scispace - formally typeset
Journal ArticleDOI

Gangliosides GM1 and GD1b are antigens for IgM M-protein in a patient with motor neuron disease.

Reads0
Chats0
TLDR
A patient with an IgM M-protein and lower motor neuron disease was studied to identify the antigens to which the M- protein bound, indicating reactivity to the galactosyl(beta 1-3)N-acetylgalactosaminyl moiety shared by GM1, GD1b, and asialo-GM1.
Abstract
We studied a patient with an IgM M-protein and lower motor neuron disease to identify the antigens to which the M-protein bound. Gangliosides from peripheral nerve and spinal cord were separated by high-performance thin-layer chromatography and immunostained with the patient's serum. The serum IgM immunostained two gangliosides identified as GM1 and GD1b, and immunostaining was specific for the M-protein light chain type. IgM-binding to the two gangliosides was detectable by ELISA at serum dilutions of greater than 1:10,000, and the M-protein was selectively immunoabsorbed by liposomes containing GM1 or GD1b. The IgM M-protein also bound to asialo-GM1, indicating reactivity to the galactosyl(beta 1-3)N-acetylgalactosaminyl moiety shared by GM1, GD1b, and asialo-GM1.

read more

Citations
More filters
Journal ArticleDOI

Global Epidemiology of Campylobacter Infection

TL;DR: Overall, campylobacteriosis is still one of the most important infectious diseases that is likely to challenge global health in the years to come.
Journal ArticleDOI

Peripheral neuropathies and anti-glycolipid antibodies.

TL;DR: This review charts the progress of anti-glycolipid antibodies in neuropathy, from their original discovery 20 years ago in immunoglobulin M paraproteinaemic neuropathy through to current discoveries mapping their relationship to subtypes of Guillain-Barré syndrome.
Journal ArticleDOI

Serum anti‐GQ1b IgG antibody is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain‐Barré syndrome: Clinical and immunohistochemical studies

TL;DR: It is concluded that serum IgG antibody against GQ1b is very closely associated with acute postinfectious ophthalmoplegia in MFS and GBS and with other neurologic or non-neurologic disorders.
Journal ArticleDOI

A treatable multifocal motor neuropathy with antibodies to GM1 ganglioside.

TL;DR: 2 patients with a treatable, immune‐mediated motor polyneuropathy associated with antibodies to defined neural antigens, initially diagnosed as having lower motor neuron forms of amyotrophic lateral sclerosis are reported.
Journal ArticleDOI

Waldenström’s Macroglobulinemia: Clinical Features, Complications, and Management

TL;DR: Preliminary evidence suggests that anti-CD20 monoclonal antibody may be active in about 30% of previously treated patients and that high-dose therapy with autologous stem-cell rescue is effective in most patients, including some with resistance to nucleoside analogs.
Related Papers (5)