The Future of Microbiome-Based Therapeutics in Clinical Applications

被引:37
作者
Sharma, Anukriti [1 ,2 ]
Das, Promi [1 ,2 ]
Buschmann, Mary [1 ,2 ]
Gilbert, Jack A. [1 ,2 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Pediat, La Jolla, CA 92093 USA
[2] UCSD, Scripps Inst Oceanog, La Jolla, CA 92103 USA
关键词
ACTIVE ULCERATIVE-COLITIS; GUT MICROBIOME; INTESTINAL MICROBIOTA; IRINOTECAN CPT-11; TRANSPLANTATION; METABOLISM; BACTERIA; CANCER; DONOR; EFFICACY;
D O I
10.1002/cpt.1677
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The microbiome, a collection of microorganisms, their genomes, and the surrounding environmental conditions, is akin to a human organ, and knowledge is emerging on its role in human health and diseases. The influence of the microbiome in drug response has only been investigated in detail for the last 10 years. The human microbiome is a complex and highly dynamic system, which varies dramatically between individuals, yet there exists a common core microbiome that is heritable and can be transmitted to progeny. Here, we review the role of the human microbiome, which is now widely accepted as a major factor that drives the interpersonal variation in therapeutic response. We describe examples in which the microbiome modifies drug action. Despite its complexity, the microbiome can be readily altered, with the potential to increase the benefits and reduce the toxicity and side effects associated with pharmaceutical drugs. The potential of new microbiome-based strategies, such as fecal microbiota transplant, probiotics, and phage therapy, as promising medical therapeutics are outlined. We also suggest a combination reductionist and system-level approaches that could be applied to further investigate the role of microbiota in drug metabolism modulation of drug response. Finally, we emphasize the importance of combining microbiome and pharmacology studies as a novel means to treat disease and reduce side effects.
引用
收藏
页码:123 / 128
页数:6
相关论文
共 89 条
[1]  
Aldrich AM, 2019, PEDIATR INFECT DIS J, V38, P32, DOI [10.1097/inf.0000000000002053, 10.1097/INF.0000000000002053]
[2]   Gut microbiota modulation of chemotherapy efficacy and toxicity [J].
Alexander, James L. ;
Wilson, Ian D. ;
Teare, Julian ;
Marchesi, Julian R. ;
Nicholson, Jeremy K. ;
Kinross, James M. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2017, 14 (06) :356-365
[3]  
[Anonymous], BRIEF FDA WARNS POT
[4]  
[Anonymous], 538215 BIORXIV
[5]   PharmacoMicrobiomics or how bugs modulate drugs: an educational initiative to explore the effects of human microbiome on drugs [J].
Aziz, Ramy K. ;
Saad, Rama ;
Rizkallah, Mariam R. .
BMC BIOINFORMATICS, 2011, 12
[6]   Fecal Microbiota Transplant From a Rational Stool Donor Improves Hepatic Encephalopathy: A Randomized Clinical Trial [J].
Bajaj, Jasmohan S. ;
Kassam, Zain ;
Fagan, Andrew ;
Gavis, Edith A. ;
Liu, Eric ;
Cox, I. Jane ;
Kheradman, Raffi ;
Heuman, Douglas ;
Wang, Jessica ;
Gurry, Thomas ;
Williams, Roger ;
Sikaroodi, Masoumeh ;
Fuchs, Michael ;
Alm, Eric ;
John, Binu ;
Thacker, Leroy R. ;
Riva, Antonio ;
Smith, Mark ;
Taylor-Robinson, Simon D. ;
Gillevet, Patrick M. .
HEPATOLOGY, 2017, 66 (06) :1727-1738
[7]   Role of the Microbiota in Immunity and Inflammation [J].
Belkaid, Yasmine ;
Hand, Timothy W. .
CELL, 2014, 157 (01) :121-141
[8]   Towards a more comprehensive concept for prebiotics [J].
Bindels, Laure B. ;
Delzenne, Nathalie M. ;
Cani, Patrice D. ;
Walter, Jens .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2015, 12 (05) :303-310
[9]   How to Determine the Role of the Microbiome in Drug Disposition [J].
Bisanz, Jordan E. ;
Spanogiannopoulos, Peter ;
Pieper, Lindsey M. ;
Bustion, Annamarie E. ;
Turnbaugh, Peter J. .
DRUG METABOLISM AND DISPOSITION, 2018, 46 (11) :1588-1595
[10]   VSL#3 probiotic treatment reduces chemotherapy-induced diarrhea and weight loss [J].
Bowen, Joanne M. ;
Stringer, Andrea M. ;
Gibson, Rachel J. ;
Yeoh, Ann S. J. ;
Hannam, Sarah ;
Keefe, Dorothy M. K. .
CANCER BIOLOGY & THERAPY, 2007, 6 (09) :1449-1454