Gatifloxacin and ethionamide as the foundation for therapy of tuberculosis

Antimicrob Agents Chemother. 2003 Aug;47(8):2442-4. doi: 10.1128/AAC.47.8.2442-2444.2003.

Abstract

The use of gatifloxacin (GAT) in combination with ethionamide (ETA) with or without pyrazinamide (PZA) for a 12-week treatment period followed by an 8-week observation period was evaluated in a model of tuberculosis in mice. Mice treated with GAT at 300 mg/kg of body weight in combination with ETA (25 mg/kg) for 5 days per week had sterile lungs, whereas mice treated with GAT (100 mg/kg) and ETA (25 mg/kg) had about 10 CFU/lung; however, there was regrowth of the organisms in both groups at the end of the observation period. When PZA (450 mg/kg 5 days per week) was added to the high-dose GAT-ETA regimen, no viable mycobacteria were present after the 8-week observation period. GAT in combination with ETA and PZA has great promise for the treatment of tuberculosis.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Administration, Intranasal
  • Animals
  • Anti-Infective Agents / therapeutic use*
  • Antitubercular Agents / therapeutic use*
  • Colony-Forming Units Assay
  • Dose-Response Relationship, Drug
  • Drug Resistance, Multiple, Bacterial
  • Ethionamide / therapeutic use*
  • Female
  • Fluoroquinolones*
  • Gatifloxacin
  • Lung / microbiology
  • Mice
  • Mice, Inbred C57BL
  • Mycobacterium tuberculosis / drug effects
  • Tuberculosis / drug therapy*
  • Tuberculosis / microbiology

Substances

  • Anti-Infective Agents
  • Antitubercular Agents
  • Fluoroquinolones
  • Gatifloxacin
  • Ethionamide