Probiotics and Prebiotics for the Amelioration of Type 1 Diabetes: Present and Future Perspectives.
Sidharth Prasad MishraShaohua WangRavinder NagpalBrandi MillerRia SinghSubhash TaraphderHariom YadavPublished in: Microorganisms (2019)
Type 1-diabetes (T1D) is an autoimmune disease characterized by immune-mediated destruction of pancreatic beta (β)-cells. Genetic and environmental interactions play an important role in immune system malfunction by priming an aggressive adaptive immune response against β-cells. The microbes inhabiting the human intestine closely interact with the enteric mucosal immune system. Gut microbiota colonization and immune system maturation occur in parallel during early years of life; hence, perturbations in the gut microbiota can impair the functions of immune cells and vice-versa. Abnormal gut microbiota perturbations (dysbiosis) are often detected in T1D subjects, particularly those diagnosed as multiple-autoantibody-positive as a result of an aggressive and adverse immunoresponse. The pathogenesis of T1D involves activation of self-reactive T-cells, resulting in the destruction of β-cells by CD8⁺ T-lymphocytes. It is also becoming clear that gut microbes interact closely with T-cells. The amelioration of gut dysbiosis using specific probiotics and prebiotics has been found to be associated with decline in the autoimmune response (with diminished inflammation) and gut integrity (through increased expression of tight-junction proteins in the intestinal epithelium). This review discusses the potential interactions between gut microbiota and immune mechanisms that are involved in the progression of T1D and contemplates the potential effects and prospects of gut microbiota modulators, including probiotic and prebiotic interventions, in the amelioration of T1D pathology, in both human and animal models.
Keyphrases
- induced apoptosis
- type diabetes
- cell cycle arrest
- endothelial cells
- immune response
- oxidative stress
- multiple sclerosis
- endoplasmic reticulum stress
- emergency department
- small molecule
- poor prognosis
- genome wide
- cardiovascular disease
- metabolic syndrome
- climate change
- induced pluripotent stem cells
- dna methylation
- copy number
- risk assessment
- inflammatory response
- insulin resistance
- long non coding rna
- weight loss