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Tuberculosis: Pathogenesis, Current Treatment Regimens and New Drug Targets

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MDPI
DOI: 10.3390/ijms24065202

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tuberculosis; TB pathogenesis; latent TB; TB treatment regimens; mycobacterial drug targets; anti-TB drug candidates

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Mycobacterium tuberculosis (M. tb) is a highly prevalent pathogen causing tuberculosis (TB), which affects a quarter of the global population in latent form and becomes active under immunocompromised conditions. TB treatment requires a 6-month protocol with four drugs, but non-compliance and poverty have led to the emergence of drug-resistant strains requiring longer and more toxic treatment. Only three new drugs have been approved in the last decade, reflecting the challenges in developing novel anti-TB drugs. This review discusses M. tb pathogenesis, current treatment protocols, and promising new drug candidates.
Mycobacterium tuberculosis (M. tb), the causative agent of TB, is a recalcitrant pathogen that is rife around the world, latently infecting approximately a quarter of the worldwide population. The asymptomatic status of the dormant bacteria escalates to the transmissible, active form when the host's immune system becomes debilitated. The current front-line treatment regimen for drug-sensitive (DS) M. tb strains is a 6-month protocol involving four different drugs that requires stringent adherence to avoid relapse and resistance. Poverty, difficulty to access proper treatment, and lack of patient compliance contributed to the emergence of more sinister drug-resistant (DR) strains, which demand a longer duration of treatment with more toxic and more expensive drugs compared to the first-line regimen. Only three new drugs, bedaquiline (BDQ) and the two nitroimidazole derivatives delamanid (DLM) and pretomanid (PMD) were approved in the last decade for treatment of TB-the first anti-TB drugs with novel mode of actions to be introduced to the market in more than 50 years-reflecting the attrition rates in the development and approval of new anti-TB drugs. Herein, we will discuss the M. tb pathogenesis, current treatment protocols and challenges to the TB control efforts. This review also aims to highlight several small molecules that have recently been identified as promising preclinical and clinical anti-TB drug candidates that inhibit new protein targets in M. tb.

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