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OKT3 prophylaxis in cadaveric kidney transplant recipients with delayed graft function
D J Cohen1, A I Benvenisty, J Cianci
1Department of Medicine, Columbia University College of Physicians and Surgeons, Presbyterian Hospital, New York, NY 10032.
Summary
OKT3 monoclonal antibody prophylaxis improved 1-year survival for kidney transplant recipients with acute tubular necrosis (ATN), outperforming early cyclosporine treatment. This approach also shortened ATN duration and delayed rejection episodes.
Area of Science:
- Nephrology
- Immunology
- Transplantation
Background:
- Decreased 1-year renal allograft survival is common in patients with postoperative acute tubular necrosis (ATN).
- Cyclosporine use can prolong ATN, while withholding it risks early rejection.
- Polyclonal antilymphocyte antibodies have been used to prevent rejection and avoid cyclosporine nephrotoxicity.
Purpose of the Study:
- To evaluate the efficacy of OKT3 monoclonal antibody prophylaxis in cadaveric renal allograft recipients experiencing ATN.
- To compare outcomes of OKT3 prophylaxis with early cyclosporine treatment in ATN patients.
- To compare outcomes with recipients experiencing immediate graft function.
Main Methods:
- Retrospective comparison of cadaveric renal allograft recipients with ATN.
- Group 1: Received OKT3 monoclonal antibody prophylaxis (n=26) starting January 1987.
- Group 2: Received cyclosporine treatment during ATN (n=40) in 1985-1986.
Main Results:
- 1-year graft survival was significantly higher with OKT3 prophylaxis (83%) versus early cyclosporine (55%).
- No significant difference in 1-year graft survival between OKT3-treated ATN patients and those with immediate graft function (74%).
- OKT3 prophylaxis shortened ATN duration (9.3 days vs 14.9 days) and prolonged median time to first rejection (23.5 days vs 11.0 days).
Conclusions:
- OKT3 monoclonal antibody prophylaxis offers superior 1-year graft survival in renal transplant recipients with ATN compared to early cyclosporine.
- OKT3 prophylaxis effectively manages ATN, reduces rejection risk, and improves graft outcomes.
- Patient survival was not affected by ATN or the immunosuppressive protocol used.