β-内酰胺和β-内酰胺酶抑制剂联合耐药性发展的半机制建模。

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Journal of Pharmacokinetics and Pharmacodynamics Pub Date : 2024-06-01 Epub Date: 2023-11-26 DOI:10.1007/s10928-023-09895-3
Sebastian T Tandar, Linda B S Aulin, Eva M J Leemkuil, Apostolos Liakopoulos, J G Coen van Hasselt
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引用次数: 0

摘要

β-内酰胺(BL)和β-内酰胺酶抑制剂(BLI)联合使用,如哌拉西林-他唑巴坦(PIP-TAZ)是对抗广谱β-内酰胺酶产生菌感染的有效策略。然而,在革兰氏阴性菌中,对BL-BLI组合的耐药性(包括突变和适应性)仍然可以通过多种机制发展。这些机制可能包括增加β-内酰胺酶活性,减少药物流入和增加药物外排。了解这些机制在耐药发展过程中的相对作用,有助于确定设计抗BL-BLI耐药治疗方案时最有效的靶向机制。本研究采用半机制数学模型结合抗生素敏感性试验,评估表达CTX-M-15和SHV-1 β-内酰胺酶的肺炎克雷伯菌分离株在PIP-TAZ耐药发展过程中不同耐药机制的潜在影响。数学模型被用来评估几种细胞变化作为PIP-TAZ抗性的唯一介质的潜在影响。我们的半机制模型确定了13种被检查机制中的2种作为可能独立支持观察到的PIP-TAZ阻力大小的关键阻力机制,即孔蛋白损失和外排泵上调。利用所得到的模型进行的模拟也表明,PIP-TAZ的剂量可能会在其常用的8:1给药比之外进行调整。目前的研究表明,基于理论的机制模型可以通过实验数据来支持关于潜在抗性机制的假设生成,这可能指导后续的实验研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Semi-mechanistic modeling of resistance development to β-lactam and β-lactamase-inhibitor combinations.

The use of β-lactam (BL) and β-lactamase inhibitor (BLI) combinations, such as piperacillin-tazobactam (PIP-TAZ) is an effective strategy to combat infections by extended-spectrum β-lactamase-producing bacteria. However, in Gram-negative bacteria, resistance (both mutational and adaptive) to BL-BLI combination can still develop through multiple mechanisms. These mechanisms may include increased β-lactamase activity, reduced drug influx, and increased drug efflux. Understanding the relative contribution of these mechanisms during resistance development helps identify the most impactful mechanism to target in designing a treatment to counter BL-BLI resistance. This study used semi-mechanistic mathematical modeling in combination with antibiotic sensitivity assays to assess the potential impact of different resistance mechanisms during the development of PIP-TAZ resistance in a Klebsiella pneumoniae isolate expressing CTX-M-15 and SHV-1 β-lactamases. The mathematical models were used to evaluate the potential impact of several cellular changes as a sole mediator of PIP-TAZ resistance. Our semi-mechanistic model identified 2 out of the 13 inspected mechanisms as key resistance mechanisms that may independently support the observed magnitude of PIP-TAZ resistance, namely porin loss and efflux pump up-regulation. Simulation using the resulting models also suggested the possible adjustment of PIP-TAZ dose outside its commonly used 8:1 dosing ratio. The current study demonstrated how theory-based mechanistic models informed by experimental data can be used to support hypothesis generation regarding potential resistance mechanisms, which may guide subsequent experimental studies.

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来源期刊
CiteScore
4.90
自引率
4.00%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Broadly speaking, the Journal of Pharmacokinetics and Pharmacodynamics covers the area of pharmacometrics. The journal is devoted to illustrating the importance of pharmacokinetics, pharmacodynamics, and pharmacometrics in drug development, clinical care, and the understanding of drug action. The journal publishes on a variety of topics related to pharmacometrics, including, but not limited to, clinical, experimental, and theoretical papers examining the kinetics of drug disposition and effects of drug action in humans, animals, in vitro, or in silico; modeling and simulation methodology, including optimal design; precision medicine; systems pharmacology; and mathematical pharmacology (including computational biology, bioengineering, and biophysics related to pharmacology, pharmacokinetics, orpharmacodynamics). Clinical papers that include population pharmacokinetic-pharmacodynamic relationships are welcome. The journal actively invites and promotes up-and-coming areas of pharmacometric research, such as real-world evidence, quality of life analyses, and artificial intelligence. The Journal of Pharmacokinetics and Pharmacodynamics is an official journal of the International Society of Pharmacometrics.
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