INTRAGLOMERULAR DEPOSITION OF INTACT CROSS-LINKED FIBRIN IN IGA NEPHROPATHY AND HENOCH-SCHONLEIN PURPURA NEPHRITIS

Citation
T. Ono et al., INTRAGLOMERULAR DEPOSITION OF INTACT CROSS-LINKED FIBRIN IN IGA NEPHROPATHY AND HENOCH-SCHONLEIN PURPURA NEPHRITIS, Nephron, 74(3), 1996, pp. 522-528
Citations number
15
Categorie Soggetti
Urology & Nephrology
Journal title
ISSN journal
00282766
Volume
74
Issue
3
Year of publication
1996
Pages
522 - 528
Database
ISI
SICI code
0028-2766(1996)74:3<522:IDOICF>2.0.ZU;2-A
Abstract
To investigate the significance of intraglomerular coagulation and fib rinolysis in IgA nephropathy (IgA-N) and Henoch-Schonlein purpura neph ritis (HSPN), the distribution of intact cross-linked fibrin (XFb) mod ulated by plasmin activity was examined in 25 patients with IgA-N and in 12 with HSPN. In addition to the conventional method detecting fibr in-related antigen (FRA) with an antibody against fibrinogen, the enha nced intensity of immunoreactivity of cross-linked FRA (XL-FRA) using the monoclonal antibody DD3B6/22 after plasmin exposure was evaluated to assess intraglomerular deposition of intact XFb. Also, intraglomeru lar invasion of macrophages was detected using the monoclonal antibody KP1 against CD68. Sixteen of a total of 37 specimens (43%) showed inc reased intensity of XL-FRA staining after plasmin treatment which is c onsidered to reflect the distribution of intact XFb. Increases in the intensity of XL-FRA staining were observed mainly in mesangium and par tially along glomerular capillary loops and also in a few cases in the crescents. The incidence (67%) of increases in XL-FRA staining after plasmin exposure in HSPN specimens was significantly higher than that in IgA-N specimens (32%; p < 0.05). In the group positive for XL-FRA a fter plasmin exposure, the numbers of macrophages per glomerulus were significantly higher (n = 15; mean +/- SD = 1.6 +/- 0.9) than in the n egative group (n = 6; 0.5 +/- 0.6; p < 0.01). In HSPN, the number of m acrophages per glomerulus (n = 8; 1.9 +/- 1.0) was higher than that in IgA-N (n = 13; 0.9 +/- 0.9; p < 0.05). Based on these results, we con clude that XFb is often produced and distributed in intact form in the glomeruli both in IgA-N and HSPN, associated with a relatively low in traglomerular plasmin activity, and that intraglomerular coagulation m ay progress in accordance with macrophage infiltration, especially in HSPN.