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The Gut Microbiota in Immune-Mediated Inflammatory Diseases

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2016 Jul 28
PMID 27462309
Citations 210
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Abstract

The collection of microbes and their genes that exist within and on the human body, collectively known as the microbiome has emerged as a principal factor in human health and disease. Humans and microbes have established a symbiotic association over time, and perturbations in this association have been linked to several immune-mediated inflammatory diseases (IMID) including inflammatory bowel disease, rheumatoid arthritis, and multiple sclerosis. IMID is a term used to describe a group of chronic, highly disabling diseases that affect different organ systems. Though a cornerstone commonality between IMID is the idiopathic nature of disease, a considerable portion of their pathobiology overlaps including epidemiological co-occurrence, genetic susceptibility loci and environmental risk factors. At present, it is clear that persons with an IMID are at an increased risk for developing comorbidities, including additional IMID. Advancements in sequencing technologies and a parallel explosion of 16S rDNA and metagenomics community profiling studies have allowed for the characterization of microbiomes throughout the human body including the gut, in a myriad of human diseases and in health. The main challenge now is to determine if alterations of gut flora are common between IMID or, if particular changes in the gut community are in fact specific to a single disease. Herein, we review and discuss the relationships between the gut microbiota and IMID.

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References
1.
Quera R, Espinoza R, Estay C, Rivera D . Bacteremia as an adverse event of fecal microbiota transplantation in a patient with Crohn's disease and recurrent Clostridium difficile infection. J Crohns Colitis. 2013; 8(3):252-3. DOI: 10.1016/j.crohns.2013.10.002. View

2.
Chen J, Wright K, Davis J, Jeraldo P, Marietta E, Murray J . An expansion of rare lineage intestinal microbes characterizes rheumatoid arthritis. Genome Med. 2016; 8(1):43. PMC: 4840970. DOI: 10.1186/s13073-016-0299-7. View

3.
Bernstein C, Blanchard J, Houston D, Wajda A . The incidence of deep venous thrombosis and pulmonary embolism among patients with inflammatory bowel disease: a population-based cohort study. Thromb Haemost. 2001; 85(3):430-4. View

4.
Sokol H, Leducq V, Aschard H, Pham H, Jegou S, Landman C . Fungal microbiota dysbiosis in IBD. Gut. 2016; 66(6):1039-1048. PMC: 5532459. DOI: 10.1136/gutjnl-2015-310746. View

5.
Guerrero C, Tort J, Perez J, Andres M, Espejo E . Rhodococcus equi infection in a patient with Crohn's disease treated with infliximab. J Infect. 2014; 70(6):689-90. DOI: 10.1016/j.jinf.2014.12.008. View