The role of cytokines and chemokines in the development of steatohepatitis.

Patricia Lalor, Jeffrey Faint, Y Aarbodem, Stefan Hubscher, David Adams

Research output: Contribution to journalArticle

92 Citations (Scopus)

Abstract

Nonalcoholic fatty liver disease (NAFLD) and alcoholic liver disease (ALD) share similar morphological characteristics despite the obvious etiological differences between the two conditions. In both conditions the first manifestation of injury is the accumulation of fat within hepatocytes (steatosis), and in a proportion of patients this is followed by the development of necroinflammatory activity that leads to cirrhosis. Steatosis alone is considered to be relatively innocuous and is usually reversible, and it is the development of liver cell ballooning and inflammation (steatohepatitis) that determines whether a patient progresses to irreversible liver damage and fibrosis. This has led to the two-hit theory in which the first hit is accumulation of fat in the liver and the second hit involves an inflammatory insult or challenge to the liver, for example, through oxidative stress or in response to pathogenic stimuli such as endotoxin. Although the nature of the hits remains poorly understood, it is clear that the critical event in progression is the development of inflammation, and the fact that it is impossible to distinguish alcoholic from nonalcoholic steatohepatitis on histological grounds suggests that common pathogenic mechanisms are involved. We focus on the role of cytokines and particularly chemokines in instigating and driving the inflammatory infiltrate in steatohepatitis. A better understanding of this process might allow therapeutic intervention to switch off the inflammatory response before irreversible damage occurs in both ALD and NAFLD.
Original languageEnglish
Pages (from-to)173-93
Number of pages21
JournalSeminars in Liver Disease
Volume27
Issue number2
DOIs
Publication statusPublished - 1 May 2007

Keywords

  • ethanol
  • inflammation
  • endotholium
  • adhesion molecules
  • chemokines
  • steatohepatitis

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