[Etanercept and chronic infection by HCV and HBV]

X Bordas1, S Martín-Sala

  • 1Servicio de Dermatología, Hospital de Bellvitge, Barcelona, España. xbordas@bellvitgehospital.cat

Insights

Psoriasis patients with chronic hepatitis B or C require careful systemic treatment selection. Anti-TNF-alpha agents are generally safe for HCV, but require caution and antiviral therapy for HBV to prevent worsening.

Area of Science:

  • Hepatology
  • Dermatology
  • Immunology

Background:

  • Psoriasis and viral hepatitis (Hepatitis B Virus [HBV] and Hepatitis C Virus [HCV]) are prevalent conditions.
  • Co-occurrence in patients necessitates careful consideration of systemic psoriasis treatments due to potential hepatic comorbidities.

Observation:

  • Traditional systemic treatments like cyclosporine, retinoids, psoralens, and methotrexate can negatively impact liver function or viral hepatitis progression.
  • Anti-tumor necrosis factor-alpha (anti-TNF-α) biological agents are not directly hepatotoxic, but pose a theoretical risk of immune modulation and viral reactivation.

Findings:

  • Studies indicate anti-TNF-α agents do not generally worsen viral load or hepatic inflammation in HCV patients, suggesting safe use with monitoring.
  • In contrast, HBV cases show potential for worsening, even fatal outcomes, with anti-TNF-α use, necessitating strict monitoring and antiviral co-therapy.
  • Lamivudine combined with etanercept may be a viable option for select HBV+ patients, significantly reducing viral reactivation risk.

Implications:

  • Dermatologists must weigh the risks and benefits of systemic psoriasis treatments in patients with viral hepatitis.
  • Anti-TNF-α agents appear to be a reasonable option for psoriasis patients with HCV under appropriate monitoring.
  • Careful patient selection, antiviral prophylaxis (e.g., lamivudine), and rigorous monitoring are crucial for using anti-TNF-α agents in psoriasis patients with HBV.

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