GSK2556286 Is a Novel Antitubercular Drug Candidate Effective In Vivo with the Potential To Shorten Tuberculosis Treatment
- PMID: 35607978
- PMCID: PMC9211396
- DOI: 10.1128/aac.00132-22
GSK2556286 Is a Novel Antitubercular Drug Candidate Effective In Vivo with the Potential To Shorten Tuberculosis Treatment
Abstract
As a result of a high-throughput compound screening campaign using Mycobacterium tuberculosis-infected macrophages, a new drug candidate for the treatment of tuberculosis has been identified. GSK2556286 inhibits growth within human macrophages (50% inhibitory concentration [IC50] = 0.07 μM), is active against extracellular bacteria in cholesterol-containing culture medium, and exhibits no cross-resistance with known antitubercular drugs. In addition, it has shown efficacy in different mouse models of tuberculosis (TB) and has an adequate safety profile in two preclinical species. These features indicate a compound with a novel mode of action, although still not fully defined, that is effective against both multidrug-resistant (MDR) or extensively drug-resistant (XDR) and drug-sensitive (DS) M. tuberculosis with the potential to shorten the duration of treatment in novel combination drug regimens. (This study has been registered at ClinicalTrials.gov under identifier NCT04472897).
Keywords: GSK2556286; Mycobacterium tuberculosis; mouse; pharmacology; relapse; tuberculosis.
Conflict of interest statement
The authors declare a conflict of interest. Maria Santos Martínez-Martínez, Jorge Esquivias, Juan Miguel Siles, Marta Alonso, Jaime Escribano, Joaquin Rullas-Trincado, Esther Pérez-Herrán, Gareth Maher-Edwards, Joel Lelievre, Elena Jimenez, Olalla Sanz, Gary Boyle, Sam Turner, Beatriz Urones, Robert H. Bates, David Barros, are employees of GlaxoSmithKline. Eric L. Nuermberger receives research support from Janssen and the TB Alliance.
Figures





References
-
- World Health Organization. 2020. Global tuberculosis report 2020. World Health Organization, Geneva, Switzerland.
-
- Kushner S, Dalalian D, Sanjurjo JL, Bach FL, Jr, Safir SR, Smith VK, Jr, Williams JH. 1952. Experimental chemotherapy of tuberculosis. II. The synthesis of pyrazinamides and related compounds. J Am Chem Soc 74:3617–3621. 10.1021/ja01134a045. - DOI
-
- Malone L, Schurr A, Lindh H, McKenzie D, Kiser JS, Williams JH. 1952. The effect of pyrazinamide (aldinamide) on experimental tuberculosis in mice. Am Rev Tuberc 65:511–518. - PubMed
Publication types
MeSH terms
Substances
Associated data
LinkOut - more resources
Full Text Sources