Unbound MEDLINE

Addition of PNU-100480 to First-line Drugs Shortens the Time Needed to Cure Murine Tuberculosis. American journal of respiratory and critical care medicine [Am J Respir Crit Care Med] Journal article

 
TitleAddition of PNU-100480 to First-line Drugs Shortens the Time Needed to Cure Murine Tuberculosis.
Author(s)Williams KN, Brickner SJ, Stover CK, Zhu T, Ogden A, Tasneen R, Tyagi S, Grosset JH, Nuermberger EL 
InstitutionCenter for Tuberculosis Research, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
SourceAm J Respir Crit Care Med 2009 Jun 11.
AbstractRATIONALE: We recently reported strong bactericidal activity of the oxazolidinone PNU-100480 and its ability to increase the initial bactericidal effect of various combinations of first-line tuberculosis drugs and moxifloxacin in a murine model. Objectives and
METHODS: Therefore, we investigated whether the addition of PNU-100480 to the standard first-line regimen of rifampin, isoniazid and pyrazinamide could shorten the duration of treatment necessary to prevent relapse after treatment discontinuation.
MEASUREMENTS AND MAIN RESULTS: After 2 months of treatment mice receiving PNU-100480 in addition to the first-line regimen had lung CFU counts 2 orders of magnitude lower than control mice receiving the first-line regimen alone. Relapse rates after 4 months of treatment were 90%, 35% and 5% when PNU-100480 was added to the first-line regimen for 0, 2 and 4 months, respectively. When the total treatment duration was 3 months, relapse rates were 85% and 35-45% when mice received PNU-100480 for 2 and 3 months, respectively; all control mice remained culture positive at the time of treatment completion with 17-72 CFU per lung. Addition of linezolid to the first-line regimen had an antagonistic effect resulting in higher CFU counts and failure to render mice culture-negative in 4 months of treatment.
CONCLUSIONS: Together with previous findings, these results confirm that PNU-100480, which is now in Phase I clinical testing, has sterilizing activity in the murine model and suggest that it may be capable of shortening treatment duration for drug-susceptible as well as drug-resistant tuberculosis in humans.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19520903
  
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