| Literature DB >> 12297304 |
Hirofumi Ochi1, Izumi Horiuchi, Norie Araki, Tosifusa Toda, Tomohiro Araki, Kaori Sato, Hiroyuki Murai, Manabu Osoegawa, Takeshi Yamada, Ken Okamura, Tomoaki Ogino, Kiyohisa Mizumoto, Hirohumi Yamashita, Hideyuki Saya, Jun-ichi Kira.
Abstract
Hashimoto's encephalopathy (HE) is a rare autoimmune disease associated with Hashimoto's thyroiditis (HT). To identify the HE-related autoantigens, we developed a human brain proteome map using two-dimensional electrophoresis and applied it to the immuno-screening of brain proteins that react with autoantibodies in HE patients. After sequential MALDI-TOF-MASS analysis, immuno-positive spots of 48 kDa (pI 7.3-7.8) detected from HE patient sera were identified as a novel autoimmuno-antigen, alpha-enolase, harboring several modifications. Specific high reactivities against human alpha-enolase were significant in HE patients with excellent corticosteroid sensitivity, whereas the patients with fair or poor sensitivity to the corticosteroid treatment showed less reactivities than cut-off level. Although a few HT patients showed faint reactions to alpha-enolase, 95% of HT patients, patients with other neurological disorders, and healthy subjects tested were all negative. These results suggest that the detection of anti-alpha-enolase antibody is useful for defining HE-related pathology, and this proteomic strategy is a powerful method for identifying autoantigens of various central nervous system diseases with unknown autoimmune etiologies.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12297304 DOI: 10.1016/s0014-5793(02)03307-0
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124