The Immune Tolerance Role of the HMGB1-RAGE Axis

The disruption of the immune tolerance induces autoimmunity such as systemic lupus erythematosus and vasculitis. A chromatin-binding non-histone protein, high mobility group box 1 (HMGB1), is released from the nucleus to the extracellular milieu in particular environments such as autoimmunity, sepsis and hypoxia. Extracellular HMGB1 engages pattern recognition receptors, including Toll-like receptors (TLRs) and the receptor for advanced glycation endproducts (RAGE). While the HMGB1-RAGE axis drives inflammation in various diseases, recent studies also focus on the anti-inflammatory effects of HMGB1 and RAGE. This review discusses current perspectives on HMGB1 and RAGE's roles in controlling inflammation and immune tolerance. We also suggest how RAGE heterodimers responding microenvironments functions in immune responses.

Automated summary

The review examines the roles of HMGB1 and RAGE in controlling inflammation and immune tolerance, highlighting the dual effects of the HMGB1-RAGE axis in driving inflammation and its potential anti-inflammatory effects. The discussion also touches on how RAGE heterodimers respond to microenvironments in immune responses.