School of Molecular and Cellular Biology and Antimicrobial Research Centre, University of Leeds, Leeds LS2 9JT, UK.
J Antimicrob Chemother. 2013 Mar;68(3):496-505. doi: 10.1093/jac/dks436. Epub 2012 Nov 6.
The discovery and development of antibacterial drugs in the twentieth century were major scientific and medical achievements that have had profound benefits for human society. However, in the twenty-first century the widespread global occurrence of bacteria resistant to the antibiotics and synthetic drugs discovered in the previous century threatens to reverse our ability to treat infectious diseases. Although some new drugs are in development they do not adequately cover growing medical needs. Furthermore, these drugs are mostly derivatives of older classes already in use and therefore prone to existing bacterial resistance mechanisms. Thus, new drug classes are urgently needed. Despite investment in antibacterial drug discovery, no new drug class has been discovered in the past 20 years. In this review, based upon my career as a research scientist in the field of antibacterial drug discovery, I consider some of the technical reasons for the recent failure and look to the future developments that may help to reverse the poor current success rate. Diversification of screening libraries to include new natural products will be important as well as ensuring that the promising drug hits arising from structure-based drug design can achieve effective concentrations at their target sites within the bacterial cell.
在二十世纪,抗菌药物的发现和开发是重大的科学和医学成就,为人类社会带来了深远的益处。然而,在二十一世纪,上世纪发现的抗生素和合成药物在全球范围内广泛出现耐药菌,这有可能使我们治疗传染病的能力发生逆转。尽管正在开发一些新药,但它们并不能充分满足不断增长的医疗需求。此外,这些药物大多是已有药物类别的衍生物,因此容易产生现有的细菌耐药机制。因此,迫切需要新的药物类别。尽管在抗菌药物发现方面进行了投资,但在过去 20 年中没有发现新的药物类别。在这篇综述中,基于我作为抗菌药物发现领域的研究科学家的职业生涯,我考虑了近期失败的一些技术原因,并展望了未来的发展,这些发展可能有助于扭转目前成功率低的局面。多样化的筛选库,包括新的天然产物,以及确保基于结构的药物设计产生的有前途的药物命中能够在细菌细胞内达到其靶位的有效浓度,都将是重要的。