Microbiota and Drug Response in Inflammatory Bowel Disease

被引:26
|
作者
Franzin, Martina [1 ]
Stefancic, Katja [2 ]
Lucafo, Marianna [3 ]
Decorti, Giuliana [1 ,3 ]
Stocco, Gabriele [2 ]
机构
[1] Univ Trieste, Dept Med Surg & Hlth Sci, I-34127 Trieste, Italy
[2] Univ Trieste, Dept Life Sci, I-34127 Trieste, Italy
[3] Inst Maternal & Child Hlth IRCCS Burlo Garofolo, I-34137 Trieste, Italy
来源
PATHOGENS | 2021年 / 10卷 / 02期
关键词
microbiota; microbiome; inflammatory bowel disease; pharmacotherapy; COLONIC BACTERIAL METABOLISM; ANTI-TNF THERAPY; 5-AMINOSALICYLIC ACID; GUT MICROBIOTA; CROHNS-DISEASE; INTESTINAL MICROBIOTA; ULCERATIVE-COLITIS; COMMENSAL BACTERIA; CLINICAL-PRACTICE; BARRIER FUNCTION;
D O I
10.3390/pathogens10020211
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A mutualistic relationship between the composition, function and activity of the gut microbiota (GM) and the host exists, and the alteration of GM, sometimes referred as dysbiosis, is involved in various immune-mediated diseases, including inflammatory bowel disease (IBD). Accumulating evidence suggests that the GM is able to influence the efficacy of the pharmacological therapy of IBD and to predict whether individuals will respond to treatment. Additionally, the drugs used to treat IBD can modualate the microbial composition. The review aims to investigate the impact of the GM on the pharmacological therapy of IBD and vice versa. The GM resulted in an increase or decrease in therapeutic responses to treatment, but also to biotransform drugs to toxic metabolites. In particular, the baseline GM composition can help to predict if patients will respond to the IBD treatment with biologic drugs. On the other hand, drugs can affect the GM by incrementing or reducing its diversity and richness. Therefore, the relationship between the GM and drugs used in the treatment of IBD can be either beneficial or disadvantageous.
引用
收藏
页码:1 / 28
页数:28
相关论文
共 50 条
  • [41] Microbiota as key factors in inflammatory bowel disease
    White, Zachary
    Cabrera, Ivan
    Kapustka, Isabel
    Sano, Teruyuki
    FRONTIERS IN MICROBIOLOGY, 2023, 14
  • [42] Host–microbiota interactions in inflammatory bowel disease
    Markus F. Neurath
    Nature Reviews Gastroenterology & Hepatology, 2020, 17 : 76 - 77
  • [43] Gut Microbiota, Probiotics and Inflammatory Bowel Disease
    Johannes Stephani
    Katarina Radulovic
    Jan Hendrik Niess
    Archivum Immunologiae et Therapiae Experimentalis, 2011, 59 : 161 - 177
  • [44] Inflammatory bowel disease: between genetics and microbiota
    Nour Younis
    Rana Zarif
    Rami Mahfouz
    Molecular Biology Reports, 2020, 47 : 3053 - 3063
  • [45] Current evidence and clinical relevance of drug-microbiota interactions in inflammatory bowel disease
    Becker, Heike E. F.
    Demers, Karlijn
    Derijks, Luc J. J.
    Jonkers, Daisy M. A. E.
    Penders, John
    FRONTIERS IN MICROBIOLOGY, 2023, 14
  • [46] An (Anti)-Inflammatory Microbiota: Defining the Role in Inflammatory Bowel Disease?
    Burman, S.
    Hoedt, E. C.
    Pottenger, S.
    Mohd-Najman, N-S
    Cuiv, P. O.
    Morrison, Mark
    DIGESTIVE DISEASES, 2016, 34 (1-2) : 64 - 71
  • [47] TREATMENT RESPONSE TO USTEKINUMAB AND VEDOLIZUMAB IN INFLAMMATORY BOWEL DISEASE: THE PREDICTIVE ROLE OF GUT MICROBIOTA
    Caenepeel, Clara
    Vieira-Silva, Sara
    Vazquez-Castellanos, Jorge F.
    Verstockt, Bram
    Ferrante, Marc
    Raes, Jeroen
    Vermeire, Severine
    GASTROENTEROLOGY, 2019, 156 (06) : S1124 - S1124
  • [48] The predictive role of gut microbiota in treatment response to vedolizumab and ustekinumab in inflammatory bowel disease
    Caenepeel, C.
    Vieira-Silva, S.
    Verstockt, B.
    Ferrante, M.
    Raes, J.
    Vermeire, S.
    JOURNAL OF CROHNS & COLITIS, 2019, 13 : S542 - S542
  • [49] Drug interactions in inflammatory bowel disease
    Irving, Peter M.
    Shanahan, Fergus
    Rampton, David S.
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2008, 103 (01): : 207 - 219
  • [50] Intestinal microbiota pathogenesis and fecal microbiota transplantation for inflammatory bowel disease
    Wang, Zi-Kai
    Yang, Yun-Sheng
    Chen, Ye
    Yuan, Jing
    Sun, Gang
    Peng, Li-Hua
    WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (40) : 14805 - 14820