Abstract

The dense innervation of the gastro-intestinal tract with neuronal networks, which are in close proximity to immune cells, implies a pivotal role of neurons in modulating immune functions. Neurons have the ability to directly sense danger signals, adapt immune effector functions and integrate these signals to maintain tissue integrity and host defense strategies. The expression pattern of a large set of immune cells in the intestine characterized by receptors for neurotransmitters and neuropeptides suggest a tight neuronal hierarchical control of immune functions in order to systemically control immune reactions. Compelling evidence implies that targeting neuro-immune interactions is a promising strategy to dampen immune responses in autoimmune diseases such as inflammatory bowel diseases or rheumatoid arthritis. In fact, electric stimulation of vagal fibers has been shown to be an extremely effective treatment strategy against overwhelming immune reactions, even after exhausted conventional treatment strategies. Such findings argue that the nervous system is underestimated coordinator of immune reactions and underline the importance of neuro-immune crosstalk for body homeostasis. Herein, we review neuro-immune interactions with a special focus on disease pathogenesis throughout the gastro-intestinal tract.

Highlights

  • Immune responses at mucosal barriers are of particular interest because the mucosa is the primary entry port for many pathogens as well as the major site for chronic and sometimes detrimental immune responses

  • The therapeutic potential of neuronal modulation of inflammation in humans was already demonstrated by stimulating the vagal nerve with electronic devices that has been successfully used for the treatment of rheumatoid arthritis and asthma [9, 164]

  • Some patients did no longer respond to a conventional anti-inflammatory treatment but developed disease improvement upon vagal nerve stimulation [9]

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Summary

Introduction

Immune responses at mucosal barriers are of particular interest because the mucosa is the primary entry port for many pathogens as well as the major site for chronic and sometimes detrimental immune responses. Preclinical studies targeting neuro-immune interactions upon stimulation of the vagus nerve, application of acetylcholine agonist, and β2 adrenoreceptor agonists have emerged the potential successful treatment in inflammatory diseases [155, 162, 163].

Results
Conclusion

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