期刊
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
卷 91, 期 7, 页码 733-739出版社
BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2019-322115
关键词
-
资金
- National Natural Science Foundation of China [81 971 140, 81870953]
- Natural Science Foundation of Guangdong Province, China [2017A030313853, 2014A030312001]
Objective Myelin oligodendrocyte glycoprotein-associated disorders (MOGADs) are a rare new neurological autoimmune disease with unclear pathogenesis. Since a linkage of the disease to the human leucocyte antigen (HLA) has not been shown, we here investigated whether MOGAD is associated with the HLA locus. Methods HLA genotypes of 95 patients with MOGADs, assessed between 2016 and 2018 from three academic centres, were compared with 481 healthy Chinese Han individuals. Patients with MOGADs included 51 paediatric-onset and 44 adult-onset cases. All patients were seropositive for IgG targeting the myelin oligodendrocyte glycoprotein (MOG). Results Paediatric-onset MOGAD was associated with theDQB1*05:02-DRB1*16:02alleles (OR=2.43; OR=3.28) or haplotype (OR=2.84) ofHLAclass II genes. The prevalence of these genotypes in patients with paediatric-onset MOGAD was significantly higher than healthy controls (p(adj)=0.0154; p(adj)=0.0221; p(adj)=0.0331). By contrast, adult-onset MOGAD was not associated with any HLA genotype. Clinically, patients with theDQB1*05:02-DRB1*16:02haplotype exhibited significantly higher expanded disability status scale scores at onset (p=0.004) and were more likely to undergo a disease relapse (p=0.030). HLA-peptide binding prediction algorithms and computational docking analysis provided supporting evidence for the close relationship between the MOG peptide subunit andDQB1*05:02allele. In vitro results indicated that site-specific mutations of the predicted target sequence reduced the antigen-antibody binding, especially in the paediatric-onset group withDQB1*05:02allele. Conclusions This study demonstrates a possible association between specificHLAclass II alleles and paediatric-onset MOGAD, providing evidence for the conjecture that different aetiology and pathogenesis likely underlie paediatric-onset and adult-onset cases of MOGAD.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据