SYMPTOMATIC CYTOMEGALOVIRUS-INFECTION IN RENAL-TRANSPLANT RECIPIENTS GIVEN EITHER MINNESOTA ANTILYMPHOBLAST GLOBULIN (MALG) OR OKT3 FOR REJECTION PROPHYLAXIS

被引:25
作者
BAILEY, TC
POWDERLY, WG
STORCH, GA
MILLER, SB
DUNKEL, JD
WOODWARD, RS
SPITZNAGEL, E
HANTO, DW
DUNAGAN, WC
机构
[1] WASHINGTON UNIV,SCH MED,DEPT INTERNAL MED,DIV INFECT DIS,ST LOUIS,MO 63110
[2] WASHINGTON UNIV,SCH MED,DEPT INTERNAL MED,DIV RENAL,ST LOUIS,MO 63110
[3] WASHINGTON UNIV,SCH MED,DEPT SURG,HLTH ADM PROGRAM,ST LOUIS,MO 63110
[4] WASHINGTON UNIV,SCH MED,DEPT SURG,DIV BIOSTAT,ST LOUIS,MO 63110
[5] WASHINGTON UNIV,SCH MED,DEPT SURG,TRANSPLANTAT SECT,ST LOUIS,MO 63110
关键词
CYTOMEGALIC INCLUSION DISEASE; RISK FACTOR ANALYSIS; ANTILYMPHOBLAST GLOBULIN; OKT3; KIDNEY TRANSPLANTATION;
D O I
10.1016/S0272-6386(12)81093-6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
To compare the impact of using Minnesota antilymphoblast globulin (MALG) versus the monoclonal antibody, OKT3, on the development of symptomatic cytomegalovirus (CMV) infection, we reviewed a cohort of 130 cadaveric renal transplant recipients enrolled in a prospective comparison of MALG versus OKT3 for rejection prophylaxis. Among the 112 patients at risk for CMV, prophylactic MALG was associated with an increased risk of symptomatic infection (relative hazard [rhj = 3.31; 95% confidence interval CI], 1.50 to 7.30; P = 0.003). Transplantation of kidneys from CMV-seropositive donors into CMV-seronegative recipients (rh = 5.22; 95% CI, 2.34 to 11.63; P = 0.00004), first transplantation (rh = 4.76; 95% CI, 1.06 to 21.3; P = 0.039), and acute rejection therapy (rh = 2.03; 95% CI, 0.98 to 4.21; P = 0.055) were also associated with an increased risk. Prophylactic MALG followed by treatment with any agent for acute rejection was strongly correlated with symptomatic CMV infection (rh = 4.46; 95% CI, 3.71 to 5.21; P = 0.00006). Symptomatic CMV infection was not only more frequent, but more severe in recipients of prophylactic MALG, and more MALG recipients were treated with ganciclovir. There was no difference in rejection rate for the two rejection prophylaxis regimens (P = 0.625). Prophylactic OKT3 results in less risk of symptomatic CMV infection than prophylactic MALG in cadaveric renal transplant recipients who are seropositive for CMV or whose donors are seropositive for CMV. CMV prophylaxis studies or immunosuppression protocols with symptomatic CMV infection as an end point should be stratified according to the type of antilymphocyte therapy used for rejection prophylaxis, as well as donor and recipient CMV serologic status. © 1993, National Kidney Foundation. All rights reserved. All rights reserved.
引用
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页码:196 / 201
页数:6
相关论文
共 27 条
[1]
A RANDOMIZED, PLACEBO-CONTROLLED TRIAL OF ORAL ACYCLOVIR FOR THE PREVENTION OF CYTOMEGALO-VIRUS DISEASE IN RECIPIENTS OF RENAL-ALLOGRAFTS [J].
BALFOUR, HH ;
CHACE, BA ;
STAPLETON, JT ;
SIMMONS, RL ;
FRYD, DS .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (21) :1381-1387
[2]
THE PREVENTION OF CYTOMEGALOVIRUS DISEASE IN RENAL-TRANSPLANTATION [J].
DAVIS, CL .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1990, 16 (03) :175-188
[3]
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
[4]
FREY DJ, 1991, TRANSPLANT P, V23, P1048
[5]
CYTOMEGALO-VIRUS AS A RISK FACTOR IN RENAL-TRANSPLANTATION [J].
FRYD, DS ;
PETERSON, PK ;
FERGUSON, RM ;
SIMMONS, RL ;
BALFOUR, HH ;
NAJARIAN, JS .
TRANSPLANTATION, 1980, 30 (06) :436-439
[6]
GOLDSTEIN G, 1985, NEW ENGL J MED, V313, P337
[7]
A MULTIVARIATE-ANALYSIS OF THE RISK OF CYTOMEGALO-VIRUS INFECTION IN HEART-TRANSPLANT RECIPIENTS [J].
GORENSEK, MJ ;
STEWART, RW ;
KEYS, TF ;
MCHENRY, MC ;
GOORMASTIC, M .
JOURNAL OF INFECTIOUS DISEASES, 1988, 157 (03) :515-522
[8]
HEGEWALD MG, 1989, J HEART TRANSPLANT, V8, P303
[9]
HO M, 1990, REV INFECT DIS, V12, pS701
[10]
HO M, 1991, CYTOMEGALOVIRUS BIOL, P259