Published online Jan 6, 2023. doi: 10.12998/wjcc.v11.i1.1
Peer-review started: September 26, 2022
First decision: October 18, 2022
Revised: October 29, 2022
Accepted: December 15, 2022
Article in press: December 15, 2022
Published online: January 6, 2023
Processing time: 101 Days and 0.5 Hours
The central nervous system (CNS) is a reservoir of immune privilege. Specialized immune glial cells are responsible for maintenance and defense against foreign invaders. The blood–brain barrier (BBB) prevents detrimental pathogens and potentially overreactive immune cells from entering the periphery. When the double-edged neuroinflammatory response is overloaded, it no longer has the protective function of promoting neuroregeneration. Notably, microbiota and its derivatives may emerge as pathogen-associated molecular patterns of brain pathology, causing microbiome–gut–brain axis dysregulation from the bottom-up. When dysbiosis of the gastrointestinal flora leads to subsequent alterations in BBB permeability, peripheral immune cells are recruited to the brain. This results in amplification of neuroinflammatory circuits in the brain, which eventually leads to specific neurological disorders. Aggressive treatment strategies for gastro
Core Tip: Neurological disorders are increasingly diagnosed globally owing to the disruption of the gut-brain axis. The impact of dysbiosis on the gut microbiota often plays a crucial role in disease pathogenesis. A thorough understanding of this complex relationship is essential for the development of new management strategies against various neurological disorders.