Pharmacokinetics of hyperimmune anti-human immunodeficiency virus immunoglobulin in persons with AIDS

被引:13
作者
Fletcher, CV
Goodroad, BK
Cummins, LM
Henry, K
Balfour, HH
Rhame, FS
机构
[1] UNIV MINNESOTA,ACAD HLTH CTR,DEPT PEDIAT,MINNEAPOLIS,MN 55455
[2] UNIV MINNESOTA,ACAD HLTH CTR,DEPT LAB MED & PATHOL,MINNEAPOLIS,MN 55455
[3] UNIV MINNESOTA,ACAD HLTH CTR,DEPT INFECT DIS,MINNEAPOLIS,MN 55455
[4] ST PAUL RAMSEY MED CTR,HUMAN IMMUNODEFICIENCY VIRUS & AIDS PROGRAMS,ST PAUL,MN 55101
[5] N AMER BIOL INC,BOCA RATON,FL
关键词
D O I
10.1128/AAC.41.7.1571
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hyperimmune anti-human immunodeficiency virus immunoglobulin (HIVIG) is an intravenous immunoglobulin prepared from HIV-infected asymptomatic donors with a CD4 cell count greater than 400 cells/mu l and a high titer of antibody to HIV-1 p24 protein. Twelve persons with AIDS received four doses of HMG (two at 50 mg/kg of body weight and then two at 200 mg/kg) every 28 days, Pharmacokinetics were evaluated by measurement of anti-p24 antibody. HIVIG was well tolerated, and all Participants completed the study. Three subjects who were not receiving Pneumocystis carinii pneumonia (PCP) prophylaxis developed PCP, The mean value for HMG clearance was 3.02 ml/kg/day at 50 mg/kg and 3.65 ml/kg/day at 200 mg/kg (P = 0.027); the mean trough antibody titers (reciprocal units) were 1,442 and 4,428, respectively. This study indicates that high titers of anti-p24 antibody can be maintained with a monthly administration Schedule of HMG and that short-term safety is acceptable. Comparisons to evaluate the therapeutic potential of HIVIG are justified.
引用
收藏
页码:1571 / 1574
页数:4
相关论文
共 18 条
[1]  
ALLAIN JP, 1986, LANCET, V2, P1233
[2]   LONG-TERM EVALUATION OF HIV ANTIGEN AND ANTIBODIES TO P24 AND GP41 IN PATIENTS WITH HEMOPHILIA - POTENTIAL CLINICAL IMPORTANCE [J].
ALLAIN, JP ;
LAURIAN, Y ;
PAUL, DA ;
VERROUST, F ;
LEUTHER, M ;
GAZENGEL, C ;
SENN, D ;
LARRIEU, MJ ;
BOSSER, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (18) :1114-1121
[3]  
BUCKLEY RH, 1991, NEW ENGL J MED, V325, P110, DOI 10.1056/NEJM199107113250207
[4]  
CUMMINS LM, 1991, BLOOD, V77, P1111
[5]   SIMULATION OF LINEAR COMPARTMENT MODELS WITH APPLICATION TO NUCLEAR-MEDICINE KINETIC MODELING [J].
DARGENIO, DZ ;
SCHUMITZKY, A ;
WOLF, W .
COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE, 1988, 27 (01) :47-54
[6]  
JACKSON GG, 1988, LANCET, V2, P647
[7]   EFFECTS OF PASSIVE-IMMUNIZATION IN PATIENTS WITH THE ACQUIRED IMMUNODEFICIENCY SYNDROME-RELATED COMPLEX AND ACQUIRED IMMUNODEFICIENCY SYNDROME [J].
KARPAS, A ;
HILL, F ;
YOULE, M ;
CULLEN, V ;
GRAY, J ;
BYRON, N ;
HAYHOE, F ;
TENANTFLOWERS, M ;
HOWARD, L ;
GILGEN, D ;
OATES, JK ;
HAWKINS, D ;
GAZZARD, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9234-9237
[8]   Safety and pharmacokinetics of hyperimmune anti-human immunodeficiency virus (HIV) immunoglobulin administered to HIV-infected pregnant women and their newborns [J].
Lambert, JS ;
Mofenson, LM ;
Fletcher, CV ;
Moye, J ;
Stiehm, ER ;
Meyer, WA ;
Nemo, GJ ;
Mathieson, BJ ;
Hirsch, G ;
Sapan, CV ;
Cummins, LM ;
Jimenez, E ;
ONeill, E ;
Kovacs, A ;
Stek, A .
JOURNAL OF INFECTIOUS DISEASES, 1997, 175 (02) :283-291
[9]  
LEVER AML, 1987, CLIN EXP IMMUNOL, V67, P441
[10]  
*NAT I CHILD HLTH, 1991, NEW ENGL J MED, V325, P73