N-acetylgalactosaminyl GD1a is a target molecule for serum antibody in Guillain-Barré syndrome
✍ Scribed by Susumu Kusunoki; Atsuro Chiba; Kazuo Kon; Susumu Ando; Kazuko Arisawa; Asako Tate; Ichiro Kanazawa
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 649 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
✦ Synopsis
Serum antibodies against such major glycolipids as GMI, GDlb, and LM1 have been reported in patients in the acute phase of Guillain-Barre syndrome (GBS). Because minor unidentified glycolipids also may be targets of antibodies in GBS sera, we assayed serum antibody against a crude ganglioside fraction using thin-layer chromatogram immunostaining. Antibody activity was detected against a band that migrated just below GDla in 6 of the 50 patients with GBS tested. Antibody titer, as determined by enzyme-linked immunosorbent assay, decreased during the course of the disease. All 6 patients had suffered gastrointestinal infection before the neurological onset of GBS and showed low
📜 SIMILAR VOLUMES
## Abstract The first synthesis of ganglioside GalNAc‐GD1a, featuring efficient glycan assembly and a cyclic glucosyl ceramide as a versatile unit for ganglioside synthesis is described. Although ganglioside GalNAc‐GD1a was first found as a brain ganglioside, IgG autoantibodies to GalNAc‐GD1a were