Combination of Peritubular C4d and Transplant Glomerulopathy Predicts Late Renal Allograft Failure

Niamh E. Kieran(University of Washington), Xiaotong Wang(University of Washington), James D. Perkins(University of Washington), Connie L. Davis(University of Washington), Elizabeth Kendrick(University of Washington), Ramaswamy Bakthavatsalam(University of Washington), Nancy M. Dunbar(Bloodworks Northwest), Paul Warner(Bloodworks Northwest), Karen Nelson(Bloodworks Northwest), Kelly D. Smith(University of Washington), Roberto F. Nicosia(University of Washington), Charles E. Alpers(University of Washington), Nicolae Leca(University of Washington), Jolanta Kowalewska(University of Washington)
Journal of the American Society of Nephrology
September 4, 2009
Cited by 74Open Access
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Abstract

The histologic associations and clinical implications of peritubular capillary C4d staining from long-term renal allografts are unknown. We identified 99 renal transplant patients who underwent an allograft biopsy for renal dysfunction at least 10 yr after transplantation, 25 of whom were C4d-positive and 74 of whom were C4d-negative. The average time of the index biopsy from transplantation was 14 yr in both groups. Compared with C4d-negative patients, C4d-positive patients were younger at transplantation (29 +/- 13 versus 38 +/- 12 yr; P < 0.05) and were more likely to have received an allograft from a living donor (65 versus 35%; P < 0.001). C4d-positive patients had more inflammation, were more likely to have transplant glomerulopathy, and had worse graft outcome. The combined presence of C4d positivity, transplant glomerulopathy, and serum creatinine of >2.3 mg/dl at biopsy were very strong predictors of rapid graft loss. C4d alone did not independently predict graft loss. Retrospective staining of historical samples from C4d-positive patients demonstrated C4d deposition in the majority of cases. In summary, these data show that in long-term renal allografts, peritubular capillary staining for C4d occurs in approximately 25% of biopsies, can persist for many years after transplantation, and strongly predicts graft loss when combined with transplant glomerulopathy.


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