OKT3 Treatment for Steroid-Resistant Acute Rejection in Kidney Transplantation

Orthoclone (OKT3, Ortho Biotech Inc, USA) monoclonal antilymphocyte antibody is a powerful T-cell–specific immunosuppressive agent. OKT3 has been used for induction therapy in kidney and liver transplantation, as well as to treat acute or steroid-resistant acute rejection episodes (ARE). This study...

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Veröffentlicht in:Transplantation proceedings 2005-09, Vol.37 (7), p.3016-3018
Hauptverfasser: Sevmis, S., Emiroglu, R., Karakayali, F., Yagmurdur, M.C., Dalgic, A., Moray, G., Haberal, M.
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Sprache:eng
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Zusammenfassung:Orthoclone (OKT3, Ortho Biotech Inc, USA) monoclonal antilymphocyte antibody is a powerful T-cell–specific immunosuppressive agent. OKT3 has been used for induction therapy in kidney and liver transplantation, as well as to treat acute or steroid-resistant acute rejection episodes (ARE). This study was a retrospective analysis of 43 renal transplant recipients who developed steroid-resistant ARE and were treated with OKT3 between September 1994 and June 2004. The recipients were 36 men and 7 women of mean age 32.7 ± 11.6 years (range, 19 to 48 years). The mean time from transplantation to OKT3 treatment was 7.2 ± 6.7 months. Thirty-four episodes (79.1%) responded to OKT3 therapy with improved graft function, but the remaining 9 (20.9%) grafts did not respond. Among the 34 OKT3 responders, the mean serum creatinine decreased from 3.96 ± 2.5 mg/dL to 2.45 ± 1.77 mg/dL after treatment. Eleven (25.6%) of the 43 patients experienced minor side effects: fever, dyspnea, tachycardia, bradycardia. One patient (2.3%) developed acute pulmonary edema; one (2.3%), cytomegalovirus infection; and eight (18.6%), bacterial infections. The 1-, 3-, and 5-year graft survival rates for the 34 patients who responded to OKT3 therapy were 96%, 93%, and 85%, respectively. All patients are currently alive. The results indicate that OKT3 is a safe, effective treatment choice for steroid-resistant ARE in kidney transplantation.
ISSN:0041-1345
1873-2623
DOI:10.1016/j.transproceed.2005.07.052