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Volume 47, Issue 1, Pages 97-99 (January 2010)


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Resolution of chronic hepatitis Delta after 1 year of combined therapy with pegylated interferon, tenofovir and emtricitabine

Wael Mansourab, Alexandra Ducancelleab, Frédéric Le Galc, Hélène Le Guillou-Guillemetteab, Pierre Abgueguend, Adeline Pivertab, Paul Calèsae, Emmanuel Gordienc, Françoise LunelabCorresponding Author Informationemail address

Received 3 June 2009; received in revised form 22 September 2009; accepted 24 September 2009. published online 16 November 2009.

Abstract 

Background

Hepatitis Delta virus (HDV) Infection has a worldwide distribution, with approximately 20 millions infected persons. Interferon (IFN) is the only approved drug for the treatment of HDV infection which is still a difficult to treat disease.

Objectives

To report a successful treatment of a patient with a chronic severe hepatitis Delta using combination therapy with Pegylated interferon (PegIFN), Tenofovir disoproxil fumarate (TDF) and Emtricitabine (FTC).

Study Design

The patient, a 47 years -old male patient, originating from Dagestan (East Asia), suffered of chronic hepatitis Delta infection. The patient was HBsAg, HBeAg, and anti-Delta Ab (IgG) positive. Serum HBV-DNA level was elevated (more than 9logUI/mL). Serum HDV-RNA level was up to 5.6 log (copies/ml). Genotypes HBV/D and HDV-1 were demonstrated. The liver histology revealed chronic active hepatitis (Metavir score: A2F2).

The treatment was started with PegIFN (180μg/week) for two months and then TDF (300mg/day) (combined later with FTC) was added.

Results

Sustained response was obtained after 10 months of treatment and was accompanied by the clearance of serum hepatitis B virus surface antigen with seroconversion to anti-HBs.

Conclusion

This case report suggests that Delta infection may co-exist with high replicative HBV infection and that combination therapy with PegIFN and nucleoside/tide analogues seems to be more effective than IFN alone. Given that only a single case is reported, further studies including more patients are warranted.

a Laboratoire HIFIH UPRES EA 3859, Faculté de Médecine d’Angers, France

b Laboratoire de virologie, CHU Angers, 4, rue Larrey 49933, Angers cedex 9, France

c Laboratoire de virologie, CH&U Avicenne, associé au CNR des hépatites B, C et Delta, 125, boulevard de Stalingrad 93009 Bobigny cedex, France

d Service des Maladies Infectieuses et Tropicales, CHU, Angers, 4, rue Larrey 49933, Angers cedex 9, France

e Service d’Hépato-Gastroentérologie, CHU, Angers, 4, rue Larrey 49933, Angers cedex 9, France

Corresponding Author InformationCorresponding author at: Laboratory of Virology, Hospital of Angers, 4 rue Larrey, 49933 Angers Cedex 9, France. Tel.: +33 2 41 35 54 93; fax: +33 2 41 35 41 64.

PII: S1386-6532(09)00475-2

doi:10.1016/j.jcv.2009.09.027


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