ANTIBODIES TO FUCOGANGLIOSIDES IN NEUROLOGICAL DISEASES
Citation
N. Yuki et T. Ariga, ANTIBODIES TO FUCOGANGLIOSIDES IN NEUROLOGICAL DISEASES, Journal of the neurological sciences, 150(1), 1997, pp. 81-84
Categorie Soggetti
Neurosciences
SICI code
0022-510X(1997)150:1<81:ATFIND>2.0.ZU;2-F
Abstract
We examined serum antibodies to 4 species of fucogangliosides: fucosyl
-GM1, fucosyl-GD1b, alpha galactosyl (alpha fucosyl) GM1 and alpha gal
actosyl (alpha fucosyl) GD1b, in 329 patients with various neurologic
diseases, 32 patients with non-neurologic autoimmune diseases and 50 h
ealthy persons. Nine patients with Guillain-Barre syndrome, 2 with amy
otrophic lateral sclerosis and 2 with cerebral infarction had IgG anti
-fucosyl-GM1 antibody. Five patients with Guillain-Barre syndrome. 1 w
ith cerebral infarction and 1 normal control subject had IgM anti-fuco
syl-GM1 antibody, 3 of whom also had IgG anti-fucosyl-GM1 antibody. Si
xteen of 17 patients who had Ige or IgM antibody to fucosyl-GM1 showed
no sensory dysfunction. Yoshino et al. [J. Neurochem. 1993, 61: 658-6
63] speculated that anti-fucosyl-GM1 antibody functions in the develop
ment of sensory neuropathy, but our results do not support this. Two p
atients with sensory ataxic neuropathy had high IgM antibody titers to
fucosyl-GD1b and alpha galactosyl (alpha fucosyl) GD1b. These fucogan
gliosides maybe the target molecules for serum antibodies in some pati
ents with sensory ataxic neuropathy. (C) 1997 Elsevier Science B.V.