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Published on: September 25, 2019
[Etanercept and chronic infection by HCV and HBV]
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.
Abstract:
Both psoriasis and chronic infections by HBV and HCV have high prevalence. Thus, it is relatively easy for them to coincide in the same patient. If the psoriasis requires systemic treatment, the dermatologist should consider the hepatic comorbidity when selecting an appropriate treatment. Cyclosporine, in addition to other well-known side effects, is an immunosuppressant that may condition worse evolution of the viral hepatitis. On the other hand, retinoids, psoralens and, above all, methotrexate may worsen the liver function. The anti-TNF-|A biological agents are not hepatotoxic and their theoretical contraindication in this context would be because of their action on the immune response and risk of reactivation of the hepatic infection. However, several studies have demonstrated that neither the viral load nor the hepatic inflammation parameters are generally modified negatively when they are used in hepatitis due to HCV. Their use in this context, with correct monitoring, seems, therefore, very reasonable. On the contrary, in chronic hepatitis B virus, there are cases of worsening, even with fatal outcome in some cases, and the use of these biological agents should be reserved for cases having greater need, and always be associated to antiviral treatment and strict monitoring. The review of the recent literature seems to allow the conclusion that the concomitant use of lamivudine would greatly reduce the risk of viral reactivation and, with this condition, the use of etanercept in some HBV+ patients may also be contemplated.
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