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内外抑制结核分枝杆菌。

Inhibiting Mycobacterium tuberculosis within and without.

作者信息

Cole Stewart T

机构信息

Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, Station 19, 1015 Lausanne, Switzerland

出版信息

Philos Trans R Soc Lond B Biol Sci. 2016 Nov 5;371(1707). doi: 10.1098/rstb.2015.0506.

Abstract

Tuberculosis remains a scourge of global health with shrinking treatment options due to the spread of drug-resistant strains of Mycobacterium tuberculosis Intensive efforts have been made in the past 15 years to find leads for drug development so that better, more potent drugs inhibiting new targets could be produced and thus shorten treatment duration. Initial attempts focused on repurposing drugs that had been developed for other therapeutic areas but these agents did not meet their goals in clinical trials. Attempts to find new lead compounds employing target-based screens were unsuccessful as the leads were inactive against M. tuberculosis Greater success was achieved using phenotypic screening against live tubercle bacilli and this gave rise to the drugs bedaquiline, pretomanid and delamanid, currently in phase III trials. Subsequent phenotypic screens also uncovered new leads and targets but several of these targets proved to be promiscuous and inhibited by a variety of seemingly unrelated pharmacophores. This setback sparked an interest in alternative screening approaches that mimic the disease state more accurately. Foremost among these were cell-based screens, often involving macrophages, as these should reflect the bacterium's niche in the host more faithfully. A major advantage of this approach is its ability to uncover functions that are central to infection but not necessarily required for growth in vitro For instance, inhibition of virulence functions mediated by the ESX-1 secretion system severely attenuates intracellular M. tuberculosis, preventing intercellular spread and ultimately limiting tissue damage. Cell-based screens have highlighted the druggability of energy production via the electron transport chain and cholesterol metabolism. Here, I review the scientific progress and the pipeline, but warn against over-optimism due to the lack of industrial commitment for tuberculosis drug development and other socio-economic factors.This article is part of the themed issue 'The new bacteriology'.

摘要

结核病仍然是全球健康的一大祸害,由于耐药结核分枝杆菌菌株的传播,治疗选择日益减少。在过去15年里,人们付出了巨大努力来寻找药物开发的线索,以便能够生产出更好、更有效的抑制新靶点的药物,从而缩短治疗时间。最初的尝试集中在重新利用为其他治疗领域开发的药物,但这些药物在临床试验中未能达到目标。利用基于靶点的筛选方法寻找新的先导化合物的尝试也未成功,因为这些先导化合物对结核分枝杆菌没有活性。使用针对活结核杆菌的表型筛选取得了更大的成功,这催生了目前处于III期试验的药物贝达喹啉、普瑞玛尼和地拉马尼。随后的表型筛选也发现了新的先导化合物和靶点,但其中一些靶点被证明具有多效性,会受到各种看似无关的药效基团的抑制。这一挫折引发了人们对更准确模拟疾病状态的替代筛选方法的兴趣。其中最重要的是基于细胞的筛选,通常涉及巨噬细胞,因为这些细胞应该更忠实地反映细菌在宿主中的生态位。这种方法的一个主要优点是它能够发现对感染至关重要但不一定是体外生长所必需的功能。例如,抑制由ESX-1分泌系统介导的毒力功能会严重减弱细胞内结核分枝杆菌,防止细胞间传播并最终限制组织损伤。基于细胞的筛选突出了通过电子传递链产生能量和胆固醇代谢的可药用性。在此,我回顾了科学进展和研发流程,但也警告不要因缺乏结核病药物开发的产业投入和其他社会经济因素而过度乐观。本文是主题为“新细菌学”的特刊的一部分。

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