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Updated: Apr 4, 2026

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
Published on: January 31, 2022
Liver toxicity associated with sofosbuvir, an NS5A inhibitor and ribavirin use
Jessica K Dyson1, John Hutchinson2, Laura Harrison2
1Liver Unit, Freeman Hospital, Newcastle upon Tyne, UK; Institute of Cellular Medicine, Newcastle University, UK.
Abstract:
Hepatitis C virus (HCV) infection is a major cause of end-stage liver disease and hepatocellular carcinoma. There have been rapid advances in HCV treatment with the development of oral direct-acting antivirals (DAAs). Studies have shown sustained virological response rates above 90% with combinations of DAAs, including patients with compensated cirrhosis. Thus far, significant drug toxicity has not been seen with these agents, but there is limited experience of using DAAs in decompensated HCV cirrhosis. This report describes the first experience of serious drug-induced hepatotoxicity with the new DAAs. The mechanism underlying these drug reactions is currently unknown. Few patients with decompensated cirrhosis have been treated with DAAs, so the exact pharmacokinetics in this population have not been characterised. In both cases presented here, patients were taking or had recently taken other drugs. It is possible that an unknown interaction or reaction to the drug combination caused the hepatotoxicity. Although the association with the DAAs is not proven these cases indicate that patients with advanced liver disease need close monitoring while on DAA therapy and if there is a significant unexplained deterioration in liver function the DAAs should be discontinued.
Insights
Hepatitis C virus (HCV) direct-acting antivirals (DAAs) show high efficacy but can cause serious liver injury in decompensated cirrhosis. Close monitoring is crucial for advanced liver disease patients on DAA therapy.
Area of Science:
- Hepatology
- Virology
- Pharmacology
Background:
- Hepatitis C virus (HCV) infection leads to severe liver disease.
- Oral direct-acting antivirals (DAAs) have revolutionized HCV treatment, achieving high sustained virological response rates.
- Existing data primarily includes patients with compensated cirrhosis.
Observation:
- Limited experience exists with DAAs in patients who have decompensated HCV cirrhosis.
- This report details the first observed cases of severe drug-induced hepatotoxicity linked to new DAAs in this population.
- Potential drug interactions or unknown reactions are suspected mechanisms, as patients were on other medications.
Findings:
- The exact pharmacokinetics of DAAs in decompensated cirrhosis are not well-characterized.
- Two cases of serious hepatotoxicity associated with DAA use in decompensated cirrhosis are presented.
- The underlying mechanism of these drug reactions remains unknown.
Implications:
- Patients with advanced liver disease require vigilant monitoring during DAA therapy.
- Discontinuation of DAAs is recommended if significant, unexplained liver function deterioration occurs.
- Further research is needed to understand DAA safety and pharmacokinetics in decompensated cirrhosis.
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