Autoantibodies to Low-Density Lipoprotein Receptor-Related Protein 4 in Myasthenia Gravis

被引:332
|
作者
Higuchi, Osamu
Hamuro, Johko
Motomura, Masakatsu [2 ]
Yamanashi, Yuji [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Canc Biol, Div Genet,Minato Ku, Tokyo 1088639, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Dept Internal Med 1, Nagasaki 852, Japan
关键词
ACETYLCHOLINE-RECEPTORS; NEUROMUSCULAR-JUNCTION; ANTIBODIES; MUSK; AGRIN; LRP4;
D O I
10.1002/ana.22312
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Myasthenia gravis (MG) is an autoimmune disease of the neuromuscular junction, where acetylcholine receptor (AChR), muscle-specific kinase (MuSK), and low-density lipoprotein (LDL) receptor-related protein 4 (Lrp4) are essential. About 80% and 0% to 10% of patients with generalized MG have autoantibodies to AChR and MuSK, respectively, but pathogenic factors are elusive in others. Here we show that a proportion of AChR antibody-negative patients have autoantibodies to Lrp4. These antibodies inhibit binding of Lrp4 to its ligand and predominantly belong to the immunoglobulin G1 (IgG1) subclass, a complement activator. These findings together indicate the involvement of Lrp4 antibodies in the pathogenesis of AChR antibody-negative MG. ANN NEUROL 2011;69:418-422
引用
收藏
页码:418 / 422
页数:5
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