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Ganglionic acetylcholine receptor autoantibodies in patients with autoimmune diseases including primary biliary cirrhosis
Authors:Yasuhiro Maeda  Osamu Higuchi  Hideki Nakamura  Atsumasa Komori  Kiyoshi Migita
Affiliation:1. Department of Clinical Research,;2. Department of Neurology, National Hospital Organization Nagasaki Kawatana Medical Center, Nagasaki, Japan,;3. Department of Neuroimmunology,;4. Department of Clinical Research,;5. Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan,;6. Department of Hepatology, National Hospital Organization Nagasaki Medical Center, Nagasaki, Japan,
Abstract:Objectives: Autonomic dysfunction is closely associated with autoimmune diseases (AID) including primary biliary cirrhosis (PBC). The objective of this study was to determine the prevalence of anti-ganglionic (nicotinic) acetylcholine receptor (gAChR) antibodies in patients with AID.

Methods: We determined the presence of gAChR antibodies in serum samples from 146 patients (systemic lupus erythematosus [SLE]?=?32; rheumatoid arthritis [RA]?=?43; systemic sclerosis [SSc]?=?38; PBC=?33) without information regarding autonomic symptoms, as well as 34 patients with other neurological diseases [OND], and 73 healthy controls [HC]. We specifically analyzed sera for anti-gAChRα3 and -β4 antibodies using the luciferase immunoprecipitation system (LIPS) assay.

Results: LIPS assay detected anti-gAChRα3 and -β4 antibodies in the sera from patients with SLE (12.5%, 4/32), RA (18.6%, 8/43), SSc (13.2%, 5/38), PBC (9.1%, 3/33), OND (2.9%, 1/34), and HC (0.0%, 1/73). There were no significant correlations between the levels of anti-gAChRα3 and -β4 antibodies, and the total titers of autoantibodies in AID.

Conclusions: The results demonstrated a significant prevalence of anti-gAChR antibodies in patients with AID, which is independent of the production of other autoantibodies in patients with autoimmune diseases. These anti-gAChR antibodies could mediate the autonomic dysfunction involved in the autoimmune mechanisms of AID.
Keywords:Anti-ganglionic acetylcholine receptor antibodies  Primary biliary cirrhosis  Rheumatoid arthritis  Systemic lupus erythematosus  Systemic sclerosis
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