Antibodies to AMPA receptors in Rasmussen's encephalitis

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
Anjan NibberBethan Lang

Abstract

Rasmussen's encephalitis is a rare progressive childhood disorder characterized by frequent severe seizures, hemiparesis, encephalitis and mental deterioration, and associated with severe unilateral neuroinflammation. Autoantibodies, particularly to the GluA3 subtype of the alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propinonic acid receptor (AMPAR) were reported in the 1990s but not always confirmed. To explore further, sera from 52 patients with Rasmussen's encephalitis were tested by cell-based assays for antibodies to AMPAR GluA1/2/3, N-methyl-d-aspartate (NMDA NR1/2b), γ-aminobutyric acid type A and B (GABAAR α1/γ2/β2 and GABABR b1/b2) receptors, for potassium channel complex proteins, and for binding to live cortical and hippocampal neuronal cultures. Two patients' sera (3.8%) bound to HEK cells co-transfected with the GluA2 and GluA3 subunits. One additional patient had a low level of VGKC-complex antibodies. These three, and seven additional, sera bound to hippocampal cultures. No other antibodies were detected. Thus, despite the rarity of GluA2/3 antibodies, 10 patients (19.2%) had evidence of antibodies to neuronal antigens. Whether these antibodies play a primary role in RE, or appear secondary to the neuro-inflammato...Continue Reading

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Citations

Jan 7, 2017·Journal of Child Neurology·Sukhvir Wright, Angela Vincent
Mar 31, 2017·PloS One·Caleigh M AzumayaTerunaga Nakagawa
Feb 25, 2017·Current Opinion in Neurology·Marianna Spatola, Josep Dalmau
Feb 26, 2019·F1000Research·Priya SharmaRobert Greenwood
Jul 10, 2019·Epilepsia·Alberto VogrigJérome Honnorat
Dec 15, 2020·Epilepsia·Tracie Huey-Lin TanMastura Monif
Aug 10, 2020·Seizure : the Journal of the British Epilepsy Association·A OrsiniP Striano

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