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Epidemiology and Pathophysiology of Glomerular C4d Staining in Native Kidney Biopsies
Cinthia B Drachenberg1, John C Papadimitriou1, Preeti Chandra2
1Department of Pathology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Insights
C4d staining in native kidney biopsies shows distinct patterns across various glomerular diseases. This diagnostic tool is particularly useful for lupus nephritis and membranous GN, aiding in screening and diagnosis when only paraffin-embedded tissue is available.
Area of Science:
- Nephrology
- Immunopathology
- Diagnostic Pathology
Background:
- C4d staining is routinely used in renal transplantation.
- Its application in native kidney biopsies for glomerulonephritis (GN) is increasing.
- A systematic description of C4d staining patterns in native kidneys is lacking.
Purpose of the Study:
- To describe C4d staining patterns in native kidney biopsies.
- To evaluate the diagnostic utility of C4d in various glomerular diseases.
- To correlate C4d staining with specific histopathological findings.
Main Methods:
- Retrospective analysis of 519 native kidney biopsies.
- Evaluation of C4d staining in formalin-fixed, paraffin-embedded tissue sections.
- Comparison of staining patterns across different glomerular diseases and normal biopsies.
Main Results:
- Strong C4d staining was observed in immune-complex GN, including lupus nephritis and membranous GN.
- Variable or negative staining was noted in IgA nephropathy.
- C4d highlighted specific lesions in thrombotic microangiopathy, FSGS, crescentic GN, and diabetic glomerulopathy.
- Weak or negative staining was typical in minimal change disease, thin basement membrane disease, and normal biopsies.
Conclusions:
- C4d staining demonstrates characteristic patterns in various native kidney diseases.
- It shows potential as a screening and diagnostic tool, especially for lupus nephritis and membranous GN.
- Understanding C4d staining patterns enhances its diagnostic value in native kidney biopsies.
Introduction:
Routine C4d staining in renal transplantation has stimulated its use in kidney biopsies with glomerulonephritis (GN). Methodical description on staining patterns in the native kidney is not available.
Methods:
We retrospectively evaluated C4d staining in formalin-fixed paraffin-embedded sections from 519 native kidney biopsies (bx) with and without glomerular disease.
Results:
Strong C4d staining was consistently present in immune-complex GN, including lupus nephritis (LN) (n = 68), membranous GN (n = 24), membranoproliferative glomerulonephritis (MPGN) pattern (n = 22), fibrillary GN (n = 3), and proliferative GN with monoclonal IgG (n = 3). C4d stained all cases of postinfectious GN (n = 7) amyloidosis (n = 20) and C1q GN (n = 3). In contrast, IgA nephropathy (IgAN) (n = 34), was negative in 62% of bx, with the rest staining variably. The E1 Oxford classification score correlated with capillary wall C4d staining (P = 0.05). C4d marked the glomerular and arteriolar lesions in thrombotic microangiopathy (TMA; n = 16), the glomerular sclerotic segments in focal segmental glomerulosclerosis (FSGS; n = 77), and marked areas of necrosis in crescentic GN (n = 21). In diabetic glomerulopathy (n = 70), C4d marked advanced insudative lesions but was negative otherwise. C4d weakly stained the mesangium, or was negative in normal biopsies (n = 13), minimal change disease (MCD; n = 21), thin basement membrane disease (n = 20), Alport (n = 3), IgM nephropathy (n = 2), C3 glomerulopathy (n = 5), acute interstitial nephritis (n = 12), acute tubular necrosis (n = 22), ischemic glomerulopathy/nephrosclerosis (n = 23), and other miscellaneous processes (n = 14). Staining in tubular basement membranes and peritubular capillaries was most common in lupus.
Conclusion:
Based on reliable staining in lupus and membranous GN, C4d staining is potentially useful as a screening and diagnostic tool, if only paraffin-embedded tissue is available. Knowledge of C4d staining patterns in normal and pathological tissues enhances its diagnostic value.
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