Hepatitis D medical therapy: Difference between revisions
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==Medical Therapy== | ==Medical Therapy== | ||
Currently there is no effective [[antiviral]] therapy available for treatment of acute or chronic hepatitis D.<ref>{{cite book | last = Fields | first = Bernard | title = Fields virology | publisher = Wolters Kluwer Health/Lippincott Williams & Wilkins | location = Philadelphia | year = 2013 | isbn = 9781451105636 }}</ref> | Currently there is no effective [[antiviral]] therapy available for treatment of acute or chronic hepatitis D.<ref>{{cite book | last = Fields | first = Bernard | title = Fields virology | publisher = Wolters Kluwer Health/Lippincott Williams & Wilkins | location = Philadelphia | year = 2013 | isbn = 9781451105636 }}</ref> | ||
The goal of treatment in hepatitis D is the clearance of [[HDV]] and [[HBV]] helper virus. The complexity of the treatment resides in the need to address both [[viruses]], and in the simplicity of the [[HDV]]. The fact that [[HDV]] uses the host cell's [[enzymes]] for replication limits the number of targets for therapeutic agents. | The goal of treatment in hepatitis D is the clearance of [[HDV]] and [[HBV]] helper virus. The complexity of the treatment resides in the need to address both [[viruses]], and in the simplicity of the [[HDV]]. The fact that [[HDV]] uses the host cell's [[enzymes]] for replication limits the number of targets for therapeutic agents.<ref name="HeidrichManns2012">{{cite journal|last1=Heidrich|first1=Benjamin|last2=Manns|first2=Michael P.|last3=Wedemeyer|first3=Heiner|title=Treatment Options for Hepatitis Delta Virus Infection|journal=Current Infectious Disease Reports|volume=15|issue=1|year=2012|pages=31–38|issn=1523-3847|doi=10.1007/s11908-012-0307-z}}</ref> | ||
Interferon-α is the only drug that has shown antiviral activity against HDV. Both forms of the drug (conventional and pegylated) are able to inhibit HDV replication cycle. | [[Interferon-α]] is the only drug that has shown antiviral activity against [[HDV]]. Both forms of the drug (conventional and pegylated) are able to inhibit HDV replication cycle.<ref name="HeidrichManns2012">{{cite journal|last1=Heidrich|first1=Benjamin|last2=Manns|first2=Michael P.|last3=Wedemeyer|first3=Heiner|title=Treatment Options for Hepatitis Delta Virus Infection|journal=Current Infectious Disease Reports|volume=15|issue=1|year=2012|pages=31–38|issn=1523-3847|doi=10.1007/s11908-012-0307-z}}</ref><ref name="FarciMandas1994">{{cite journal|last1=Farci|first1=Patrizia|last2=Mandas|first2=Antonella|last3=Coiana|first3=Alessandra|last4=Lai|first4=Maria Eliana|last5=Desmet|first5=Valeer|last6=Van Eyken|first6=Peter|last7=Gibo|first7=Yukio|last8=Caruso|first8=Luciano|last9=Scaccabarozzi|first9=Sergio|last10=Criscuolo|first10=Domenico|last11=Ryff|first11=Jean-Charles|last12=Balestrieri|first12=Angelo|title=Treatment of Chronic Hepatitis D with Interferon Alfa-2a|journal=New England Journal of Medicine|volume=330|issue=2|year=1994|pages=88–94|issn=0028-4793|doi=10.1056/NEJM199401133300202}}</ref> | ||
Despite some discrepancies among studies, relating to doses, forms and treatment durations of interferon-α, 25-40% of patients showed sustained response to treatment, 1 to 2 years after therapy. | |||
Revision as of 19:31, 6 August 2014
Hepatitis D |
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Hepatitis D medical therapy On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Varun Kumar, M.B.B.S. [2]; João André Alves Silva, M.D. [3] Jolanta Marszalek, M.D. [4]
Overview
Medical Therapy
Currently there is no effective antiviral therapy available for treatment of acute or chronic hepatitis D.[1] The goal of treatment in hepatitis D is the clearance of HDV and HBV helper virus. The complexity of the treatment resides in the need to address both viruses, and in the simplicity of the HDV. The fact that HDV uses the host cell's enzymes for replication limits the number of targets for therapeutic agents.[2]
Interferon-α is the only drug that has shown antiviral activity against HDV. Both forms of the drug (conventional and pegylated) are able to inhibit HDV replication cycle.[2][3]
Despite some discrepancies among studies, relating to doses, forms and treatment durations of interferon-α, 25-40% of patients showed sustained response to treatment, 1 to 2 years after therapy.
Liver transplantation has been helpful for treating fulminant acute and end-stage chronic hepatitis. In one study, the 5-year survival rate of transplant patients for terminal delta cirrhosis was 88% with reappearance of HBsAg only in 9% under long-term anti-HBs prophylaxis.[4]
References
- ↑ Fields, Bernard (2013). Fields virology. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. ISBN 9781451105636.
- ↑ 2.0 2.1 Heidrich, Benjamin; Manns, Michael P.; Wedemeyer, Heiner (2012). "Treatment Options for Hepatitis Delta Virus Infection". Current Infectious Disease Reports. 15 (1): 31–38. doi:10.1007/s11908-012-0307-z. ISSN 1523-3847.
- ↑ Farci, Patrizia; Mandas, Antonella; Coiana, Alessandra; Lai, Maria Eliana; Desmet, Valeer; Van Eyken, Peter; Gibo, Yukio; Caruso, Luciano; Scaccabarozzi, Sergio; Criscuolo, Domenico; Ryff, Jean-Charles; Balestrieri, Angelo (1994). "Treatment of Chronic Hepatitis D with Interferon Alfa-2a". New England Journal of Medicine. 330 (2): 88–94. doi:10.1056/NEJM199401133300202. ISSN 0028-4793.
- ↑ Fields, Bernard (2013). Fields virology. Philadelphia: Wolters Kluwer Health/Lippincott Williams & Wilkins. ISBN 9781451105636.