Management of Patients with Hepatitis B Core Antibodies
Patients with positive hepatitis B core antibodies (anti-HBc) require risk assessment and monitoring for potential HBV reactivation, particularly before immunosuppressive therapy. 1
Understanding Anti-HBc Status
Hepatitis B core antibody (anti-HBc) indicates previous exposure to HBV. There are several possible clinical scenarios:
Isolated anti-HBc positive: When anti-HBc is positive but HBsAg and anti-HBs are negative
- May represent resolved infection with waning anti-HBs
- May indicate occult HBV infection (low-level HBV DNA present)
- May rarely be a false-positive result 2
Anti-HBc and anti-HBs positive: Indicates resolved past infection with immunity 1
- Distinguished from vaccine-induced immunity (which would show positive anti-HBs but negative anti-HBc)
Initial Assessment
For patients with positive anti-HBc, the following tests should be performed:
- HBsAg to rule out chronic infection
- Anti-HBs to assess for immunity
- HBV DNA to detect occult infection
- Liver function tests (ALT, AST)
- Assessment for other viral hepatitis (HCV, HDV if indicated) 2
Management Based on Serological Pattern
1. Resolved HBV Infection (HBsAg negative, anti-HBc positive, anti-HBs positive)
- No specific antiviral treatment needed
- No routine monitoring of HBV DNA required in immunocompetent patients
- Patient education about potential reactivation with immunosuppression 1
2. Isolated Anti-HBc (HBsAg negative, anti-HBc positive, anti-HBs negative)
- Consider HBV DNA testing to rule out occult infection
- Consider hepatitis B vaccination to induce anti-HBs response
- Monitor for potential reactivation if immunosuppression is planned 2
3. Chronic HBV Infection (HBsAg positive, anti-HBc positive)
- Refer to specialist for comprehensive evaluation
- Further assessment with HBeAg, anti-HBe, HBV DNA, liver function tests
- Consider antiviral therapy based on disease activity 2
Risk Assessment for HBV Reactivation
The risk of HBV reactivation in patients with positive anti-HBc varies based on:
Immunosuppression regimen:
- High risk (>10%): B-cell depleting agents (e.g., rituximab), stem cell transplantation
- Moderate risk (1-10%): TNF-α inhibitors, high-dose corticosteroids, cytotoxic chemotherapy
- Low risk (<1%): Traditional immunosuppressants, low-dose corticosteroids 1
HBsAg status:
- HBsAg-positive patients have higher reactivation risk
- Anti-HBc positive/HBsAg-negative patients still have significant risk with certain immunosuppressants 2
Management During Immunosuppressive Therapy
For patients requiring immunosuppressive therapy:
High-risk immunosuppression:
- Prophylactic antiviral therapy (entecavir or tenofovir) during and for 12 months after therapy
- Monitor HBsAg and ALT during treatment 2
Moderate-risk immunosuppression:
Low-risk immunosuppression:
- Monitor ALT every 3 months
- Test for HBsAg if ALT elevates 1
Antiviral Options
If antiviral therapy is indicated:
- Preferred agents: Entecavir (0.5 mg daily) or tenofovir (300 mg daily) due to high barrier to resistance 3, 4
- Duration: Continue for at least 6-12 months after discontinuation of immunosuppressive therapy 2
- Monitoring: Regular assessment of renal function, especially with tenofovir 4
Patient Education and Follow-up
- Inform patients they have evidence of past HBV infection
- Explain the risk of reactivation with immunosuppression
- Advise patients to inform all healthcare providers about their HBV status
- Recommend hepatitis A vaccination if not immune 1
- Counsel on avoiding alcohol and hepatotoxic substances 1
Common Pitfalls to Avoid
- Misinterpreting isolated anti-HBc as a false positive without considering occult HBV
- Failing to screen for HBV before starting immunosuppressive therapy
- Using lamivudine for prophylaxis instead of high-barrier-to-resistance antivirals
- Discontinuing antiviral prophylaxis too early after immunosuppressive therapy
- Not monitoring patients on immunosuppression who have evidence of past HBV infection
By following this approach, clinicians can effectively manage patients with hepatitis B core antibodies and minimize the risk of HBV reactivation, particularly in the context of immunosuppressive therapy.