Literature DB >> 27634185

The Gut Microbiota and the Emergence of Autoimmunity: Relevance to Major Psychiatric Disorders.

Emily G Severance1, Dag Tveiten, Lief H Lindström, Robert H Yolken, Karl L Reichelt.   

Abstract

BACKGROUND: Autoimmune phenotypes are prevalent in major psychiatric disorders. Disequilibria of cellular processes occurring in the gastrointestinal (GI) tract likely contribute to immune dysfunction in psychiatric disorders. As the venue of a complex community of resident microbes, the gut in a homeostatic state equates with a functional digestive system, cellular barrier stability and properly regulated recognition of self and non-self antigens. When gut processes become disrupted as a result of environmental or genetic factors, autoimmunity may ensue.
METHODS: Here, we review the issues pertinent to autoimmunity and the microbiome in psychiatric disorders and show that many of the reported immune risk factors for the development of these brain disorders are in fact related and consistent with dysfunctions occurring in the gut. We review the few human microbiome studies that have been done in people with psychiatric disorders and supplement this information with mechanistic data gleaned from experimental rodent studies.
RESULTS: These investigations demonstrate changes in behavior and brain biochemistry directly attributable to alterations in the gut microbiome. We present a model by which autoantigens are produced by extrinsicallyderived food and microbial factors bound to intrinsic components of the gut including receptors present in the enteric nervous system.
CONCLUSION: This new focus on examining activities outside of the CNS for relevance to the etiology and pathophysiology of psychiatric disorders may require new modalities or a re-evaluation of pharmaceutical targets found in peripheral systems.

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Mesh:

Year:  2016        PMID: 27634185      PMCID: PMC5506689          DOI: 10.2174/1381612822666160914183804

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  215 in total

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5.  [Clinico-immunologic correlations in the period of development of therapeutical remissions in continuous forms of schizophrenia].

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