Gut microbiota in children and altered profiles in juvenile idiopathic arthritis

Carlotta De Filippo1, Monica Di Paola2, Teresa Giani3

  • 1Institute of Biology and Agrarian Biotechnology (IBBA), National Research Council (CNR), Via Moruzzi 1, 56124 Pisa, Italy.

Journal of Autoimmunity
|January 15, 2019
PubMed

Insights

Gut microbiota and its metabolites are crucial for immune system development. Dysbiosis, or an imbalance in gut bacteria, is linked to Juvenile Idiopathic Arthritis (JIA) and inflammation.

Area of Science:

  • Microbiology
  • Immunology
  • Gastroenterology

Background:

  • The gut microbiota is essential for intestinal homeostasis and immune system development, particularly in childhood.
  • Microbial metabolites like Short Chain Fatty Acids (SCFAs) play a vital role in immune system training and immunotolerance.
  • Gut dysbiosis is implicated in rheumatic diseases, potentially leading to increased gut permeability, immune imbalance, and inflammation.

Purpose of the Study:

  • To explore the role of gut dysbiosis as a potential pathogenetic factor in Juvenile Idiopathic Arthritis (JIA).
  • To summarize existing studies on microbial profiles in JIA patients.

Main Methods:

  • Review of studies investigating the gut microbiota composition in JIA patients.
  • Comparison of microbial profiles between JIA patients and healthy subjects.

Main Results:

  • JIA patients exhibit distinct microbial profiles compared to healthy individuals.
  • A depletion of microbial biodiversity and the presence of pro-arthritogenic microbial profiles are observed in JIA patients.
  • These microbial alterations suggest a potential link between gut dysbiosis and JIA pathogenesis.

Conclusions:

  • Gut dysbiosis, characterized by altered microbial composition and reduced biodiversity, is increasingly recognized as a significant factor in JIA pathogenesis.
  • Further research is necessary to fully elucidate the intricate relationship between the gut microbiota and JIA.
  • Targeting gut microbiota modulation may offer future therapeutic strategies for JIA.

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