HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges

Several investigations have been published on Hepatitis Delta Virus (HDV) infection in recent years, from which we have drawn the salient data to provide readers with useful information to improve their knowledge on the subject. HDV genotypes 5–8 have been recently imported to Western countries from...

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Main Authors: Caterina Sagnelli, Evangelista Sagnelli, Antonio Russo, Mariantonietta Pisaturo, Laura Occhiello, Nicola Coppola
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Life
Subjects:
Online Access:https://www.mdpi.com/2075-1729/11/2/169
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author Caterina Sagnelli
Evangelista Sagnelli
Antonio Russo
Mariantonietta Pisaturo
Laura Occhiello
Nicola Coppola
author_facet Caterina Sagnelli
Evangelista Sagnelli
Antonio Russo
Mariantonietta Pisaturo
Laura Occhiello
Nicola Coppola
author_sort Caterina Sagnelli
collection DOAJ
description Several investigations have been published on Hepatitis Delta Virus (HDV) infection in recent years, from which we have drawn the salient data to provide readers with useful information to improve their knowledge on the subject. HDV genotypes 5–8 have been recently imported to Western countries from central Africa, whose clinical relevance deserves further investigation. Ongoing HDV replication has been identified as an independent predictor of progression to cirrhosis and HCC for patients with HDV chronic hepatitis (HDV-CH). Long-term treatments of HDV-CH with standard or pegylated interferon alfa (peg-IFN-α) have all been unsatisfactory, leading to a sustained virological response (SVR) only in 20–30% of patients treated, faced with a poor tolerability and frequent serious adverse reactions; the addition of HBV nucleo(s)tide analogues to peg-IFN- α did not improve the rate of SVR. The improved knowledge of the HDV life cycle has allowed the development of direct acting agents towards key-points of the HDV life cycle, namely bulevirtide, lonafarnib and nucleic acid polymers. Preliminary data have shown that these drugs are more effective than interferon-based therapies, but adverse reactions are also common, which however seem toned down in combination therapy with other antivirals.
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spelling doaj.art-80cb1933d3814a85bb095235116a2f592023-12-11T18:01:12ZengMDPI AGLife2075-17292021-02-0111216910.3390/life11020169HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future ChallengesCaterina Sagnelli0Evangelista Sagnelli1Antonio Russo2Mariantonietta Pisaturo3Laura Occhiello4Nicola Coppola5Department of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalyDepartment of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalyDepartment of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalyDepartment of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalyDepartment of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalyDepartment of Mental Health and Public Medicine, University of Campania “Luigi Vanvitelli”, 80131 Naples, ItalySeveral investigations have been published on Hepatitis Delta Virus (HDV) infection in recent years, from which we have drawn the salient data to provide readers with useful information to improve their knowledge on the subject. HDV genotypes 5–8 have been recently imported to Western countries from central Africa, whose clinical relevance deserves further investigation. Ongoing HDV replication has been identified as an independent predictor of progression to cirrhosis and HCC for patients with HDV chronic hepatitis (HDV-CH). Long-term treatments of HDV-CH with standard or pegylated interferon alfa (peg-IFN-α) have all been unsatisfactory, leading to a sustained virological response (SVR) only in 20–30% of patients treated, faced with a poor tolerability and frequent serious adverse reactions; the addition of HBV nucleo(s)tide analogues to peg-IFN- α did not improve the rate of SVR. The improved knowledge of the HDV life cycle has allowed the development of direct acting agents towards key-points of the HDV life cycle, namely bulevirtide, lonafarnib and nucleic acid polymers. Preliminary data have shown that these drugs are more effective than interferon-based therapies, but adverse reactions are also common, which however seem toned down in combination therapy with other antivirals.https://www.mdpi.com/2075-1729/11/2/169HDVhepatitis Depidemiologypathogenesistherapeutics
spellingShingle Caterina Sagnelli
Evangelista Sagnelli
Antonio Russo
Mariantonietta Pisaturo
Laura Occhiello
Nicola Coppola
HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
Life
HDV
hepatitis D
epidemiology
pathogenesis
therapeutics
title HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
title_full HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
title_fullStr HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
title_full_unstemmed HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
title_short HBV/HDV Co-Infection: Epidemiological and Clinical Changes, Recent Knowledge and Future Challenges
title_sort hbv hdv co infection epidemiological and clinical changes recent knowledge and future challenges
topic HDV
hepatitis D
epidemiology
pathogenesis
therapeutics
url https://www.mdpi.com/2075-1729/11/2/169
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