SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology and Institute of Infectious Disease & Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
Division of Clinical Pharmacology, Department of Medicine, Faculty of Health Sciences, University of Cape Town, Observatory, South Africa.
IUBMB Life. 2018 Sep;70(9):926-937. doi: 10.1002/iub.1866. Epub 2018 Jun 22.
Anti-tuberculosis (TB) drugs possess diverse abilities to penetrate the different host tissues and cell types in which infecting Mycobacterium tuberculosis bacilli are located during active disease. This is important since there is increasing evidence that the respective "lesion-penetrating" properties of the front-line TB drugs appear to correlate well with their specific activity in standard combination therapy. In turn, these observations suggest that rational efforts to discover novel treatment-shortening drugs and drug combinations should incorporate knowledge about the comparative abilities of both existing and experimental anti-TB agents to access bacilli in defined physiological states at different sites of infection, as well as avoid elimination by efflux or inactivation by host or bacterial metabolism. However, while there is a fundamental requirement to understand the mode of action and pharmacological properties of any current or experimental anti-TB agent within the context of the obligate human host, this is complex and, until recently, has been severely limited by the available methodologies and models. Here, we discuss advances in analytical models and technologies which have enabled investigations of drug metabolism and pharmacokinetics (DMPK) for new TB drug development. In particular, we consider the potential to shift the focus of traditional pharmacokinetic-pharmacodynamic analyses away from plasma to a more specific "site of action" drug exposure as an essential criterion for drug development and the design of dosing strategies. Moreover, in summarising approaches to determine DMPK data for the "unit of infection" comprising host macrophage and intracellular bacillus, we evaluate the potential benefits of including these analyses at an early stage in the preclinical drug development algorithm. © 2018 IUBMB Life, 70(9):926-937, 2018.
抗结核(TB)药物具有多种能力,可穿透活动性疾病中感染结核分枝杆菌的不同宿主组织和细胞类型。这一点很重要,因为越来越多的证据表明,一线抗结核药物各自的“穿透病变”特性似乎与其在标准联合治疗中的特定活性密切相关。反过来,这些观察结果表明,为发现新的缩短治疗时间的药物和药物组合而进行的合理努力,应该将现有和实验性抗结核药物进入感染不同部位特定生理状态下的细菌的能力的知识,以及避免被外排或被宿主或细菌代谢灭活的知识,纳入其中。然而,虽然在强制性人类宿主的背景下理解任何现有或实验性抗结核药物的作用机制和药理学特性是基本要求,但这很复杂,而且直到最近,由于可用的方法和模型有限,这种要求一直受到严重限制。在这里,我们讨论了分析模型和技术的进展,这些进展使人们能够对新的结核药物开发进行药物代谢和药代动力学(DMPK)的研究。特别是,我们考虑了将传统药代动力学-药效学分析的重点从血浆转移到更具体的“作用部位”药物暴露的可能性,这是药物开发和给药策略设计的基本标准。此外,在总结确定包含宿主巨噬细胞和细胞内细菌的“感染单位”的 DMPK 数据的方法时,我们评估了在临床前药物开发算法的早期阶段包括这些分析的潜在好处。 2018 IUBMB Life,70(9):926-937,2018。