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Antigen‐specific oligoclonal bands in cerebrospinal fluid and serum from patients with anti‐amphiphysin‐ and anti‐CV2/CRMP5 associated paraneoplastic neurological syndromes
Author(s) -
Stich O.,
Rauer S.
Publication year - 2007
Publication title -
european journal of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 124
eISSN - 1468-1331
pISSN - 1351-5101
DOI - 10.1111/j.1468-1331.2007.01802.x
Subject(s) - antigen , medicine , cerebrospinal fluid , antibody , serology , intrathecal , western blot , immunology , pathology , autoimmunity , isoelectric focusing , pathophysiology , chemistry , gene , biochemistry , surgery , enzyme
Using isoelectric focusing and affinity blotting employing paraneoplastic recombinant antigens, we investigated cerebrospinal fluid (CSF) and sera from three patients with positive anti‐CV2/CRMP5‐ and one patient with positive anti‐amphiphysin serology. CSF and sera were previously adjusted to total IgG concentrations of 20 mg/l. All patients suffered from paraneoplastic neurological syndromes (PNS) with predominant involvement of the central nervous system (CNS). Using affinity blot preloaded with paraneoplastic antigen, we detected in three of four patients more or stronger specific oligoclonal bands (OCB) in the CSF than in the corresponding serum, providing qualitative evidence of antigen specific intrathecal antibody synthesis. These results are in line with previous studies demonstrating specific OCB predominantly in CSF from patients with anti‐Hu‐, anti‐Yo‐ and anti‐Ri‐associated PNS, supporting the hypothesis of autoimmunity in the pathogenesis of PNS. One patient harboured extensive anti‐amphiphysin specific OCB, although OCB of total IgG could not be detected, indicating a higher sensitivity for detection of intrathecal antibody synthesis of the affinity blot preloaded with the paraneoplastic antigen, compared with investigation of total IgG OCB. These results could have implications concerning pathophysiological autoimmune aspects in other inflammatory diseases of CNS associated with total IgG OCB, provided that the target antigen is known.