Salvatore De Vita, Pietro Pioltelli, Laura Caggiari, Mariangela De Zorzi, Massimiliano Berretta, Andrea Gini, Antonella Zucchetto, Franco Maria Buonaguro, Paolo De Paoli, Anna Linda Zignego
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/710642
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author Valli De Re
Laura Gragnani
Elisa Fognani
Alessia Piluso
Francesco Izzo
Alessandra Mangia
Marina Crovatto
Graziella Gava
Pietro Casarin
Domenico Sansonno
Vito Racanelli
Salvatore De Vita
Pietro Pioltelli
Laura Caggiari
Mariangela De Zorzi
Massimiliano Berretta
Andrea Gini
Antonella Zucchetto
Franco Maria Buonaguro
Paolo De Paoli
Anna Linda Zignego
spellingShingle Valli De Re
Laura Gragnani
Elisa Fognani
Alessia Piluso
Francesco Izzo
Alessandra Mangia
Marina Crovatto
Graziella Gava
Pietro Casarin
Domenico Sansonno
Vito Racanelli
Salvatore De Vita
Pietro Pioltelli
Laura Caggiari
Mariangela De Zorzi
Massimiliano Berretta
Andrea Gini
Antonella Zucchetto
Franco Maria Buonaguro
Paolo De Paoli
Anna Linda Zignego
Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
BioMed Research International
author_facet Valli De Re
Laura Gragnani
Elisa Fognani
Alessia Piluso
Francesco Izzo
Alessandra Mangia
Marina Crovatto
Graziella Gava
Pietro Casarin
Domenico Sansonno
Vito Racanelli
Salvatore De Vita
Pietro Pioltelli
Laura Caggiari
Mariangela De Zorzi
Massimiliano Berretta
Andrea Gini
Antonella Zucchetto
Franco Maria Buonaguro
Paolo De Paoli
Anna Linda Zignego
author_sort Valli De Re
title Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
title_short Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
title_full Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
title_fullStr Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
title_full_unstemmed Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
title_sort impact of immunogenetic il28b polymorphism on natural outcome of hcv infection
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2014-01-01
description With the aim of investigating whether interleukin 28B gene (IL28B) rs1297860 polymorphism is associated with different hepatitis C (HCV) infection statuses, we compared IL28B allelic distribution in an Italian case series of 1050 patients with chronic infection and different outcomes, 47 individuals who spontaneously cleared HCV, and 178 blood donors. Furthermore, we compared IL28B variants among 3882 Caucasian patients with chronic infection, 397 with spontaneous clearance, and 1366 blood donors reported in PubMed. Overall data confirmed a relation between IL28B C allele and HCV spontaneous clearance. Furthermore, we found that IL28B T allele had a weak relation with chronic HCV progression to hepatocellular carcinoma. Study findings are in accordance with the hepatocellular carcinogenic model where IL28B TT genotype, by promoting a persistent chronic hepatitis which leads to both hepatocyte injury and chronic inflammation, could facilitate HCC development. Conversely, patients with lymphoproliferative disorders had not any significantly different IL28B rs1297860 allelic distribution than those with chronic HCV, but, like all chronic HCV-related diseases, they showed a lower CC frequency than patients who spontaneously cleared HCV. Study results confirmed the model of persistent HCV infection as a risk factor for the pathogenesis of both liver and lymphoproliferative disorders.
url http://dx.doi.org/10.1155/2014/710642
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spelling doaj-790c072c79c4492ca02a838a3af3b50b2020-11-24T21:37:02ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/710642710642Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV InfectionValli De Re0Laura Gragnani1Elisa Fognani2Alessia Piluso3Francesco Izzo4Alessandra Mangia5Marina Crovatto6Graziella Gava7Pietro Casarin8Domenico Sansonno9Vito Racanelli10Salvatore De Vita11Pietro Pioltelli12Laura Caggiari13Mariangela De Zorzi14Massimiliano Berretta15Andrea Gini16Antonella Zucchetto17Franco Maria Buonaguro18Paolo De Paoli19Anna Linda Zignego20Bio-Proteomics Facility, Department of Translational Research, CRO, National Cancer Institute, 33081 Aviano, ItalyInterdepartmental Center for Systemic Manifestations of Hepatitis Virus MASVE, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, ItalyInterdepartmental Center for Systemic Manifestations of Hepatitis Virus MASVE, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, ItalyInterdepartmental Center for Systemic Manifestations of Hepatitis Virus MASVE, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, ItalyHepatobiliary Unit, National Cancer Institute “Fondazione Pascale”, 80138 Naples, ItalyLiver Unit, IRCCS Casa Sollievo della Sofferenza Hospital, 71013 San Giovanni Rotondo, ItalyCytogenetics and Molecular Biology Unit, Santa Maria degli Angeli Hospital Pordenone, 33170 Pordenone, ItalyCytogenetics and Molecular Biology Unit, Santa Maria degli Angeli Hospital Pordenone, 33170 Pordenone, ItalyInternal Medicine-Liver Unit, Santa Maria degli Angeli Hospital Pordenone, 33170 Pordenone, ItalyImmunology Section, Department of Biomedical Sciences and Human Oncology, University of Bari Medical School, 70121 Bari, ItalyImmunology Section, Department of Biomedical Sciences and Human Oncology, University of Bari Medical School, 70121 Bari, ItalyClinic of Rheumatology, Department of Medical and Biological Sciences, University Hospital Santa Maria della Misericordia, 33100 Udine, ItalyHematology and Transplant Unit, San Gerardo Hospital, University of Milano-Bicocca, Monza, ItalyBio-Proteomics Facility, Department of Translational Research, CRO, National Cancer Institute, 33081 Aviano, ItalyBio-Proteomics Facility, Department of Translational Research, CRO, National Cancer Institute, 33081 Aviano, ItalyMedical Oncology, Centro di Riferimento Oncologico, 33081 Aviano, Pordenone, ItalyEpidemiology and Biostatistics, Centro di Riferimento Oncologico, IRCCS, 33081 Aviano, ItalyEpidemiology and Biostatistics, Centro di Riferimento Oncologico, IRCCS, 33081 Aviano, ItalyMolecular Biology and Viral Oncology, National Cancer Institute “Fondazione Pascale”, 80138 Naples, ItalyBio-Proteomics Facility, Department of Translational Research, CRO, National Cancer Institute, 33081 Aviano, ItalyInterdepartmental Center for Systemic Manifestations of Hepatitis Virus MASVE, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, ItalyWith the aim of investigating whether interleukin 28B gene (IL28B) rs1297860 polymorphism is associated with different hepatitis C (HCV) infection statuses, we compared IL28B allelic distribution in an Italian case series of 1050 patients with chronic infection and different outcomes, 47 individuals who spontaneously cleared HCV, and 178 blood donors. Furthermore, we compared IL28B variants among 3882 Caucasian patients with chronic infection, 397 with spontaneous clearance, and 1366 blood donors reported in PubMed. Overall data confirmed a relation between IL28B C allele and HCV spontaneous clearance. Furthermore, we found that IL28B T allele had a weak relation with chronic HCV progression to hepatocellular carcinoma. Study findings are in accordance with the hepatocellular carcinogenic model where IL28B TT genotype, by promoting a persistent chronic hepatitis which leads to both hepatocyte injury and chronic inflammation, could facilitate HCC development. Conversely, patients with lymphoproliferative disorders had not any significantly different IL28B rs1297860 allelic distribution than those with chronic HCV, but, like all chronic HCV-related diseases, they showed a lower CC frequency than patients who spontaneously cleared HCV. Study results confirmed the model of persistent HCV infection as a risk factor for the pathogenesis of both liver and lymphoproliferative disorders.http://dx.doi.org/10.1155/2014/710642