重症肌无力
受体
乙酰胆碱受体
抗体
免疫学
免疫疗法
免疫系统
抑制性突触后电位
自身免疫性疾病
神经肌肉接头
乙酰胆碱
生物
化学
医学
内分泌学
内科学
神经科学
作者
Christian W. Keller,Omar Chuquisana,Judith Derdelinckx,Catharina C. Groß,Klaus Peter Berger,James Robinson,Falk Nimmerjahn,Heinz Wiendl,Nick Willcox,Jan D. Lünemann
摘要
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;92:1046–1051
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