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   <subfield code="a">Humoral Immunity Against Glutamic Acid Decarboxylase and Tyrosine Phosphatase IA-2 in Lambert-Eaton Myasthenic Syndrome</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Laurence Hermitte, Nicole Martin-Moutot, Jose Boucraut, Roselyne Barone, Catherine Atlan-Gepner, Micha¨el Seagar, Jean Pouget, Jean-Pierre Kleisbauer, Fran¸cois Couraud, Bernard Vialettes]</subfield>
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   <subfield code="a">Some β-cell-specific autoantigens also are present in the central nervous system. Furthermore, stiff man syndrome, an autoimmune neurological disease, is frequently associated with diabetes and shares with this one an anti-GAD and IA-2 humoral immunoreactivity. We wondered whether these autoantibodies could be found in other neurological diseases with a present or supposed autoimmune origin. So, anti-GAD65 (GAD65A) and anti-IA-2 (IA-2A) autoantibodies were assayed in various neurological diseases. There was a higher prevalence of such antibodies in Lambert-Eaton myasthenic syndrome (LEMS) (GAD65A, 35%; IA-2A, 21%; double positivity, 18%) compared to amyotrophic lateral sclerosis (18%, 12%, and 12%, respectively) and multiple sclerosis (10%, 3%, and 3%, respectively). In LEMS, the humoral reaction was more frequent and/or appeared earlier in the paraneoplastic forms. The detection of such autoantibodies in patients with small-cell lung carcinoma (SCLC) without LEMS suggests that these autoantigens, GAD65 and IA-2, could be produced by SCLC tissue.</subfield>
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