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神经退行性疾病巴滕病中谷氨酸脱羧酶的自身免疫反应

Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.

作者信息

Ramirez-Montealegre D, Chattopadhyay S, Curran T M, Wasserfall C, Pritchard L, Schatz D, Petitto J, Hopkins D, She J-X, Rothberg P G, Atkinson M, Pearce D A

机构信息

Aab Institute of Biomedical Sciences, Center for Aging and Developmental Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

出版信息

Neurology. 2005 Feb 22;64(4):743-5. doi: 10.1212/01.WNL.0000151973.08426.7E.

Abstract

The pathogenic mechanisms underlying Batten disease are unclear. Patients uniformly possess autoantibodies against glutamic acid decarboxylase (GAD) that are predominantly reactive with a region of GAD (amino acids 1 to 20) distinct from subjects with autoimmune type 1 diabetes or stiff-person syndrome. Batten patients did not possess autoantibodies against other type 1 diabetes-associated autoantigens and human leukocyte antigen genotypes revealed no specific associations with this disease.

摘要

巴滕病的致病机制尚不清楚。患者均具有针对谷氨酸脱羧酶(GAD)的自身抗体,这些抗体主要与GAD的一个区域(氨基酸1至20)发生反应,该区域与1型自身免疫性糖尿病或僵人综合征患者不同。巴滕病患者不具有针对其他1型糖尿病相关自身抗原的自身抗体,并且人类白细胞抗原基因型与该疾病无特定关联。

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