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J. Clin. Med. 2017, 6(6), 60; doi:10.3390/jcm6060060

Role of Gut Microbiota in Rheumatoid Arthritis

1,2,3
and
1,2,*
1
Laboratory of Immune Regulation, Department of Microbiology and Immunology, Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan
2
Core Research for Evolutional Science and Technology, Japan Agency for Medical Research and Development, Tokyo 100-0004, Japan
3
Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, WPI Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan
*
Author to whom correspondence should be addressed.
Academic Editor: Shigeru Kotake
Received: 20 April 2017 / Revised: 1 June 2017 / Accepted: 6 June 2017 / Published: 9 June 2017
(This article belongs to the Special Issue Th17 Cell in Autoimmune and Inflammatory Diseases)
View Full-Text   |   Download PDF [393 KB, uploaded 9 June 2017]   |  

Abstract

Rheumatoid arthritis (RA) is a systemic autoimmune disease, caused by both genetic and environmental factors. Recently, investigators have focused on the gut microbiota, which is thought to be an environmental agent affecting the development of RA. Here we review the evidence from animal and human studies that supports the role of the gut microbiota in RA. We and others have demonstrated that the abundance of Prevotella copri is increased in some early RA. We have also used gnotobiotic experiments to show that dysbiosis in RA patients contributed to the development of Th17 cell-dependent arthritis in intestinal microbiota-humanized SKG mice. On the other hand, Prevotella histicola from human gut microbiota suppressed the development of arthritis. In summary, Prevotella species are involved in the pathogenesis of arthritis. View Full-Text
Keywords: rheumatoid arthritis; microbiota; Prevotella copri; gut; Th17 cell rheumatoid arthritis; microbiota; Prevotella copri; gut; Th17 cell
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Maeda, Y.; Takeda, K. Role of Gut Microbiota in Rheumatoid Arthritis. J. Clin. Med. 2017, 6, 60.

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