Abstract

One of the main tasks of the immune system is to discriminate and appropriately react to “danger” or “non-danger” signals. This is crucial in the gastrointestinal tract, where the immune system is confronted with a myriad of food antigens and symbiotic microflora that are in constant contact with the mucosa, in addition to any potential pathogens. This large number of antigens and commensal microflora, which are essential for providing vital nutrients, must be tolerated by the intestinal immune system to prevent aberrant inflammation. Hence, the balance between immune activation versus tolerance should be tightly regulated to maintain intestinal homeostasis and to prevent immune activation indiscriminately against all luminal antigens. Loss of this delicate equilibrium can lead to chronic activation of the intestinal immune response resulting in intestinal disorders, such as inflammatory bowel diseases (IBD). In order to maintain homeostasis, the immune system has evolved diverse regulatory strategies including additional non-immunological actors able to control the immune response. Accumulating evidence strongly indicates a bidirectional link between the two systems in which the brain modulates the immune response via the detection of circulating cytokines and via direct afferent input from sensory fibers and from enteric neurons. In the current review, we will highlight the most recent findings regarding the cross-talk between the nervous system and the mucosal immune system and will discuss the potential use of these neuronal circuits and neuromediators as novel therapeutic tools to reestablish immune tolerance and treat intestinal chronic inflammation.

Highlights

  • A main function of the immune system is to distinguish between “danger” or “non-danger” signals and to respond appropriately. This is crucial in the gastrointestinal (GI) tract, where the immune system is constantly exposed to a multitude of food antigens and symbiotic microflora, which are essential for providing vital nutrients to the body

  • An intricate network of immune and non-immune cells and their mediators function in unison to protect us from toxic elements and infectious microbial diseases that are encountered in the intestinal lumen

  • On occasion alterations of the steady state due to genetic background and/or environmental microbes result in inflammatory diseases or infections including development of inflammatory bowel diseases (IBD)

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Summary

INTESTINAL IMMUNE HOMEOSTASIS AND ORAL TOLERANCE

A main function of the immune system is to distinguish between “danger” or “non-danger” signals and to respond appropriately. In individuals with genetic or environmental predisposition (altered microbiota, viral or bacterial infection, chemical additives, or pollution) oral tolerance is broken resulting in immune activation against luminal antigens. Loss of this delicate equilibrium indiscriminately results in chronic and excessive immune activation indiscriminately against luminal antigens leading to invalidating intestinal disorders, such as inflammatory bowel disease (IBD). We will discuss the potential employment of some of these neuronal circuits and neuromediators as novel therapeutic tools to reestablish immune tolerance and treat intestinal chronic inflammatory diseases, such as IBD

THE NERVOUS SYSTEM AS MODULATOR OF IMMUNE RESPONSE
NEUROIMMUNE INTERACTION IN THE GUT WALL
PARASYMPATHETIC NERVOUS SYSTEM AS MODULATOR OF INTESTINAL IMMUNE HOMEOSTASIS
SYMPATHETIC NERVOUS SYSTEM
VASOACTIVE INTESTINAL PEPTIDE
NEUROPEPTIDE Y
Clinical evidence
No clinical evidence available
SUBSTANCE P
CONCLUSION AND PERSPECTIVE
Full Text
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