Fecal transplants in spondyloarthritis and uveitis: ready for a clinical trial?

被引:17
作者
Choi, Rene Y. [1 ]
Asquith, Mark [2 ]
Rosenbaum, James T. [1 ,2 ,3 ]
机构
[1] Oregon Hlth & Sci Univ, Casey Eye Inst, Dept Ophthalmol, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Ophthalmol, Div Arthrit & Rheumat Dis, 3181 SW Sam Jackson Pk Rd,L467Ad, Portland, OR 97239 USA
[3] Legacy Devers Eye Inst, Portland, OR USA
关键词
ankylosing spondylitis; HLA-B27; microbiome; spondyloarthritis; uveitis; HLA-B27 TRANSGENIC RATS; RANDOMIZED CONTROLLED-TRIAL; INFLAMMATORY-BOWEL-DISEASE; ACTIVE ULCERATIVE-COLITIS; HL-A; 27; ANKYLOSING-SPONDYLITIS; REACTIVE ARTHRITIS; GUT MICROBIOTA; CROHNS-DISEASE; PSORIATIC-ARTHRITIS;
D O I
10.1097/BOR.0000000000000506
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The intestinal microbiome is thought to play a role in the pathogenesis of inflammatory bowel disease (IBD). There are many shared clinical manifestations between IBD and spondyloarthritis (SpA), of which the most common are peripheral arthritis and uveitis. Clinical overlap along with similar genetics between these diseases suggests a possible shared pathogenetic mechanism, which might center on the intestinal microbiota. In this review, we discuss the available evidence that SpA is a microbiome-driven disease and indicate how SpA-associated uveitis could be tied to gut dysbiosis. We conclude by discussing different treatment paradigms targeting the intestinal microbiome for SpA. Recent findings Recent studies support the growing evidence of the intestinal microbiome as a crucial player in SpA disease pathogenesis. There is emerging evidence that the gut microbiome may play a causative role in uveitis. Summary The field is beginning to discover a new level of understanding how the intestinal microbiome is involved in SpA. Treatment methods to alter intestinal microbiota to treat SpA-related diseases are still in its infancy.
引用
收藏
页码:303 / 309
页数:7
相关论文
共 97 条
[1]  
Aiko S, 1998, J PHARMACOL EXP THER, V284, P722
[2]  
Ajene AN, 2013, J HEALTH POPUL NUTR, V31, P299
[3]   Intestinal Metabolites Are Profoundly Altered in the Context of HLA-B27 Expression and Functionally Modulate Disease in a Rat Model of Spondyloarthritis [J].
Asquith, Mark ;
Davin, Sean ;
Stauffer, Patrick ;
Michell, Claire ;
Janowitz, Cathleen ;
Lin, Phoebe ;
Ensign-Lewis, Joe ;
Kinchen, Jason M. ;
Koop, Dennis R. ;
Rosenbaum, James T. .
ARTHRITIS & RHEUMATOLOGY, 2017, 69 (10) :1984-1995
[4]   The interaction between host genetics and the microbiome in the pathogenesis of spondyloarthropathies [J].
Asquith, Mark ;
Rosenbaum, James T. .
CURRENT OPINION IN RHEUMATOLOGY, 2016, 28 (04) :405-412
[5]   Perturbed Mucosal Immunity and Dysbiosis Accompany Clinical Disease in a Rat Model of Spondyloarthritis [J].
Asquith, Mark J. ;
Stauffer, Patrick ;
Davin, Sean ;
Mitchell, Claire ;
Lin, Phoebe ;
Rosenbaum, James T. .
ARTHRITIS & RHEUMATOLOGY, 2016, 68 (09) :2151-2162
[6]  
Bäckhed F, 2015, CELL HOST MICROBE, V17, P690, DOI [10.1016/j.chom.2015.04.004, 10.1016/j.chom.2015.05.012]
[7]   Methods and Reporting Studies Assessing Fecal Microbiota Transplantation A Systematic Review [J].
Bafeta, Aida ;
Yavchitz, Amelie ;
Riveros, Carolina ;
Batista, Rui ;
Ravaud, Philippe .
ANNALS OF INTERNAL MEDICINE, 2017, 167 (01) :34-+
[8]  
BAYEN H, 1988, J FR OPHTALMOL, V11, P561
[9]   Interleukin-23 Mediates the Intestinal Response to Microbial β-1,3-Glucan and the Development of Spondyloarthritis Pathology in SKG Mice [J].
Benham, Helen ;
Rehaume, Linda M. ;
Hasnain, Sumaira Z. ;
Velasco, Jared ;
Baillet, Athan C. ;
Ruutu, Merja ;
Kikly, Kristine ;
Wang, Ran ;
Tseng, Hsu-Wen ;
Thomas, Gethin P. ;
Brown, Matthew A. ;
Strutton, Geoffrey ;
McGuckin, Michael A. ;
Thomas, Ranjeny .
ARTHRITIS & RHEUMATOLOGY, 2014, 66 (07) :1755-1767
[10]   Faecal microbiota study reveals specific dysbiosis in spondyloarthritis [J].
Breban, Maxime ;
Tap, Julien ;
Leboime, Ariane ;
Said-Nahal, Roula ;
Langella, Philippe ;
Chiocchia, Gilles ;
Furet, Jean-Pierre ;
Sokol, Harry .
ANNALS OF THE RHEUMATIC DISEASES, 2017, 76 (09) :1614-1622