Impaired B Cell Expression of the Inhibitory Fcγ Receptor IIB in Myasthenia Gravis.

Keller CW, Chuquisana O, Derdelinckx J, Gross CC, Berger K, Robinson J, Nimmerjahn F, Wiendl H, Willcox N, Lünemann JD

Research article (journal) | Peer reviewed

Abstract

Myasthenia gravis (MG) is an autoimmune disease in which pathogenic immunoglobulin G antibodies bind to acetylcholine receptors (or to functionally related molecules at the neuromuscular junction). B cell expression of the inhibitory immunoglobulin G receptor, Fc-gamma receptor (FcγR) IIB, maintains peripheral immune tolerance, and its absence renders B cells hyperresponsive to autoantigen. Here, we report that FcγRIIB expression levels are substantially reduced in B lineage cells derived from immunotherapy-naïve patients with acetylcholine receptor antibody-positive early-onset MG. In contrast, genetic variants associated with impaired FcγRIIB expression are not enriched in MG, indicating post-transcriptional dysregulation. FcγR-targeted therapies could have therapeutic benefits in MG. ANN NEUROL 2022.

Details about the publication

JournalAnnals of Neurology
Statusaccepted / in press (not yet published)
Release year2022 (12/09/2022)
Language in which the publication is writtenEnglish
DOI10.1002/ana.26507
KeywordsMyasthenia gravis (MG); immunoglobulin G antibodies; acetylcholine receptors; Fc-gamma receptor (FcγR) IIB

Authors from the University of Münster

Groß, Catharina
Department for Neurology
Keller, Christian Wolfgang
Department for Neurology
Lünemann, Jan
Department for Neurology
Wiendl, Heinz Siegfried
Department for Neurology