Obesity is associated with impaired immune function, characterized by inflammation, and leading to poor response to infection, impaired vaccine response, increased susceptibility to autoimmune disease, and increased risk of cancer and cancer mortality. Worse, there is evidence that weight loss alone may be insufficient to reverse the immune dysfunction caused by obesity. It is therefore critically important to identify alternative therapeutic approaches to decrease the negative effects of obesity-associated inflammation. In this article, we will review evidence that the antidiabetic drug metformin may be considered as a therapeutic agent for obesity-associated immune dysfunction. Metformin has immunomodulatory effects, stimulating or suppressing the immune response in both a cell-specific and disease-specific manner. Although the mechanism of action of metformin on the immune system remains to be fully elucidated, there is strong evidence that metformin enters select immune cells and disrupts electron transport, leading to both AMP-activated protein kinase (AMPK)-dependent and AMPK-independent effects on immune cell differentiation and cytokine production. These effects of metformin on immune cells have been shown to improve immune responses to infection, autoimmunity, and cancer.
Keyphrases
- weight loss
- insulin resistance
- immune response
- metabolic syndrome
- protein kinase
- oxidative stress
- high fat diet induced
- bariatric surgery
- type diabetes
- weight gain
- papillary thyroid
- roux en y gastric bypass
- squamous cell
- skeletal muscle
- gastric bypass
- multiple sclerosis
- emergency department
- adipose tissue
- single cell
- stem cells
- body mass index
- squamous cell carcinoma
- signaling pathway
- risk factors
- mesenchymal stem cells
- glycemic control