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The potential role of antimetabolite in preventing allosensitization before kidney retransplantation
Madeleine Thommen1, Lukas Weidmann1, Dusan Harmacek1
1Department of Nephrology, University Hospital of Zurich, Zurich, Switzerland.
Background And Aims:
Retransplantation is becoming more common. Allosensitization represents an increasing issue, as it prolongs the time on the waiting list and worsens the outcome of a second transplant. The optimal maintenance immunosuppression (IS) after graft failure remains unclear.
Methods:
This is a retrospective single-center study including kidney retransplant recipients (KRTRs) who underwent a retransplantation in the University Hospital of Zurich between 2012 and 2023. We analyzed which factors and especially which kind of maintenance IS after graft failure could affect allosensitization.
Results:
In our cohort, 191/1,040 (16%) were retransplantations. Of the included KRTRs, 27/129 (20%) were living donations (LDs). The median waiting time for deceased donations (DDs) was 4 years. The burden of IS decreased from graft failure to retransplantation (triple IS 54 vs. 12%, p < 0.05), while the allosensitization increased [number of HLA-antibodies (Ab) MFI > 1,000/patient 5.8 vs. 12.45, p > 0.001]. In the univariate analysis transplant, nephrectomy was associated with a higher calculated panel reactive Ab (cPRA): 90 vs. 29 (p < 0.0001). At retransplantation, intake of calcineurin inhibitor (CNI) was associated with lower cPRA (27% vs. 78% no CNI, p < 0.001), as was intake of antimetabolite [23% for azathioprine, 20% for mycophenolic acid (MPA), and 88% for no antimetabolite, p < 0.001] and of prednisone (PDN) (24% vs. 66% no PDN, p = 0.02). First retransplantation was also associated with a lower cPRA when compared to a second or a third retransplantation (41% vs. 78% vs. 88%, p = 0.02). In the multivariable analysis, only the intake of antimetabolite remained associated with cPRA <85% at retransplantation. Surprisingly, we could find a weak correlation between cPRA and waiting time to retransplantation (r = 0.25, R 2 = 0.06, p = 0.01).
Conclusion:
The intake of antimetabolite at retransplantation showed a protective effect against allosensitization. Waiting time to retransplantation had only a weak correlation with allosensitization over the whole cPRA spectrum in this Swiss cohort study.
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