Department of Microbiology & Immunology, University of California San Francisco (UCSF), San Francisco, CA 94143, USA.
Department of Microbiology & Immunology, University of California San Francisco (UCSF), San Francisco, CA 94143, USA; Chan Zuckerberg Biohub, San Francisco, CA 94143, USA.
Cell Host Microbe. 2019 Jul 10;26(1):22-34. doi: 10.1016/j.chom.2019.06.011.
Despite the recognition, nearly a century ago, that the human microbiome plays a clinically relevant role in drug disposition, mechanistic insights, and translational applications are still limited. Here, we highlight the recent re-emergence of "pharmacomicrobiomics," which seeks to understand how inter-individual variations in the microbiome shape drug efficacy and side effect profiles. Multiple bacterial species, genes, and enzymes have already been implicated in the direct biotransformation of drugs, both from targeted case studies and from systematic computational and experimental analyses. Indirect mechanisms are also at play; for example, microbial interactions with the host immune system can have broad effects on immunomodulatory drugs. Finally, we discuss multiple emerging strategies for the precise manipulation of complex microbial communities to improve treatment outcomes. In the coming years, we anticipate a shift toward a more comprehensive view of precision medicine that encompasses our human and microbial genomes and their combined metabolic activities.
尽管近一个世纪前就已经认识到人类微生物组在药物处置、机制见解和转化应用中具有临床相关作用,但仍存在一定的局限性。在这里,我们强调了最近重新出现的“药物微生物组学”,它旨在了解个体间微生物组的差异如何影响药物的疗效和副作用特征。从有针对性的案例研究和系统的计算和实验分析中,已经发现多种细菌物种、基因和酶直接参与药物的生物转化。间接机制也在起作用;例如,微生物与宿主免疫系统的相互作用可以对免疫调节药物产生广泛的影响。最后,我们讨论了多种新兴策略,用于精确操纵复杂的微生物群落,以改善治疗效果。在未来几年,我们预计将朝着更全面的精准医学观点转变,其中包括我们的人类和微生物基因组及其组合代谢活动。