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Translational Development of Microbiome‐Based Therapeutics: Kinetics of E. coli Nissle and Engineered Strains in Humans and Nonhuman Primates

机译:基于微生物组的治疗学的转化发展:人类和非人类灵长类动物中大肠杆菌尼氏菌和工程菌的动力学

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摘要

Understanding the pharmacology of microbiome‐based therapeutics is required to support the development of new medicines. Strains of E. coli Nissle (EcN) were genetically modified and administered to cynomolgus monkeys at doses of 1 × 109 and 1 × 1012 colony‐forming units (CFU)/day for 28 days. A clinical study to evaluate the exposure and clearance of EcN in healthy volunteers was also performed. Healthy subjects received oral doses of EcN, 2.5 to 25 × 109 CFU 3 times daily for 28 days or a single day. In cynomolgus monkeys, replicating strains yielded higher fecal concentrations than nonreplicating strains and persisted for longer following cessation of dosing. In the clinical study, all subjects cleared EcN following cessation of dosing with median clearance of 1 week. Quantitative methodology can be applied to microbiome‐based therapeutics, and similar kinetics and clearance were observed for EcN in cynomolgus monkeys and humans.
机译:需要了解基于微生物组的疗法的药理学,以支持新药的开发。对大肠杆菌Nissle(EcN)菌株进行了基因修饰,并以1×10 9 和1×10 12 菌落形成单位(CFU)的剂量施用于食蟹猴/天,共28天。还进行了一项临床研究,以评估健康志愿者中EcN的暴露和清除情况。健康受试者每天口服EcN剂量为2.5到25×10 9 CFU 2.5次,连续28天或一天。在食蟹猴中,复制品比非复制品产生更高的粪便浓度,并且在停止给药后持续更长的时间。在临床研究中,所有受试者在中位清除时间为1周后停止用药后清除EcN。定量方法学可以应用于基于微生物组的治疗方法,并且食蟹猴和人类的EcN观察到相似的动力学和清除率。

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