TY - JOUR
T1 - The emerging microbiome-based approaches to IBD therapy
T2 - From SCFAs to urolithin A
AU - Rudiansyah, Mohammad
AU - Abdalkareem Jasim, Saade
AU - S. Azizov, Bakhadir
AU - Samusenkov, Vadim
AU - Kamal Abdelbasset, Walid
AU - Yasin, Ghulam
AU - Mohammad, Hawraa Jabbar
AU - Jawad, Mohammed Abed
AU - Mahmudiono, Trias
AU - Hosseini-Fard, Seyed Reza
AU - Mirzaei, Rasoul
AU - Karampoor, Sajad
N1 - Publisher Copyright:
© 2022 Chinese Medical Association Shanghai Branch, Chinese Society of Gastroenterology, Renji Hospital Affiliated to Shanghai Jiaotong University School of Medicine and John Wiley & Sons Australia, Ltd.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Inflammatory bowel disease (IBD) is a group of chronic gastrointestinal inflammatory conditions which can be life-threatening, affecting both children and adults. Crohn's disease and ulcerative colitis are the two main forms of IBD. The pathogenesis of IBD is complex and involves genetic background, environmental factors, alteration in gut microbiota, aberrant immune responses (innate and adaptive), and their interactions, all of which provide clues to the identification of innovative diagnostic or prognostic biomarkers and the development of novel treatments. Gut microbiota provide significant benefits to its host, most notably via maintaining immunological homeostasis. Furthermore, changes in gut microbial populations may promote immunological dysregulation, resulting in autoimmune diseases, including IBD. Investigating the interaction between gut microbiota and immune system of the host may lead to a better understanding of the pathophysiology of IBD as well as the development of innovative immune- or microbe-based therapeutics. In this review we summarized the most recent findings on innovative therapeutics for IBD, including microbiome-based therapies such as fecal microbiota transplantation, probiotics, live biotherapeutic products, short-chain fatty acids, bile acids, and urolithin A.
AB - Inflammatory bowel disease (IBD) is a group of chronic gastrointestinal inflammatory conditions which can be life-threatening, affecting both children and adults. Crohn's disease and ulcerative colitis are the two main forms of IBD. The pathogenesis of IBD is complex and involves genetic background, environmental factors, alteration in gut microbiota, aberrant immune responses (innate and adaptive), and their interactions, all of which provide clues to the identification of innovative diagnostic or prognostic biomarkers and the development of novel treatments. Gut microbiota provide significant benefits to its host, most notably via maintaining immunological homeostasis. Furthermore, changes in gut microbial populations may promote immunological dysregulation, resulting in autoimmune diseases, including IBD. Investigating the interaction between gut microbiota and immune system of the host may lead to a better understanding of the pathophysiology of IBD as well as the development of innovative immune- or microbe-based therapeutics. In this review we summarized the most recent findings on innovative therapeutics for IBD, including microbiome-based therapies such as fecal microbiota transplantation, probiotics, live biotherapeutic products, short-chain fatty acids, bile acids, and urolithin A.
KW - bile acids and salts
KW - inflammatory bowel diseases
KW - microbiome-based therapy
KW - probiotics
KW - urolithin A
UR - http://www.scopus.com/inward/record.url?scp=85142289842&partnerID=8YFLogxK
U2 - 10.1111/1751-2980.13131
DO - 10.1111/1751-2980.13131
M3 - Review article
C2 - 36178158
AN - SCOPUS:85142289842
SN - 1751-2972
VL - 23
SP - 412
EP - 434
JO - Journal of Digestive Diseases
JF - Journal of Digestive Diseases
IS - 8-9
ER -