The authors examined serum antiglycolipid antibodies in 445 patients with G
uillain-Barre syndrome (GBS). Among them, nine had anti-GD1b IgG antibodies
with no reactivity to other glycolipids tested. All those patients had sen
sory disturbance, and none had the primary axonal form. Anti-GD1b IgG antib
odies may bind to primary sensory neurons and paranodal myelin, where GD1b
is localized, and be involved in the pathogenesis of sensory disturbance an
d demyelination. However, more study is needed to substantiate the roles of
anti-GD1b IgG antibodies.