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Updated: Aug 23, 2026

Mouse Kidney Transplantation: Models of Allograft Rejection
Published on: October 11, 2014
Risk factors for capillary C4d deposition in kidney allografts: evaluation of a large study cohort
Matthias Lorenz1, Heinz Regele, Martin Schillinger
1Department of Internal Medicine III, University of Vienna, Vienna, Austria.
Insights
Administering immunosuppression before kidney transplant may reduce C4d deposition and graft dysfunction. Early initiation of calcineurin inhibitor or mycophenolate mofetil therapy before surgery is linked to better outcomes.
Area of Science:
- Nephrology
- Immunology
- Transplantation Medicine
Background:
- C4d deposition in kidney allografts is a marker for antibody-mediated rejection.
- The influence of pre- and post-transplant variables on C4d deposition requires further investigation.
Purpose of the Study:
- To investigate the impact of pre- and post-transplant variables, including immunosuppressive regimens, on C4d deposition in kidney transplant recipients.
Main Methods:
- Retrospective analysis of 388 kidney transplant recipients with diagnostic biopsies within 6 months post-transplant.
- Multivariate logistic regression used to analyze confounders affecting C4d-positive graft dysfunction.
Main Results:
- 17% of recipients showed C4d deposits, associated with lower 1-year allograft survival (73% vs. 88%).
- Pre-transplant initiation of calcineurin inhibitor or mycophenolate mofetil (MMF) reduced odds of C4d-positive dysfunction by 50%.
- Retransplantation and presensitization were independent risk factors for C4d deposition.
Conclusions:
- Early immunosuppression administration before kidney transplantation may reduce the risk of C4d-positive graft dysfunction.
- The timing of the first immunosuppressive dose, not specific drug choices, appears crucial for C4d staining results.
Background:
Capillary deposition of the complement split product C4d has turned out to be a valuable marker of antibody-mediated rejection. The impact of pre- and posttransplant variables including particular immunosuppressive regimens on the frequency of C4d deposition has not yet been systematically investigated in a large multivariate analysis.
Methods:
In this retrospective study, the authors evaluated the incidence of C4d deposition in 388 kidney transplant recipients subjected to diagnostic biopsy within the first 6 months and analyzed the influence of potential confounders on the rate of C4d-positive graft dysfunction by applying multivariate logistic regression.
Results:
Sixty-six recipients (17%) developed linear C4d deposits in at least a quarter of peritubular capillaries, a finding associated with inferior 1-year allograft survival (73% vs. 88% in C4d-negative patients, P=0.0003). A 50% reduction in the odds of C4d-positive graft dysfunction was found if calcineurin inhibitor or mycophenolate mofetil (MMF) therapy was started 2 to 4 hr before transplantation when compared with initiation after surgery (adjusted odds ratio [OR], 0.5; P=0.03). No differences with respect to C4d staining results were found for the use of tacrolimus, MMF, or sirolimus, or for cyclosporine C2 monitoring. Retransplantation (OR, 3.6; P<0.001) and presensitization (OR, 3.1; P=0.002) turned out to be strong independent risk factors for C4d deposition.
Conclusions:
The authors' results suggest a reduced risk of C4d-positive graft dysfunction for patients receiving immunosuppression before transplantation. Apart from first dose timing, no influence of particular immunosuppressive strategies on C4d staining results was found.
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