Research projects
SYNABS - Synaptic pathology in autoimmune encephalitis
Speaker: Prof. Dr. Christian Geis
DFG (FOR 3004) 2020-2023
The discovery of autoantibodies against synaptic antigens in the central nervous system (CNS) in patients with severe neuropsychiatric disorders was a breakthrough in neurology. As of today, more than 15 target molecules have been identified to which specific autoantibodies are directed each defining a subtype of disease. Importantly, these target antigens are all part of central synapses and are comprised of ionotropic and metabotrobic receptors as well as adhesion and transsynaptic signaling molecules. This novel entity of CNS disorders has been termed “autoimmune encephalitis”. The underlying pathophysiology including the molecular interactions and the often detrimental impact of the antibodies on neurons, synapses and consequently on network function are only partly understood. As a consequence, target-specific therapies are currently not available. The DFG Research Unit “Synaptic pathology in autoimmune encephalitis” (SYNABS) brings together clinician scientists in the field of antibody-mediated immunological disorders with basic scientists in the field of neurophysiology, molecular neurobiology, and neuroimmunology collectively investigating autoantibody-mediated pathology in the CNS. The aim of SYNABS is to elucidate the pathophysiology of autoimmune encephalitis in which autoantibodies are directed at synaptic targets.
Subprojects the Jena neurology is involved:
P1: Effects of human monoclonal anti-GluN1 autoantibodies on NMDA receptor channel function
Principal investigator: Prof. Dr. Christian Geis
P6: Effects of GABAB receptor antibodies on neuronal signalling and hippocampal function
Principal investigator: Prof. Dr. Christian Geis
P7: Developmental and synaptic defects caused by transplacental transmission of NMDA receptor antibodies
Principal investigator: Prof. Dr. Knut Kirmse