Tohoku J. Exp. Med., 2010, 221(2)
Review
Development of New Anti-tuberculosis Drug Candidates
RUIRU SHI1 and ISAMU SUGAWARA2
1International Tuberculosis Research Department, Henan Provincial Public Health Clinical Center and Henan Provincial Chest Hospital, Henan, China
2 The Research Institute of Tuberculosis, Tokyo, Japan
Mycobacterium tuberculosis, the causative agent of tuberculosis, is a tenacious and remarkably successful pathogen that has latently infected one third of the world's population, according to the World Health Organization (WHO) statistics. It is anticipated that 10% of these infected individuals will develop active tuberculosis at some point in their lifetime. The long-term use of the current drug regimen, the emergence of drug-resistant strains, and HIV co-infection have resulted in a resurgence of research efforts to address the urgent need for new anti-tuberculosis drugs. A number of potential candidate drugs with novel modes of action have entered clinical trials in recent years, and these are likely to be effective against anti-tuberculosis drug-resistant strains. They include neuroquinolone derivatives, a modified ethambutol, nitro-imidazole groups and so on. This mini-review summarizes the latest information about eight new anti-tuberculosis drug candidates and describes their activities, pharmacokinetics, mechanisms of action, and mechanisms of drug-resistance induced by these drug candidates.
keywords —— anti-tuberculosis drug candidates; M. tuberculosis; mechanism of action; multi-drug resistance; XDR-TB
© 2010 Tohoku University Medical Press
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Tohoku J. Exp. Med., 2010, 221, 97-106
Correspondence: Isamu Sugawara, M.D., Ph.D., The Research Institute of Tuberculosis, 3-1-24 Matsuyama, Kiyose, Tokyo 204-0022, Japan.
e-mail: s6671112@sea.plala.or.jp