Novel autoantigens recognized by CSF IgG from Hashimoto's encephalitis revealed by a proteomic approach

被引:48
作者
Gini, Beatrice [1 ]
Lovato, Laura [1 ]
Cianti, Riccardo [2 ]
Cecotti, Laura [3 ]
Marconi, Silvia [1 ]
Anghileri, Elena [1 ]
Armini, Alessandro [2 ]
Moretto, Giuseppe [4 ]
Bini, Luca
Ferracci, Franco [3 ]
Bonetti, Bruno [1 ]
机构
[1] Univ Verona, Dept Neurol Sci & Vis, Sect Neurol, I-37134 Verona, Italy
[2] Hosp S Martino, Belhmo, Italy
[3] Univ Siena, Dept Mol Biol, Siena, Italy
[4] Azienda Osped, Verona, Italy
关键词
Hashimoto's encephalitis; proteomics; autoantibodies; DDAHI; AKRIAI;
D O I
10.1016/j.jneuroim.2008.02.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To identify the target of IgG autoimmune response in Hashimoto's encephalopathy (HE), we studied the binding of IgG present in serum and cerebro-spinal fluid (CSF) from six patients with HE and 15 controls to human central nervous system (CNS) white matter antigens by 2D-PAGE and immunoblotting and by immunohistochemistry. We found that CSF IgG from HE patients specifically recognized 3 spots, which were identified as dimethylargininase-I (DDAHI) and aldehyde reductase-I (AKRIAI). DDAHI was present in two isoforms recognized respectively by five and four HE patients; immunohistochemistry with anti-DDAHI antiserum depicted endothelial cells in normal human CNS. AKRIAI was recognized by three HE CSF and this enzyme was widely distributed on neurons and endothelia by immunohistochemistry. IgG from HE CSF immunostained both neuronal and endothelial cells in mouse CNS. The presence of these autoantibodies selectively in the CSF of HE patients may have important diagnostic and pathogenetic implications, since the autoimmune response to these enzymes may lead to vascular and/or neuronal damage, two major mechanisms involved in the pathogenesis of HE. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:153 / 158
页数:6
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