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Mechanisms of drug-induced liver injury

Stephens, Camilla; Andrade, Raúl J.; Lucena, M. Isabel

Current Opinion in Allergy & Clinical Immunology: August 2014 - Volume 14 - Issue 4 - p 286–292
doi: 10.1097/ACI.0000000000000070
DRUG ALLERGY: Edited by Bernard Y. Thong and Miguel Blanca

Purpose of review: Idiosyncratic drug-induced liver injury (iDILI) is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical industry. Despite increased awareness of iDILI, its underlying mechanism is still not fully understood. This review summarizes the current understanding of the molecular mechanism behind iDILI.

Recent findings: Genetic variations in drug metabolizing genes are in line with proposed mechanisms based on acetaminophen hepatotoxicity, whereby reactive metabolites covalently bind to cellular proteins and disturb the redox balance. In addition, immune-mediated effects have been reported for flucloxacillin hepatotoxicity, demonstrating both haptenization and direct binding between the drug and immune receptors.

Summary: Idiosyncratic DILI development is believed to be orchestrated by multiple events, such as reactive metabolite formations, oxidative stress and signalling pathway inductions, with the mitochondria taking centre stage. Evidence also points towards the immune system (innate and adaptive responses) as important components in iDILI. Interindividual differences in one or more of these events, due to genetic variations and environmental factors, are likely to contribute to the idiosyncratic nature of this condition and subsequently distinguish between patient susceptibility and tolerance.

Servicio de Farmacología Clínica and UGC de Gastroenterología y Hepatología, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Málaga and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd) Madrid, Spain

Correspondence to M. Isabel Lucena, MD, PhD, Departamento de Farmacología, Facultad de Medicina, Boulevard Louis Pasteur 32, 29071 Málaga, Spain. Tel: +34 952 131572; fax: +34 952 131568; e-mail: lucena@uma.es

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