No strong HLA association with MOG antibody disease in the UK population

被引:21
作者
Grant-Peters, Melissa [1 ]
Passos, Giordani Rodrigues Dos [2 ,3 ,4 ]
Yeung, Hing-Yuen [1 ]
Jacob, Anu [5 ]
Huda, Saif [5 ]
Leite, Maria Isabel [2 ]
Dendrou, Calliope A. [1 ]
Palace, Jacqueline [2 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Wellcome Ctr Human Genet, Oxford OX3 7BN, England
[2] John Radcliffe Hosp, Dept Clin Neurol, Oxford OX3 9DS, England
[3] Pontifical Catholic Univ Rio Grande Porto Alegre, Brain Inst, Porto Alegre, RS, Brazil
[4] Pontifical Catholic Univ Rio Grande Porto Alegre, Dept Neurol, Porto Alegre, RS, Brazil
[5] NHS Fdn Trust, Walton Ctr, Liverpool, Merseyside, England
基金
英国惠康基金;
关键词
MULTIPLE-SCLEROSIS; OLIGODENDROCYTE; SPECTRUM;
D O I
10.1002/acn3.51378
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Improvements in assays for detecting serum antibodies against myelin oligo-dendrocyte glycoprotein (MOG) have led to the appreciation of MOG-antibody-associated disease (MOGAD) as a novel disorder. However, much remains unknown about its etiology. We performed human leukocyte antigen (HLA) analysis in 82 MOGAD patients of European ancestry in the UK population. No HLA class II associations were observed, thus questioning the mechanism of anti-MOG antibody generation. A weak protective association of HLA-C*03:04 was observed (OR = 0.26, 95% CI = 0.10-0.71, p(c) = 0.013), suggesting a need for continued efforts to better understand MOGAD genetics and pathophysiology.
引用
收藏
页码:1502 / 1507
页数:6
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