Development and analysis of an in vitro model of inflammatory cytokine-mediated idiosyncratic drug hepatotoxicity

Idiosyncratic drug reactions are a subset of adverse reactions frequently targeting the liver, which become obvious only in large sample populations. Drug-induced hepatotoxicity, occurring in a very small fraction of patients, poses a major challenge to pharmaceutical companies due to its unknown mechanism(s) of action and deficient models for study. In vitro model systems may have the potential to predict this liver injury by generating conditions possibly representing key processes involved, both directly and indirectly, in drug effects on cellular physiology. Our ultimate goal is to develop an in vitro model effectively mimicking certain relevant aspects of the in vivo response of the human liver. In our initial effort described herein, we have designed a novel cell-based system using alternatively in both a human hepatoma cell line and primary rat hepatocytes to study toxic effects in a background reflecting in vivo inflammatory conditions. This background incorporates bacterial lipopolysaccharide (LPS) administration along with inflammatory cytokines (tumor necrosis factor, interferon y, interleukin-1 a, interleukin-113, and interleukin-6) previously shown to increase in LPS-administrated rats. Our study began with an investigation of toxicities that are induced by combinations of five cytokines and LPS in HepG2 and C3A human hepatoma cell lines and in primary rat hepatocytes. Informed by the results of these experiments, we selected representative cytokine/LPS treatments and cell systems to examine drug-cytokine synergies in vitro and were able to identify multiple idiosyncratic hepatotoxins that induced synergistic toxicity in either the HepG2 cell line or primary rat hepatocytes.

Department dc:contributor.department

Massachusetts Institute of Technology. Biological Engineering Division.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2007

Author dc:creator

• Hasan, Maya

Advisor dc:contributor.advisor

• Douglas A. Lauffenburger.

• Biological Engineering Division.

Statement dc:rights

• MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/42387

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/42387