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Published on: August 19, 2020
Glomerular C4d deposition in proliferative glomerular diseases
Sarojini Raman1, Pallavi Mishra1, Ansuman Panigrahi2
1Department of Pathology, Kalinga Institute of Medical Sciences, Bhubaneswar, Odisha, India.
Insights
C4d deposition is common in proliferative glomerular diseases, particularly associated with IgG and IgM staining. This finding aids in understanding complement pathways and disease pathogenesis.
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- Proliferative glomerular diseases involve complex complement pathways.
- Immunohistochemical evaluation of C4d aids in understanding renal pathology.
- C4d deposition is a marker of complement activation in kidney diseases.
Purpose of the Study:
- To evaluate C4d expression in native renal biopsies of proliferative glomerular diseases.
- To investigate the role of complement pathways in these diseases.
- To correlate C4d with histological, clinical, and immunological markers.
Main Methods:
- Cross-sectional study of 107 native renal biopsies diagnosed with proliferative glomerular diseases.
- Immunohistochemistry using polyclonal anti-human C4d antibody.
- Classification of patients based on glomerular C4d deposition (positive/negative).
Main Results:
- Overall C4d positivity was 80.4% in proliferative glomerular diseases.
- C4d positivity ranged from 60.0% in C3 glomerulonephritis to 92.9% in membranoproliferative glomerulonephritis.
- Glomerular IgG and IgM staining were significantly associated with C4d positivity (aOR: 5.86 and 3.90, respectively).
Conclusions:
- C4d staining, alongside immunoglobulin markers (IgG, IgM), helps delineate complement activation pathways.
- This approach aids in understanding the pathogenesis of glomerular diseases.
- C4d evaluation is a valuable tool in diagnosing and characterizing proliferative glomerular diseases.
Introduction:
The aim of this study was to evaluate the immunohistochemical expression of C4d in native renal biopsies of proliferative glomerular diseases, complement pathways in these diseases, and assess the relationship of C4d with histological and clinicopathological parameters, other complement proteins, and immunoglobulin markers.
Methods:
This cross-sectional study was conducted during the year 2018-19 involving 107 native renal biopsies with histologically diagnosed cases of proliferative glomerular diseases. C4d immunohistochemical evaluation of renal tissue sections was performed using polyclonal antihuman C4d as the primary antibody. Patients were classified as positive and negative groups based on their glomerular C4d deposition.
Results:
The overall prevalence of C4d positivity was 80.4% in proliferative glomerular diseases ranging between 60.0% in C3 glomerulonephritis to 92.9% in membranoproliferative glomerulonephritis. Mixed capillary and mesangial deposition were noted in all cases of proliferative glomerulonephritis. Classical pathway was dominantly involved in all glomerular diseases except C3 glomerulonephritis and IgA nephropathy. Multivariate logistic regression analysis revealed that glomerular IgG staining (aOR: 5.86, 95% CI: 1.26-27.14) and IgM staining (aOR: 3.90, 95%CI: 1.07-14.18) were significantly associated with C4d positivity.
Conclusion:
C4d staining along with immunoglobulin markers such as IgG and IgM and complement proteins can be useful in delineating different complement activation pathways in glomerular diseases and understanding the disease pathogenesis.
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