Williams Kerstin J, Duncan Ken
Centre for Molecular Microbiology and Infection, 3.40 Flowers Building, Imperial College, South Kensington, London SW1 2AZ, UK.
Curr Mol Med. 2007 May;7(3):297-307. doi: 10.2174/156652407780598575.
There is an urgent need for new drugs to treat tuberculosis. During the last forty years the only drugs to have been developed are variations on existing ones, but new drug candidates must offer improvements over existing agents. In particular, we require new drugs having novel mechanisms of action that are active against drug-resistant strains and also kill persistent bacilli, thus shortening the length of chemotherapy. Recent advances in our understanding of the biology of Mycobacterium tuberculosis, in particularly the availability of the genome sequence coupled with development of new genetic tools, have greatly contributed to the discovery of potential drug targets for new antituberculars. However, although many potential new drug targets have been identified, greater effort is required in target validation to show properly that they are essential for bacterial growth and survival. In this review, the current drug development pipeline and the strategies employed to identify and validate novel tuberculosis drug targets are presented.
迫切需要新的药物来治疗结核病。在过去的四十年里,唯一研发出的药物都是现有药物的变体,但新的候选药物必须比现有药物有所改进。特别是,我们需要具有新作用机制的新药,这些新药要对耐药菌株有活性,还要能杀死持续存在的杆菌,从而缩短化疗疗程。我们对结核分枝杆菌生物学的理解取得了最新进展,尤其是基因组序列的可得性以及新遗传工具的开发,这极大地促进了新型抗结核药物潜在靶点的发现。然而,尽管已经确定了许多潜在的新药物靶点,但在靶点验证方面仍需要付出更大努力,以充分证明它们对细菌生长和存活至关重要。在这篇综述中,介绍了当前的药物研发流程以及用于识别和验证新型结核病药物靶点的策略。