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Updated: Jan 31, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Insights
Complement activation is key in kidney diseases. This review summarizes glomerular C4d deposition data, aiding research into complement
Area of Science:
- Nephrology
- Immunology
- Pathology
Background:
- Complement activation is implicated in numerous glomerular diseases.
- Specific complement pathway involvement is not fully elucidated for all glomerular pathologies.
- C4d deposition indicates activation of the classical or lectin complement pathways.
Purpose of the Study:
- To review and synthesize existing data on glomerular C4d deposition in native kidney biopsies.
- To highlight C4d's role across various glomerular diseases.
- To identify knowledge gaps and guide future research on complement's role in glomerular diseases.
Main Methods:
- Systematic review of literature concerning glomerular C4d deposition in native kidney biopsies.
- Analysis of data across different glomerular pathologies.
- Comparison of C4d data availability between distinct glomerular diseases.
Main Results:
- Glomerular C4d deposition is a marker for classical and lectin pathway activation in kidney diseases.
- Data on C4d deposition is more abundant for certain conditions like Immunoglobulin A (IgA) nephropathy.
- Scant data exists for C4d deposition in other diseases, such as focal segmental glomerulosclerosis.
Conclusions:
- Glomerular C4d deposition is a valuable indicator in understanding complement activation pathways in kidney disease.
- Further research is needed to fully understand the role of complement and C4d in less-studied glomerular pathologies.
- This review provides a foundation for future investigations into complement-driven kidney diseases.
Abstract:
Complement activation occurs in many glomerular diseases, the exact pathway(s) of activation has been studied in detail in some diseases but not in all. C4d is generated by the activation of classical and lectin pathways, and its presence can point to the activation of either of these pathways. This review aims to summarize the available data with regard to the deposition of glomerular C4d in native kidney biopsies in different glomerular pathologies that may be useful for future research into the role of complement activation in glomerular diseases. While there is more information on C4d in certain diseases (e.g., Immunoglobulin A (IgA) nephropathy), there is scant data in other diseases (such as focal segmental glomerulosclerosis).
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