Related Experiment Video
Updated: Feb 9, 2026

"Liver-on-a-Chip" Cultures of Primary Hepatocytes and Kupffer Cells for Hepatitis B Virus Infection
Published on: February 19, 2019
Safety of Direct-Acting Antiviral Therapy Regarding Renal Function in Post-Liver Transplant Patients Infected with
G Peschel1, L Moleda1, L Baier2
1Department of Gastroenterology, Endocrinology, Rheumatology, and Infectious Diseases, University Hospital Regensburg, Regensburg, Germany.
Insights
Direct-acting antiviral (DAA) therapy is safe and effective for liver transplant recipients with hepatitis C virus (HCV). This treatment did not negatively impact renal function, even in patients with pre-existing kidney issues.
Area of Science:
- Hepatology
- Virology
- Nephrology
Background:
- Hepatitis C virus (HCV) infection in liver transplant (LT) recipients can lead to renal or hepatic impairment.
- Direct-acting antivirals (DAA) may interact with immunosuppressants, potentially affecting renal function post-LT.
Purpose of the Study:
- To evaluate the safety and efficacy of DAA therapy in HCV-infected liver transplant patients.
- To assess the impact of DAA therapy on renal function and liver parameters.
Main Methods:
- Single-center study of 18 HCV-infected patients post-LT treated with DAA.
- Primary endpoints: change in glomerular filtration rate (GFR) and sustained virologic response at 12 weeks (SVR12).
- Secondary endpoints: assessment of transaminases, bilirubin, INR, fibrosis, and MELD score.
Main Results:
- All patients achieved SVR12, indicating high efficacy.
- Renal function (GFR) was not significantly affected by DAA therapy, immunosuppression, or pre-existing renal impairment.
- Liver enzymes and bilirubin levels decreased; fibrosis markers improved in some patients.
Conclusions:
- DAA therapy is effective and safe in a real-world cohort of LT recipients with HCV.
- No adverse impact on renal function was observed, even in patients with prior renal impairment.
Background:
Patients after liver transplantation (LT) with hepatitis C virus (HCV) infection often suffer from renal or hepatic impairment. Treating patients after LT with direct-acting antivirals (DAA) might result in decreasing renal function due to interaction of DAA and immunosuppressive therapy. In this single-center study we analyzed clinical parameters of 18 HCV-infected patients treated with DAA therapy after LT.
Methods:
The primary end points were change of renal function (glomerular filtration rate) and sustained virologic response 12 weeks after therapy (SVR12). For secondary end points, we investigated the influence of DAA therapy on transaminases, bilirubin, international normalized ratio, noninvasive fibrosis measurement, and Model for End-Stage Liver Disease (MELD) score.
Results:
Five out of 18 patients treated with DAA suffered from renal impairment stage 2, and 7 patients of renal impairment stage 3. Renal function at SVR12 was not influenced by preexisting renal impairment (P > .5), type of immunosuppressant (P > .5), or type of DAA regimen (P > .5). All patients reached SVR12. The levels of transaminases and bilirubin declined rapidly, as expected. Ten out of 18 patients already suffered from cirrhosis or liver fibrosis >F3 according to noninvasive measurement before initiation of treatment. Single-point acoustic radiation force impulse imaging improved in 9 patients (P = .012). In 7 patients, MELD score improved owing to the decrease of bilirubin levels. In 6 patients it worsened.
Conclusions:
DAA therapy in LT patients was effective and safe in this single-center real-life cohort. Renal function was not influenced by the administered drug combinations, even in patients with preexisting renal impairment.
Related Concept Videos
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Patient-centered Care
Serum Studies: Renal Function Tests
Direct-Acting Cholinergic Agonists: Pharmacokinetics
Sustainable Development
Direct-Acting Cholinergic Agonists: Therapeutic Uses

