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Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Immunofluorescent microscopic findings in glomerulonephritis
S Tabassum1, K M Rahman, K Z Mamun
1Department of Microbiology, Institute of Postgraduate Medicine & Research, Dhaka.
Insights
Direct immunofluorescence (DIF) aids glomerulonephritis (GN) diagnosis by detecting immune deposits. DIF confirmed immune complex deposition in various GN types, proving valuable when histopathology is inconclusive.
Area of Science:
- Nephrology
- Immunopathology
- Renal Pathology
Background:
- Glomerulonephritis (GN) diagnosis relies on renal biopsy interpretation.
- Histopathology and direct immunofluorescence (DIF) are key diagnostic tools.
- Understanding immune complex deposition patterns is crucial for GN classification.
Purpose of the Study:
- To evaluate the diagnostic utility of histopathology and DIF in suspected glomerulonephritis.
- To correlate immune complex deposition patterns with specific GN subtypes.
- To assess DIF's role in cases with inconclusive histopathological findings.
Main Methods:
- Sixty renal biopsy specimens from clinically suspected GN cases were analyzed.
- Histopathological examination was performed on all specimens.
- Direct immunofluorescence (DIF) microscopy was used to detect immune deposits.
Main Results:
- Histopathological diagnosis was achieved in 73.3% of cases.
- DIF detected immune complex deposition in 46.7% of cases.
- Immune deposits were present in membranous GN, SLE, RPGN, diffuse proliferative GN, mesangioproliferative GN, and focal glomerulosclerosis; absent in minimal change, chronic GN, and diabetic nephropathy.
- DIF identified immune deposits in 3 cases (5%) where histopathology was inconclusive.
Conclusions:
- DIF is a valuable adjunct to histopathology in diagnosing glomerulonephritis.
- The presence and pattern of immune deposits identified by DIF aid in classifying GN.
- DIF can provide diagnostic clues in cases where histopathology alone is insufficient.
Abstract:
Histopathology and direct immunofluorescence (DIF) microscopy were performed on renal biopsy specimens of 60 clinically suspected cases of glomerulonephritis (GN). Histopathological diagnosis was obtained in 44 (73.3%) cases and immune complex deposition were detected by DIF in 28 (46.7%) cases. Immune complex deposition were observed in all cases of membranous GN, systemic lupus erythematosus (SLE), and rapidly progressive GN (RPGN), most of the cases of diffuse proliferative GN (2 out of 3) mesangioproliferative GN (12 out of 15) and focal glomeruloscleros is (3 out of 5 cases). No immune deposits were observed in minimal change GN, chronic GN, and diabetic nephropathy. Histopathological diagnosis was not obtained in 16 (26.7%) cases, 3 (5%) of which showed immune complex deposition by DIF. Anti-GBM nephritis was demonstrated in one (3.6%) case, the rest were immune complex nephritis.
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