The microbiome-systemic diseases connection

Research output: Contribution to journalReview articlepeer-review

52 Citations (Scopus)

Abstract

The human microbiome consists of all microorganisms occupying the skin, mucous membranes and intestinal tract of the human body. The contact of the mucosal immune system with the human microbiome is a balanced interplay between defence mechanisms of the immune system and symbiotic or pathogenic microbial factors, such as microbial antigens and metabolites. In systemic autoimmune diseases (SADs) such as rheumatoid arthritis, systemic lupus erythematosus and Sjogren's syndrome, the immune system is deranged to a chronic inflammatory state and autoantibodies are an important hallmark. Specific bacteria and/or a dysbiosis in the human microbiome can lead to local mucosal inflammation and increased intestinal permeability. Proinflammatory lymphocytes and cytokines can spread to the systemic circulation and increase the risk of inflammation at distant anatomical sites, such as the joints or salivary glands. Increased intestinal permeability increases antigen exposure and the risk of autoantibody production. If the human microbiome indeed plays such a critical role in SADs, this finding holds a great promise for new therapeutic strategies, such as diet interventions and probiotics and prebiotics. This review provides a background on the human microbiome and mucosal immunity in the gut and oral cavity and gives a summary of the current knowledge on the microbiome-SADs connection.

Original languageEnglish
Pages (from-to)719-734
Number of pages16
JournalOral diseases
Volume22
Issue number8
DOIs
Publication statusPublished - Nov-2016

Keywords

  • autoinflammatory diseases
  • inflammatory diseases
  • bacteria
  • microbiology
  • immunopathology
  • pathogenesis
  • rheumatology
  • immunology
  • autoimmune disease
  • PRIMARY SJOGRENS-SYNDROME
  • AUTOIMMUNE RHEUMATIC-DISEASES
  • EPSTEIN-BARR-VIRUS
  • POLYMERIC IMMUNOGLOBULIN RECEPTOR
  • SEGMENTED FILAMENTOUS BACTERIA
  • INFLAMMATORY-BOWEL-DISEASE
  • INFANT GUT MICROBIOME
  • B-CELL HYPERACTIVITY
  • LUPUS-ERYTHEMATOSUS
  • CLASSIFICATION CRITERIA

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