ausblenden:
Schlagwörter:
MYELIN BASIC-PROTEIN; T-CELL-RECEPTOR; CENTRAL-NERVOUS-SYSTEM;
MULTIPLE-SCLEROSIS PATIENTS; HUMAN GUT MICROBIOME; PARKINSONS-DISEASE;
DEMYELINATING DISEASE; TRANSGENIC MICE; ANTIBIOTIC USE; IMMUNE-SYSTEMImmunology;
Zusammenfassung:
T cells play a critical role in autoimmune diseases in the brain, particularly in multiple sclerosis (MS). Since T cells are normally prevented from crossing the blood-brain barrier (BBB), autoimmunity requires prior activation of naturally occurring autoreactive T cells in peripheral tissue. Recently, a critical role for the microbiota in this activation process has emerged. Here, we review the role of gut-associated lymphoid tissues (GALT) as a major site for the phenotypic changes that allow the migration of autoreactive T cells to the brain. Additionally, we examine the involvement of the microbiota in clinical MS as well as other brain disorders such as Parkinson's disease (PD), stroke, and psychiatric disorders.