ISSN: E-2314-7326
P-2314-7334

Neuroinfektiöse Krankheiten

Offener Zugang

Unsere Gruppe organisiert über 3000 globale Konferenzreihen Jährliche Veranstaltungen in den USA, Europa und anderen Ländern. Asien mit Unterstützung von 1000 weiteren wissenschaftlichen Gesellschaften und veröffentlicht über 700 Open Access Zeitschriften, die über 50.000 bedeutende Persönlichkeiten und renommierte Wissenschaftler als Redaktionsmitglieder enthalten.

Open-Access-Zeitschriften gewinnen mehr Leser und Zitierungen
700 Zeitschriften und 15.000.000 Leser Jede Zeitschrift erhält mehr als 25.000 Leser

Abstrakt

Pathogenic Pathways in Neuronal Surface Autoantibody-Mediated Encephalitis

Arun J. Gill

Neuronal surface autoantibody-mediated encephalitis (NSAME) is a complex and rapidly emerging field of neuroimmunology characterized by immune-mediated attacks on neuronal cell surface antigens. This abstract provides an overview of the pathogenic pathways underlying NSAME, summarizing key mechanisms and factors contributing to disease development. NSAME is associated with a wide spectrum of clinical manifestations, often presenting with a range of neurological and psychiatric symptoms. Central to the pathogenesis of NSAME are autoantibodies targeting specific neuronal surface proteins, such as NMDA receptors, LGI1, CASPR2, and GABA (B) receptors, among others. These autoantibodies disrupt synaptic transmission, induce receptor internalization, and trigger inflammatory responses in the central nervous system. Additionally, genetic predisposition, environmental triggers, and dysregulated immune responses play pivotal roles in disease initiation and progression. This abstract aims to elucidate the intricate interplay between autoimmunity, neuroinflammation, and neuronal dysfunction in NSAME, shedding light on potential therapeutic strategies for this challenging neurological disorder. Understanding these pathogenic pathways is critical for advancing the diagnosis, treatment, and management of NSAME and improving the quality of life for affected individuals.