Aberrant glycosylation of IgA from patients with IgA nephropathy
✍ Scribed by Dimitra Baharaki; Maryvonne Dueymes; Régine Perrichot; Christelle Basset; Rozenn Corre; Jacques Cledes; Pierre Youinou
- Publisher
- Springer US
- Year
- 1996
- Tongue
- English
- Weight
- 726 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1573-4986
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📜 SIMILAR VOLUMES
The mechanism of mesangial IgA deposition is poorly understood in IgA nephropathy (IgAN). Abnormal glycosylation of carbohydrate moieties in the hinge region of the IgA molecule has recently attracted much attention. In this report, we studied galactosylation and sialylation profiles in κand λ-IgA 1
IgA nephropathy (IgAN) is the most common form of chronic glomerulonephritis. Although glomerular deposition of complement components is well known, the evidence of serological complement activation in IgAN is inconclusive. We hypothesized that serum levels of complement components and regulatory pr
## Abstract Diagnostic analysis of clinical markers including serum IgA levels and serum IgA/C3 ratio in patients with IgA nephropathy is described. One hundred patients with IgA nephropathy (IgA nephropathy group) and 100 patients with other primary glomerular diseases (non‐IgA nephropathy group)
The production of hydrogen peroxide (H202) by neutrophilic polymorphonuclear leukocytes (PMN) after stimulation and the infiltration of PMN in glomeruli were determined in 20 patients with primary IgA nephropathy. The H202 production of PMN after the stimulation was measured with a spectrophotometer