TY - JOUR
T1 - A breakthrough in probiotics
T2 - Clostridium butyricum regulates gut homeostasis and anti-inflammatory response in inflammatory bowel disease
AU - Kanai, Takanori
AU - Mikami, Yohei
AU - Hayashi, Atsushi
N1 - Funding Information:
We thank Shinta Mizuno, Hiroki Kiyohara, Mari Arai, Mina Kitazume, Kozue Takeshita, Keiichiro Saigusa, Makoto Naganuma, Katsuyoshi Matsuoka, Toshiro Sato, and Tadakazu Hisamatsu (Keio University) for technical assistance and for valuable discussion. This study was supported in part by Grants-in-Aid for Scientific Research, Scientific Research on Priority Areas, Exploratory Research and Creative Scientific Research from the Japanese Ministry of Education, Culture, Sports, Science and Technology, the Japanese Ministry of Health, Labour and Welfare, and the Keio University Medical Fund.
Publisher Copyright:
© 2015, Springer Japan.
PY - 2015/9/11
Y1 - 2015/9/11
N2 - Intestinal immune homeostasis is regulated by gut microbiota, including beneficial and pathogenic microorganisms. Imbalance in gut bacterial constituents provokes host proinflammatory responses causing diseases such as inflammatory bowel disease (IBD). The development of next-generation sequencing technology allows the identification of microbiota alterations in IBD. Several studies have shown reduced diversity in the gut microbiota of patients with IBD. Advances in gnotobiotic technology have made possible analysis of the role of specific bacterial strains in immune cells in the intestine. Using these techniques, we have shown that Clostridium butyricum as a probiotic induces interleukin-10-producing macrophages in inflamed mucosa via the Toll-like receptor 2/myeloid differentiation primary response gene 88 pathway to prevent acute experimental colitis. In this review, we focus on the new approaches for the role of specific bacterial strains in immunological responses, as well as the potential of bacterial therapy for IBD treatments.
AB - Intestinal immune homeostasis is regulated by gut microbiota, including beneficial and pathogenic microorganisms. Imbalance in gut bacterial constituents provokes host proinflammatory responses causing diseases such as inflammatory bowel disease (IBD). The development of next-generation sequencing technology allows the identification of microbiota alterations in IBD. Several studies have shown reduced diversity in the gut microbiota of patients with IBD. Advances in gnotobiotic technology have made possible analysis of the role of specific bacterial strains in immune cells in the intestine. Using these techniques, we have shown that Clostridium butyricum as a probiotic induces interleukin-10-producing macrophages in inflamed mucosa via the Toll-like receptor 2/myeloid differentiation primary response gene 88 pathway to prevent acute experimental colitis. In this review, we focus on the new approaches for the role of specific bacterial strains in immunological responses, as well as the potential of bacterial therapy for IBD treatments.
KW - Clostridium butyricum
KW - Interleukin-10
KW - Macrophages
KW - Probiotics
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U2 - 10.1007/s00535-015-1084-x
DO - 10.1007/s00535-015-1084-x
M3 - Review article
C2 - 25940150
AN - SCOPUS:84941261312
SN - 0944-1174
VL - 50
SP - 928
EP - 939
JO - Journal of Gastroenterology
JF - Journal of Gastroenterology
IS - 9
ER -