Distinct histological patterns in chronic hepatitis D with nucleos(t)ide analogue therapy
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Updated: Aug 1, 2025

Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 23, 2014
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.
Insights
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.
Background:
Chronic hepatitis delta virus (HDV) infection leads to a more severe hepatitis than hepatitis B virus (HBV) infection alone. Specific histological staining patterns have been described in HBV mono-infection, however this has not been extensively investigated in HDV co-infection. This study evaluated whether the use of nucleos(t)ide analogs (NAs) for concurrent HBV infection has an impact on the histological appearance of chronic HDV.
Methods:
Liver biopsies of all patients referred for management of HDV infection were reviewed and hepatitis-specific stains for HBV antigens were evaluated. Clinical and histological characteristics were compared between patients on and off-NA therapy.
Results:
50 patients were included in our analysis, of which 26 (52%) were on NA therapy at the time of the biopsy. Overall, 8% stained for HBV core antigen and 86% stained for HBV surface antigen. On and off-NA groups had similar degrees of fibrosis and inflammation, however NA patients had an odds ratio of 7.15 for membranous staining and 0.13 for scattered granular staining (p = 0.001). No association was found with markers of disease severity or viral activity, with nonetheless a lower score of total inflammation noted in biopsies with a positive membranous stain (8.5 vs. 10.3 p = 0.04).
Conclusion:
In chronic HDV infection, patients treated with nucleos(t)ide analogs demonstrate a unique membranous staining pattern for hepatitis B surface antigen, which is not associated with HBV or HDV replicative activity. These findings may help improve the understanding of the role of HBV directed therapy in HDV pathophysiology.
Highlights:
Histological staining is associated with viral activity in chronic HBV, however this has been infrequently explored in HDV. In HDV, staining patterns differ based on HBV treatment status and do not appear to be associated with markers of viral activity.
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