Abstract |
Immunoglobulin A nephropathy (IgAN), characterized by predominant or exclusive deposition of IgA1 in glomerular mesangium, is the most common primary glomerulonephritis worldwide. At present, the treatment is always limited due to the incomplete understanding of the pathogenesis of IgAN. Mesangial deposited IgA1 is the common final pathway leading to glomerulonephritis and renal injury. IgA1 protease, a proteolytic enzyme with strict substrate specificity for human IgA1, may be an effective therapeutic candidate for IgAN by removing the mesangial deposited IgA1.
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Authors | Lin-Shen Xie, Jun Huang, Wei Qin, Jun-Ming Fan |
Journal | Nephrology (Carlton, Vic.)
(Nephrology (Carlton))
Vol. 15
Issue 5
Pg. 584-6
(Aug 2010)
ISSN: 1440-1797 [Electronic] Australia |
PMID | 20649880
(Publication Type: Journal Article)
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Chemical References |
- Immunoglobulin A
- Protease Inhibitors
- Serine Endopeptidases
- IgA-specific serine endopeptidase
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Topics |
- Glomerular Mesangium
(drug effects, enzymology, immunology)
- Glomerulonephritis, IGA
(drug therapy, enzymology, immunology)
- Humans
- Immunoglobulin A
(metabolism)
- Protease Inhibitors
(therapeutic use)
- Serine Endopeptidases
(metabolism)
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