THE LONG-TERM EFFECTS OF PROPHYLACTIC OKT3 MONOCLONAL-ANTIBODY IN CADAVER KIDNEY-TRANSPLANTATION - A SINGLE-CENTER, PROSPECTIVE, RANDOMIZED STUDY

被引:64
作者
ABRAMOWICZ, D [1 ]
GOLDMAN, M [1 ]
DEPAUW, L [1 ]
VANHERWEGHEM, JL [1 ]
KINNAERT, P [1 ]
VEREERSTRAETEN, P [1 ]
机构
[1] CLIN UNIV BRUXELLES, HOP ERASME, DEPT IMMUNOL, BRUSSELS, BELGIUM
关键词
D O I
10.1097/00007890-199209000-00009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We conducted a randomized, prospective study to determine the long-term effects of prophylactic OKT3 in cadaveric renal transplantation. In the first group of patients (n=56) OKT3 (5 mg/day) was administered for the first 14 postoperative days in association with azathioprine (AZA) and low-dose steroids, cyclosporine (CsA) being introduced on day 11. The other group of patients (n=52) received CsA from the first POD, together with AZA and steroids. Both protocols were identical from POD 14 on. The total number of infections was higher in OKT3 patients (124/1455 patient-months [P-M] vs. 68/1320 in CsA patients, P<0.001) without impact on patient survival (94.5% in OKT3 vs. 93% in CsA patients). OKT3 patients experienced a lower number of rejection episodes (61 per 1455 P-M of risk exposure vs. 81/1320 in CsA patients, P<0.05). In addition, the frequency of corticoresistant rejection episodes was lower in OKT3 patients (9 out of 61 vs. 24 out of 81 in CsA patients, P<0.05). This resulted in a trend toward improved overall graft survival (83% vs. 75%, P=0.12) and in a significant increase in immunological graft survival (92% vs. 79%, P=0.02) in OKT3 patients at 3 years. Taken together, these data suggest that prophylactic OKT3 therapy might have long-term beneficial effects in cadaveric renal transplantation.
引用
收藏
页码:433 / 437
页数:5
相关论文
共 39 条
[1]   RELEASE OF TUMOR NECROSIS FACTOR, INTERLEUKIN-2, AND GAMMA-INTERFERON IN SERUM AFTER INJECTION OF OKT3 MONOCLONAL-ANTIBODY IN KIDNEY-TRANSPLANT RECIPIENTS [J].
ABRAMOWICZ, D ;
SCHANDENE, L ;
GOLDMAN, M ;
CRUSIAUX, A ;
VEREERSTRAETEN, P ;
DEPAUW, L ;
WYBRAN, J ;
KINNAERT, P ;
DUPONT, E ;
TOUSSAINT, C .
TRANSPLANTATION, 1989, 47 (04) :606-608
[2]  
ABRAMOWICZ D, 1991, NEW ENGL J MED, V324, P1438
[3]  
ACUTO O, 1985, NEW ENGL J MED, V312, P1100
[4]  
ALEGRE ML, 1991, J IMMUNOL, V146, P1184
[5]   INDUCTION OF SPECIFIC NONRESPONSIVENESS IN UNPRIMED HUMAN T-CELLS BY ANTI-CD3 ANTIBODY AND ALLOANTIGEN [J].
ANASETTI, C ;
TAN, P ;
HANSEN, JA ;
MARTIN, PJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1691-1700
[6]   IMPROVED RESULTS USING OKT3 AS INDUCTION IMMUNOSUPPRESSION IN RENAL-ALLOGRAFT RECIPIENTS WITH DELAYED GRAFT FUNCTION [J].
BENVENISTY, AI ;
COHEN, D ;
STEGALL, MD ;
HARDY, MA .
TRANSPLANTATION, 1990, 49 (02) :321-327
[7]   DOES OKT3 MONOCLONAL-ANTIBODY REACT WITH AN ANTIGEN-RECOGNITION STRUCTURE ON HUMAN T-CELLS [J].
CHANG, TW ;
KUNG, PC ;
GINGRAS, SP ;
GOLDSTEIN, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (03) :1805-1808
[8]  
CHATENOUD L, 1989, NEW ENGL J MED, V320, P1420
[9]   ONE-MONTH PROPHYLACTIC USE OF OKT3 IN CADAVER KIDNEY-TRANSPLANT RECIPIENTS [J].
DEBURE, A ;
CHKOFF, N ;
CHATENOUD, L ;
LACOMBE, M ;
CAMPOS, H ;
NOEL, LH ;
GOLDSTEIN, G ;
BACH, JF ;
KREIS, H .
TRANSPLANTATION, 1988, 45 (03) :546-553
[10]   EVOLUTION OF RENAL-FUNCTION DURING TREATMENT OF KIDNEY GRAFT-REJECTION WITH OKT3 MONOCLONAL-ANTIBODY [J].
GOLDMAN, M ;
VANLAETHEM, JL ;
ABRAMOWICZ, D ;
DEPAUW, L ;
KINNAERT, P ;
VEREERSTRAETEN, P .
TRANSPLANTATION, 1990, 50 (01) :158-159