Center for Discovery and Innovation, and Hackensack Meridian School of Medicine, Department of Medical Sciences, Hackensack Meridian Health, Nutley, NJ, USA.
Harvard T.H. Chan School of Public Health, Department of Immunology and Infectious Diseases, Boston, MA, USA.
Nat Rev Microbiol. 2022 Nov;20(11):685-701. doi: 10.1038/s41579-022-00731-y. Epub 2022 Apr 27.
Despite two decades of intensified research to understand and cure tuberculosis disease, biological uncertainties remain and hamper progress. However, owing to collaborative initiatives including academia, the pharmaceutical industry and non-for-profit organizations, the drug candidate pipeline is promising. This exceptional success comes with the inherent challenge of prioritizing multidrug regimens for clinical trials and revamping trial designs to accelerate regimen development and capitalize on drug discovery breakthroughs. Most wanted are markers of progression from latent infection to active pulmonary disease, markers of drug response and predictors of relapse, in vitro tools to uncover synergies that translate clinically and animal models to reliably assess the treatment shortening potential of new regimens. In this Review, we highlight the benefits and challenges of 'one-size-fits-all' regimens and treatment duration versus individualized therapy based on disease severity and host and pathogen characteristics, considering scientific and operational perspectives.
尽管二十年来,科学界为了理解和治疗结核病而进行了深入研究,但仍然存在生物学上的不确定性,阻碍了进展。然而,由于学术界、制药业和非营利组织等合作倡议,候选药物的研发前景一片光明。这一非凡的成功带来了固有的挑战,即需要为临床试验确定多药方案的优先级,并调整试验设计,以加速方案的开发,并充分利用药物发现方面的突破。目前最需要的是能够预测从潜伏性感染到活动性肺病进展的标志物、药物反应的标志物和复发的预测标志物、能够揭示协同作用的体外工具,这些工具能够在临床上转化,并利用动物模型来可靠地评估新方案的治疗缩短潜力。在这篇综述中,我们从科学和操作的角度出发,强调了“一刀切”方案和基于疾病严重程度以及宿主和病原体特征的个体化治疗的优势和挑战,以及治疗持续时间。