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Interferon Alpha-2b Therapy in Chronic Hepatitis Delta

BACKGROUND: Approximately 5% of hepatitis B virus (HBV) carriers are coinfected with hepatitis D virus (HDV). HBV/HDV coinfection is a major cause of cirrhosis and end stage liver disease in chronic HBsAg carriers. The only approved therapy for chronic hepatitis delta is interferon alpha (IFN α) in...

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Autores principales: Keshvari, Maryam, Alavian, Seyed Moayed, Sharafi, Heidar, Karimi, Gharib, Gholami Fesharaki, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989544/
https://www.ncbi.nlm.nih.gov/pubmed/24744790
http://dx.doi.org/10.5812/hepatmon.15729
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author Keshvari, Maryam
Alavian, Seyed Moayed
Sharafi, Heidar
Karimi, Gharib
Gholami Fesharaki, Mohammad
author_facet Keshvari, Maryam
Alavian, Seyed Moayed
Sharafi, Heidar
Karimi, Gharib
Gholami Fesharaki, Mohammad
author_sort Keshvari, Maryam
collection PubMed
description BACKGROUND: Approximately 5% of hepatitis B virus (HBV) carriers are coinfected with hepatitis D virus (HDV). HBV/HDV coinfection is a major cause of cirrhosis and end stage liver disease in chronic HBsAg carriers. The only approved therapy for chronic hepatitis delta is interferon alpha (IFN α) in either pegylated or conventional forms. Although higher doses and longer durations of IFN α therapy in HBV/HDV coinfected patients are currently applied, yet treatment response is low. OBJECTIVES: We aimed to determine the efficacy of IFN α-2b therapy in patients with HBV/HDV coinfection. PATIENTS AND METHODS: In this cross sectional study, 20 HBsAg carriers with positive Anti-HDVAb and RT-PCR for HDV RNA were recruited and treated for three year duration with 5 million units (MU) of IFN α-2b, three times weekly or one year with 5 MU of IFN α-2b daily. Sustained virological response (SVR) was defined as a negative qualitative HDV RT-PCR, 6 months after treatment cessation. RESULTS: Overall, 3 (15%) subjects achieved SVR, 10 cases (50%) relapsed after treatment cessation and 7 (35%) patients did not clear HDV during the treatment. CONCLUSIONS: HDV coinfection with HBV had very low response rate to high doses and long durations of IFN α-2b therapy.
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spelling pubmed-39895442014-04-17 Interferon Alpha-2b Therapy in Chronic Hepatitis Delta Keshvari, Maryam Alavian, Seyed Moayed Sharafi, Heidar Karimi, Gharib Gholami Fesharaki, Mohammad Hepat Mon Research Article BACKGROUND: Approximately 5% of hepatitis B virus (HBV) carriers are coinfected with hepatitis D virus (HDV). HBV/HDV coinfection is a major cause of cirrhosis and end stage liver disease in chronic HBsAg carriers. The only approved therapy for chronic hepatitis delta is interferon alpha (IFN α) in either pegylated or conventional forms. Although higher doses and longer durations of IFN α therapy in HBV/HDV coinfected patients are currently applied, yet treatment response is low. OBJECTIVES: We aimed to determine the efficacy of IFN α-2b therapy in patients with HBV/HDV coinfection. PATIENTS AND METHODS: In this cross sectional study, 20 HBsAg carriers with positive Anti-HDVAb and RT-PCR for HDV RNA were recruited and treated for three year duration with 5 million units (MU) of IFN α-2b, three times weekly or one year with 5 MU of IFN α-2b daily. Sustained virological response (SVR) was defined as a negative qualitative HDV RT-PCR, 6 months after treatment cessation. RESULTS: Overall, 3 (15%) subjects achieved SVR, 10 cases (50%) relapsed after treatment cessation and 7 (35%) patients did not clear HDV during the treatment. CONCLUSIONS: HDV coinfection with HBV had very low response rate to high doses and long durations of IFN α-2b therapy. Kowsar 2014-03-01 /pmc/articles/PMC3989544/ /pubmed/24744790 http://dx.doi.org/10.5812/hepatmon.15729 Text en Copyright © 2014, Kowsar Corp. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Keshvari, Maryam
Alavian, Seyed Moayed
Sharafi, Heidar
Karimi, Gharib
Gholami Fesharaki, Mohammad
Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title_full Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title_fullStr Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title_full_unstemmed Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title_short Interferon Alpha-2b Therapy in Chronic Hepatitis Delta
title_sort interferon alpha-2b therapy in chronic hepatitis delta
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989544/
https://www.ncbi.nlm.nih.gov/pubmed/24744790
http://dx.doi.org/10.5812/hepatmon.15729
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