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Anti-alkaline phosphatase antibody positive myasthenia gravis.

作者信息

Konishi Tetsuro, Ohta Kiyoe, Shigemoto Kazuhiro, Ohta Mitsuhiro

机构信息

Department of Neurology, National Hospital Organization Utano National Hospital, 8, Ondoyama-cho, Narutaki, Ukyo-ku, Kyoto 616-8255, Japan.

出版信息

J Neurol Sci. 2007 Dec 15;263(1-2):89-93. doi: 10.1016/j.jns.2007.06.006. Epub 2007 Jul 12.

Abstract

Anti-alkaline phosphatase antibody (AP Ab) was specific in 9% of 249 anti-acetylcholine receptor (AChR) Ab-positive myasthenia gravis (MG) (SPMG) patients but not in patients with AChR Ab-negative MG (SNMG), other neurological and immunological diseases, or healthy volunteers. No cross-reactivity and no significant titer correlation were found between AP Ab and AChR Ab. We confirmed immunologically by radioimmunoassay and western blot analysis the presence of antibodies directed against AP. AP Ab-positive SPMG patients were characterized clinically as having female predominance and a more severe form of generalized MG than AP Ab-negative SPMG patients, and about half required artificial ventilation at maximum severity. AP Ab's pathogenic role in MG is yet unclarified, but our findings show AP to be a novel antigen among the various autoantigens present in MG patients and in whom AP Ab may modify clinical symptoms.

摘要

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