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Does the microbiota play a role in the pathogenesis of autoimmune diseases

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TLDR
This review summarises the current status on the role of the microbiota in autoimmune diseases and offers novel insight into factors that initiate and drive disease progression, stratify patient risk for complications and ultimately deliver new therapeutic strategies.
Abstract
The microbiota of the human metaorganism is not a mere bystander. These microbes have coevolved with us and are pivotal to normal development and homoeostasis. Dysbiosis of the GI microbiota is associated with many disease susceptibilities, including obesity, malignancy, liver disease and GI pathology such as IBD. It is clear that there is direct and indirect crosstalk between this microbial community and host immune response. However, the precise mechanism of this microbial influence in disease pathogenesis remains elusive and is now a major research focus. There is emerging literature on the role of the microbiota in the pathogenesis of autoimmune disease, with clear and increasing evidence that changes in the microbiota are associated with some of these diseases. Examples include type 1 diabetes, coeliac disease and rheumatoid arthritis, and these contribute significantly to global morbidity and mortality. Understanding the role of the microbiota in autoimmune diseases may offer novel insight into factors that initiate and drive disease progression, stratify patient risk for complications and ultimately deliver new therapeutic strategies. This review summarises the current status on the role of the microbiota in autoimmune diseases.

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Journal ArticleDOI

Current Understanding of Dysbiosis in Disease in Human and Animal Models.

TL;DR: This review article has focused on explaining the multiple types of dysbiosis, as well as Dysbiosis-related diseases and potential treatments to apply this knowledge to understand a possible cause and potentially find therapeutic strategies for IBD aswell as the other dysbiotic- related diseases.
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Stress and the Microbiota-Gut-Brain Axis in Visceral Pain: Relevance to Irritable Bowel Syndrome.

TL;DR: This review will highlight the evidence by which stress and the gut microbiota interact in the regulation of visceral nociception and the mechanisms by which microbiota can affect the stress response and behavioral outcomes with an emphasis on visceral pain.
Journal ArticleDOI

Novel players in coeliac disease pathogenesis: role of the gut microbiota

TL;DR: The importance of utilizing animal models and long-term clinical studies to gain insight into the mechanisms through which host–microbial interactions can influence host responses to gluten and how the interplay between host genetics, environmental factors and the intestinal microbiota might contribute to its pathogenesis is highlighted.
Journal ArticleDOI

Gut-lung axis: The microbial contributions and clinical implications.

TL;DR: The impact of gut and lung microbiota on disease exacerbation and progression, and the recent understanding of the immunological link between the gut and the lung, the gut–lung axis are discussed.
References
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Journal ArticleDOI

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Curtis Huttenhower, +253 more
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TL;DR: The Human Microbiome Project Consortium reported the first results of their analysis of microbial communities from distinct, clinically relevant body habitats in a human cohort; the insights into the microbial communities of a healthy population lay foundations for future exploration of the epidemiology, ecology and translational applications of the human microbiome as discussed by the authors.
Journal Article

Structure, function and diversity of the healthy human microbiome

Curtis Huttenhower, +247 more
- 01 Jun 2012 - 
TL;DR: The Human Microbiome Project has analysed the largest cohort and set of distinct, clinically relevant body habitats so far, finding the diversity and abundance of each habitat’s signature microbes to vary widely even among healthy subjects, with strong niche specialization both within and among individuals.
Journal ArticleDOI

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Journal ArticleDOI

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TL;DR: The increased understanding of the immune mechanisms of rheumatoid arthritis has led to the development of a considerable number of new therapeutic agents that alter the natural history of the disease and reduce mortality.
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