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Updated: Jun 13, 2026

Antibody Binding Specificity for Kappa (Vκ) Light Chain-containing Human (IgM) Antibodies: Polysialic Acid (PSA) Attached to NCAM as a Case Study
Published on: June 29, 2016
[Miller-Fisher syndrome associated with monoclonal IgG lambda antibodies against ganglioside GQ1b]
Christiane Caudie1, Emmeline Lagrange
1Service de Neurobiologie, Centre de Biologie et de Pathologie Est, Hôpitaux de Lyon, Bron, Pôle de Neurologie, Centre de Référence des Maladies Rares Neuromusculaires, CHU de Grenoble. christiane.caudie@chu-lyon.fr
Abstract:
We report a case of a 68-year-old man with classical triad, ophthalmoplegia, ataxia and areflexia in uncommon context. Our patient presented initial symptoms during radiation therapy for prostate cancer. After elimination of brainstem stroke and carcinomatous meningitidis by his general physician, he was referred with a provisional diagnosis of Miller-Fisher syndrome (MFS). The main characteristics of this case of MFS were uncommon: antecedent illness of urinary tract infections by Pseudomonas aeruginosa, presence of high titres of IgG antibodies directed against Mycoplasma pneumoniae, CSF pleocytosis and intrathecal IgG synthesis, serum and CSF monoclonal IgG in a monoclonal gammopathy of undetermined significance (MGUS). The serum and CSF immunological marker of MFS was a monoclonal IgG antibody targeting the ganglioside GQ1b with abundant expression on oculomotor nerves.
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