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Updated: Aug 1, 2025

Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 23, 2014
Distinct histological patterns in chronic hepatitis D with nucleos(t)ide analogue therapy
Julian Hercun1, Theo Heller1, Jeffrey S Glenn2
1Translational Hepatology Section, Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, United States.
Nucleos(t)ide analog therapy in chronic hepatitis delta virus (HDV) infection is linked to a distinct membranous hepatitis B surface antigen staining pattern. This unique histological finding in HDV patients on treatment does not correlate with viral activity.
Area of Science:
- Hepatology
- Virology
- Pathology
Background:
- Chronic hepatitis delta virus (HDV) infection causes more severe liver disease than hepatitis B virus (HBV) alone.
- Histological staining patterns in HBV mono-infection are known, but less studied in HDV co-infection.
- The impact of nucleos(t)ide analog (NA) therapy on HBV in HDV co-infection requires further investigation.
Purpose of the Study:
- To evaluate the effect of nucleos(t)ide analog (NA) therapy for concurrent hepatitis B virus (HBV) infection on the histological appearance of chronic hepatitis delta virus (HDV).
Main Methods:
- Retrospective review of liver biopsies from patients with HDV infection.
- Evaluation of hepatitis-specific stains for HBV antigens.
- Comparison of clinical and histological features between patients on and off NA therapy.
Main Results:
- Fifty patients were analyzed; 26 (52%) were on NA therapy.
- Patients on NA therapy showed a significantly higher odds ratio for membranous staining (7.15) compared to those off NA therapy (0.13).
- Membranous staining was associated with lower total inflammation scores, but not with markers of disease severity or viral activity.
Conclusions:
- Nucleos(t)ide analog treatment in chronic HDV infection is associated with a unique membranous hepatitis B surface antigen staining pattern.
- This histological pattern is independent of HBV or HDV replicative activity.
- Findings enhance understanding of HBV-directed therapy's role in HDV pathophysiology.
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