Tumor necrosis factor- alpha promoter polymorphism at position -308 predicts response to combination therapy in hepatitis C virus infection

J Infect Dis. 2006 Jan 1;193(1):98-101. doi: 10.1086/498244. Epub 2005 Nov 16.

Abstract

The G-->A transition in the tumor necrosis factor (TNF)- alpha promoter region at position -308 (TNF308.2) and -238 (TNF238.2) were determined in 141 patients with chronic hepatitis C virus (HCV) infection. Patients received combination therapy with high-dose interferon (IFN)- alpha and ribavirin for 24 weeks. A total of 100 patients (70.9%) had a sustained virologic response (SVR) after treatment. The TNF308.2 allele was independently associated with an SVR, particularly in patients with HCV genotype 1b infection and >200,000 IU of HCV RNA/mL in serum. In conclusion, the response to combination therapy with high-dose IFN- alpha and ribavirin may be associated, at least in part, with host genetic factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antiviral Agents / therapeutic use
  • Drug Therapy, Combination
  • Female
  • Hepacivirus
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / virology
  • Humans
  • Interferon-alpha / therapeutic use
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Predictive Value of Tests
  • Promoter Regions, Genetic / genetics*
  • Ribavirin / therapeutic use
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / genetics*

Substances

  • Antiviral Agents
  • Interferon-alpha
  • Tumor Necrosis Factor-alpha
  • Ribavirin