New tuberculosis drug targets, their inhibitors, and potential therapeutic impact

Transl Res. 2020 Jun:220:68-97. doi: 10.1016/j.trsl.2020.03.007. Epub 2020 Mar 16.

Abstract

The current tuberculosis (TB) predicament poses numerous challenges and therefore every incremental scientific work and all positive socio-political engagements, are steps taken in the right direction to eradicate TB. Progression of the late stage TB-drug pipeline into the clinics is an immediate deliverable of this global effort. At the same time, fueling basic research and pursuing early discovery work must be sustained to maintain a healthy TB-drug pipeline. This review encompasses a broad analysis of chemotherapeutic strategies that target the DNA replication, protein synthesis, cell wall biosynthesis, energy metabolism and proteolysis of Mycobacterium tuberculosis (Mtb). It includes a status check of the current TB-drug pipeline with a focus on the associated biology, emerging targets, and their promising chemical inhibitors. Potential synergies and/or gaps within or across different chemotherapeutic strategies are systematically reviewed as well.

Publication types

  • Review

MeSH terms

  • Antitubercular Agents / pharmacology*
  • Antitubercular Agents / therapeutic use
  • Cell Wall / drug effects
  • Cell Wall / metabolism
  • DNA Replication / drug effects
  • Energy Metabolism / drug effects
  • Mycolic Acids / antagonists & inhibitors
  • Protein Synthesis Inhibitors / pharmacology
  • Proteolysis / drug effects

Substances

  • Antitubercular Agents
  • Mycolic Acids
  • Protein Synthesis Inhibitors