Mechanism-based drug safety testing using innovative in vitro liver models: from DILI prediction to idiosyncratic DILI liability assessment

Expert Opinion on Drug Metabolism & Toxicology, vol. 21, pp. 769–787

Abstract

Introduction Idiosyncratic drug-induced liver injury (iDILI) remains unpredictable. As adverse responses arise in a small fraction of patients, drugs often fail in later drug development stages or post-approval, thereby tremendously increasing costs and putting patients at risk, highlighting the need for accurate early identification of iDILI liabilities.Covered areas Using articles from the last five years (PubMed), iDILI risk factors are described, in vitro liver models and mechanism-based readout strategies are evaluated on their potential to enable iDILI liability assessment.Expert opinion Various in vitro liver models are established for disease modeling and DILI prediction. Drawbacks for each of these seem inevitable, making the evaluation of their application domain and iDILI liability assessment potential crucial. A tiered approach could be considered, whereby compounds are initially screened and flagged using simple fit-for-purpose models for DILI prediction, followed by multicellular liver models that integrate the current knowledge of iDILI onset in combination with mechanistic readouts. Multiplexing models within an integrated mechanism-based testing strategy could improve the safety assessment accuracy. Defined in vitro models should integrate critical hepatocyte intrinsic risk factors as well as adaptive immune system components to refine iDILI liability assessment.

Authors 4

1. Sibel Bahtiri Aachen Division of Cell Systems and Drug Safety Leiden Academic Centre for Drug Research

   Leiden University

   Affiliation as printed

   Leiden University

   Division of Cell Systems and Drug Safety, Leiden Academic Centre for Drug Research, Leiden University, Leiden, the Netherlands

2. Tessa M. S. Hagens Aachen Division of Cell Systems and Drug Safety Leiden Academic Centre for Drug Research

   Leiden University

   Affiliation as printed

   Leiden University

   Division of Cell Systems and Drug Safety, Leiden Academic Centre for Drug Research, Leiden University, Leiden, the Netherlands

3. Bob van de Water Aachen Division of Cell Systems and Drug Safety Leiden Academic Centre for Drug Research

   Leiden University

   Affiliation as printed

   Leiden University

   Division of Cell Systems and Drug Safety, Leiden Academic Centre for Drug Research, Leiden University, Leiden, the Netherlands

4. Marije Niemeijer corresponding Aachen Division of Cell Systems and Drug Safety Leiden Academic Centre for Drug Research

   Leiden University

   Affiliation as printed

   Leiden University

   Division of Cell Systems and Drug Safety, Leiden Academic Centre for Drug Research, Leiden University, Leiden, the Netherlands