| Literature DB >> 29162406 |
Kunihiro Ichinose1, Kaname Ohyama2, Kaori Furukawa3, Osamu Higuchi4, Akihiro Mukaino5, Katsuya Satoh6, Shunya Nakane4, Toshimasa Shimizu3, Masataka Umeda3, Shoichi Fukui3, Ayako Nishino3, Hideki Nakajima5, Tomohiro Koga3, Shin-Ya Kawashiri3, Naoki Iwamoto3, Mami Tamai3, Hideki Nakamura3, Tomoki Origuchi6, Mari Yoshida7, Naotaka Kuroda2, Atsushi Kawakami3.
Abstract
Neuropsychiatric systemic lupus erythematosus (NPSLE) is often difficult to diagnose and distinguish from other diseases, because no NPSLE-specific antibodies have been identified. We developed a novel proteomic strategy for identifying and profiling antigens in immune complexes in the cerebrospinal fluid (CSF), and applied this strategy to 26 NPSLE patients. As controls, we also included 25 SLE patients without neuropsychiatric manifestations (SLE), 15 with relapsing remitting multiple sclerosis (MS) and 10 with normal pressure hydrocephalus (NPH). We identified immune complexes of suprabasin (SBSN) in the CSF of the NPSLE group. The titer of anti-SBSN antibodies was significantly higher in the CSF of the NPSLE group compared to those of the SLE, MS and NPH groups. Microarray data showed that the senescence and autophagy pathways were significantly changed in astrocytes exposed to anti-SBSN antibodies. Our findings indicate that SBSN could be a novel autoantibody for the evaluation of suspected NPSLE.Entities:
Keywords: Cerebrospinal fluid; Immune complexes; Neuropsychiatric systemic lupus erythematosus; Suprabasin
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Year: 2017 PMID: 29162406 DOI: 10.1016/j.clim.2017.11.006
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969