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.

Frontiers in Medicine
|April 24, 2023
PubMed

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.
Abstract