4.2 Review

Development of New Anti-tuberculosis Drug Candidates

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TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE
卷 221, 期 2, 页码 97-106

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TOHOKU UNIV MEDICAL PRESS
DOI: 10.1620/tjem.221.97

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anti-tuberculosis drug candidates; M. tuberculosis; mechanism of action; multi-drug resistance; XDR-TB

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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 ant-ituberculosis drug-resistant strains. They include neuroquinolone derivatives, a modified ethambutol, nitroimidazole 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.

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