Probiotics in Autoimmune and Inflammatory Disorders

Nutrients. 2018 Oct 18;10(10):1537. doi: 10.3390/nu10101537.


Probiotics have been used to ameliorate gastrointestinal symptoms since ancient times. Over the past 40 years, probiotics have been shown to impact the immune system, both in vivo and in vitro. This interaction is linked to gut microbes, their polysaccharide antigens, and key metabolites produced by these bacteria. At least four metabolic pathways have been implicated in mechanistic studies of probiotics, based on mechanistic studies in animal models. Microbial⁻immune system crosstalk has been linked to: short-chain fatty acid production and signaling, tryptophan metabolism and the activation of aryl hydrocarbon receptors, nucleoside signaling in the gut, and activation of the intestinal histamine-2 receptor. Several randomized controlled trials have now shown that microbial modification by probiotics may improve gastrointestinal symptoms and multiorgan inflammation in rheumatoid arthritis, ulcerative colitis, and multiple sclerosis. Future work will need to carefully assess safety issues, selection of optimal strains and combinations, and attempts to prolong the duration of colonization of beneficial microbes.

Keywords: adenosine; arthritis; aryl hydrocarbon reductase; bifidobacilli; histamine; inflammatory bowel; lactobacilli; metabolomics; microbiome; short-chain fatty acid.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / microbiology*
  • Autoimmune Diseases / therapy
  • Fatty Acids, Volatile / metabolism
  • Gastrointestinal Microbiome / immunology
  • Humans
  • Inflammation / microbiology
  • Inflammatory Bowel Diseases / immunology
  • Inflammatory Bowel Diseases / microbiology*
  • Inflammatory Bowel Diseases / therapy
  • Intestines / immunology
  • Intestines / microbiology
  • Nucleosides / metabolism
  • Probiotics / pharmacology*
  • Receptors, Aryl Hydrocarbon / metabolism
  • Receptors, Histamine H2 / metabolism
  • Rheumatic Diseases / immunology
  • Rheumatic Diseases / microbiology*
  • Rheumatic Diseases / therapy
  • Tryptophan / metabolism


  • Fatty Acids, Volatile
  • Nucleosides
  • Receptors, Aryl Hydrocarbon
  • Receptors, Histamine H2
  • Tryptophan