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Published on: September 25, 2019
Hepatitis B virus reactivation during immunosuppressive therapy: Appropriate risk stratification
1Wai-Kay Seto, Department of Medicine, the University of Hong Kong, Queen Mary Hospital, Hong Kong, China.
Hepatitis B virus (HBV) reactivation risk during immunosuppressive therapy is significant for both HBsAg-positive and HBsAg-negative individuals. Prophylactic antiviral therapy, particularly entecavir, is effective in preventing HBV reactivation in HBsAg-positive patients.
Area of Science:
- Hepatology
- Immunology
- Virology
Background:
- Hepatitis B virus (HBV) reactivation is a concern during immunosuppressive therapy.
- Reactivation occurs in hepatitis B surface antigen (HBsAg)-positive and HBsAg-negative, anti-HBc-positive individuals.
- Specific immunosuppressive agents like rituximab and anti-TNF increase reactivation risk.
Purpose of the Study:
- To review current understanding of HBV reactivation during immunosuppression.
- To compare antiviral prophylaxis efficacy.
- To highlight the need for risk stratification in managing HBV reactivation.
Main Methods:
- Literature review of HBV reactivation during immunosuppressive therapy.
- Analysis of data on prophylactic antiviral efficacy.
- Evaluation of reactivation risks in different patient groups and therapies.
Main Results:
- Prophylactic antiviral therapy effectively prevents HBV reactivation in HBsAg-positive patients.
- Entecavir shows greater efficacy than lamivudine for prophylaxis.
- HBsAg-negative, anti-HBc-positive individuals have varying reactivation risks depending on immunosuppression type, with rituximab showing a 41.5% 2-year cumulative risk.
Conclusions:
- Optimal management requires risk stratification for both HBsAg-positive and HBsAg-negative, anti-HBc-positive individuals.
- Further prospective data is needed for certain immunosuppressive regimens in HBsAg-negative patients.
- Tailored strategies are essential to prevent HBV reactivation effectively.
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