PT  - JOURNAL ARTICLE
AU  - Xiaobo Sun
AU  - Wei Qiu
AU  - Jingqi Wang
AU  - Shisi Wang
AU  - Yuge Wang
AU  - Xiaonan Zhong
AU  - Chunxin Liu
AU  - Chunping Cui
AU  - Hai Hong
AU  - Hui Yang
AU  - Xiao-Jing Li
AU  - Zhengqi Lu
AU  - Xueqiang Hu
AU  - Allan G Kermode
AU  - Lisheng Peng
TI  - Myelin oligodendrocyte glycoprotein-associated disorders are associated with HLA subtypes in a Chinese paediatric-onset cohort
AID  - 10.1136/jnnp-2019-322115
DP  - 2020 May 19
TA  - Journal of Neurology, Neurosurgery & Psychiatry
PG  - jnnp-2019-322115
4099  - http://jnnp.bmj.com/content/early/2020/05/18/jnnp-2019-322115.short
4100  - http://jnnp.bmj.com/content/early/2020/05/18/jnnp-2019-322115.full
AB  - 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 the DQB1*05:02–DRB1*16:02 alleles (OR=2.43; OR=3.28) or haplotype (OR=2.84) of HLA class II genes. The prevalence of these genotypes in patients with paediatric-onset MOGAD was significantly higher than healthy controls (padj=0.0154; padj=0.0221; padj=0.0331). By contrast, adult-onset MOGAD was not associated with any HLA genotype. Clinically, patients with the DQB1*05:02–DRB1*16:02 haplotype 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 and DQB1*05:02 allele. In vitro results indicated that site-specific mutations of the predicted target sequence reduced the antigen–antibody binding, especially in the paediatric-onset group with DQB1*05:02 allele.Conclusions This study demonstrates a possible association between specific HLA class 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.