A RANDOMIZED PROSPECTIVE TRIAL OF PROPHYLACTIC IMMUNOSUPPRESSION WITH ATG-FRESENIUS VERSUS OKT3 AFTER RENAL-TRANSPLANTATION

被引:80
作者
BOCK, HA
GALLATI, H
ZURCHER, RM
BACHOFEN, M
MIHATSCH, MJ
LANDMANN, J
THIEL, G
机构
[1] KANTONSSPITAL,DEPT INTERNAL MED,DIV NEPHROL & ORGAN TRANSPLANTAT,BASEL,SWITZERLAND
[2] KANTONSSPITAL,DEPT PATHOL,BASEL,SWITZERLAND
[3] KANTONSSPITAL,DEPT SURG,BASEL,SWITZERLAND
[4] F HOFFMANN LA ROCHE & CO LTD,BASEL,SWITZERLAND
关键词
D O I
10.1097/00007890-199503270-00006
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 carried out a randomized prospective trial to compare OKT3 (5 mg/d, 51 patients) with ATG-Fresenius (ATG-F, 4 mg/kg/d, 53 patients) for induction therapy after renal transplantation, concerning side effects, rejection, and infection incidence within a one year follow-up period. Concomitant immunosuppression included azathioprine/steroids from day 0 and cyclosporine A from day 4. OKT3 patients experienced significantly more and more-severe side effects, particularly pyrexia, headache, and pulmonary fluid overload. One-year graft survival was excellent in the ATG-F group (91%), but only 78% in the OKT3 group (P<0.05) due to a series of rejections that occurred beyond day 100; patient survival (96% and 92%) was similar in both groups. OKT3-treated patients experienced more biopsy-proven rejections (0.6+/-0.1/pt.) than ATG-F patients (0.3+/-0.1, P<0.05), and there was a similar, albeit not significant trend in clinical rejections (OKT3: 1.1+/-0.2/pt.; ATG-F: 0.8+/-0.1/pt.). Infections were more common in the OKT3 group (OKT3: 3.2+/-0.3, ATG-F: 2.0+/-0.2, P<0.05), although this was entirely attributable to ''minor'' infections. On days 1 through 6, CD3 counts were more profoundly depressed with OKT3 therapy. Beyond day 10, however, CD3 counts were lower in the ATG-F group, as were CD2 counts, CD4 counts, and the CD4/CD8 ratio, suggesting a more prolonged immunosuppressive effect of ATG-F. Sensitization occurred more frequently with OKT3 (31%) than with ATG-F (10%), but was usually irrelevant, except in two patients (one in each group), whose grafts were lost because of immunization against OKT3 and ATG-F, respectively. In conclusion, a 7-day induction therapy with OKT3 does not improve outcome or diminish immunological graft loss when compared with ATG-F, but is associated with more rejections, infections, and side effects. ATG-F appears to be preferable for induction immunosuppression after renal transplantation.
引用
收藏
页码:830 / 840
页数:11
相关论文
共 24 条
[1]  
CHATENOUD L, 1989, NEW ENGL J MED, V320, P1420
[2]   HUMAN INVIVO ANTIGENIC MODULATION INDUCED BY THE ANTI-T-CELL OKT3 MONOCLONAL-ANTIBODY [J].
CHATENOUD, L ;
BAUDRIHAYE, MF ;
KREIS, H ;
GOLDSTEIN, G ;
SCHINDLER, J ;
BACH, JF .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1982, 12 (11) :979-982
[3]   CORTICOSTEROID INHIBITION OF THE OKT3-INDUCED CYTOKINE-RELATED SYNDROME - DOSAGE AND KINETICS PREREQUISITES [J].
CHATENOUD, L ;
LEGENDRE, C ;
FERRAN, C ;
BACH, JF ;
KREIS, H .
TRANSPLANTATION, 1991, 51 (02) :334-338
[4]   A COMPARISON OF RABBIT ANTITHYMOCYTE-SERUM AND OKT3 AS PROPHYLAXIS AGAINST RENAL-ALLOGRAFT REJECTION [J].
COLE, EH ;
CATTRAN, DC ;
FAREWELL, VT ;
APRILE, M ;
BEAR, RA ;
PEI, YP ;
FENTON, SS ;
TOBER, JAL ;
CARDELLA, CJ .
TRANSPLANTATION, 1994, 57 (01) :60-67
[5]   USE OF MONOCLONAL-ANTIBODIES TO T-CELL SUBSETS FOR IMMUNOLOGICAL MONITORING AND TREATMENT IN RECIPIENTS OF RENAL-ALLOGRAFTS [J].
COSIMI, AB ;
COLVIN, RB ;
BURTON, RC ;
RUBIN, RH ;
GOLDSTEIN, G ;
KUNG, PC ;
HANSEN, WP ;
DELMONICO, FL ;
RUSSELL, PS .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (06) :308-314
[6]   ACTIVATION OF HUMAN T-CELLS INVIVO FOLLOWING TREATMENT OF TRANSPLANT RECIPIENTS WITH OKT3 [J].
ELLENHORN, JDI ;
WOODLE, ES ;
GHOBREAL, I ;
THISTLETHWAITE, JR ;
BLUESTONE, JA .
TRANSPLANTATION, 1990, 50 (04) :608-612
[7]   A PHASE-I TRIAL OF INTRAVENOUSLY-ADMINISTERED RECOMBINANT TUMOR NECROSIS FACTOR-ALPHA IN CANCER-PATIENTS [J].
FEINBERG, B ;
KURZROCK, R ;
TALPAZ, M ;
BLICK, M ;
SAKS, S ;
GUTTERMAN, JU .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (08) :1328-1334
[8]   SEQUENTIAL THERAPY - A PROSPECTIVE RANDOMIZED TRIAL OF MALG VERSUS OKT3 FOR PROPHYLACTIC IMMUNOSUPPRESSION IN CADAVER RENAL-ALLOGRAFT RECIPIENTS [J].
FREY, DJ ;
MATAS, AJ ;
GILLINGHAM, KJ ;
CANAFAX, D ;
PAYNE, WD ;
DUNN, DL ;
SUTHERLAND, DER ;
NAJARIAN, JS .
TRANSPLANTATION, 1992, 54 (01) :50-56
[9]   PHARMACOKINETIC STUDY OF ORTHOCLONE OKT3 SERUM LEVELS DURING TREATMENT OF ACUTE RENAL-ALLOGRAFT REJECTION [J].
GOLDSTEIN, G ;
NORMAN, DJ ;
HENELL, KR ;
SMITH, IL .
TRANSPLANTATION, 1988, 46 (04) :587-589
[10]   OKT3 MONOCLONAL-ANTIBODY PLASMA-LEVELS DURING THERAPY AND THE SUBSEQUENT DEVELOPMENT OF HOST ANTIBODIES TO OKT3 [J].
GOLDSTEIN, G ;
FUCCELLO, AJ ;
NORMAN, DJ ;
SHIELD, CF ;
COLVIN, RB ;
COSIMI, AB .
TRANSPLANTATION, 1986, 42 (05) :507-511