EVALUATION OF THE PROTECTIVE EFFICACY OF RESHAPED HUMAN MONOCLONAL-ANTIBODY RSHZ19 AGAINST RESPIRATORY SYNCYTIAL VIRUS IN COTTON RATS

被引:35
作者
WYDE, PR
MOORE, DK
HEPBURN, T
SILVERMAN, CL
PORTER, TG
GROSS, M
TAYLOR, G
DEMUTH, SG
DILLON, SB
机构
[1] BAYLOR COLL MED,DEPT MICROBIOL & IMMUNOL,HOUSTON,TX 77030
[2] SMITHKLINE BEECHAM PHARMACEUT INC,KING OF PRUSSIA,PA 19406
[3] INST ANIM HLTH,COMPTON,ENGLAND
关键词
D O I
10.1203/00006450-199510000-00012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Reshaped human MAb RSHZ19, which is specific for the surface fusion protein of respiratory syncytial virus (RSV) is in clinical development for the prevention and treatment of RSV-induced disease in human infants. The current studies profile lung virus clearance and evaluate lung histopathology in MAb-treated, RSV-infected cotton rats, a well characterized model of RSV infection. The highest dose of this MAb (10 mg/kg) administered parenterally 24 h before infection decreased subgroup A or B RSV lung titers to below detectable levels (greater than or equal to 2.3 log(10) reduction), and significantly reduced lung virus titers (greater than or equal to 2.0 log(10) reduction) when administered 96 h postinfection. Prophylactic administration of 10 mg/kg RSHZ19 was significantly more protective than 1000 mg/kg conventional human immune serum globulin (HSIg), and protective serum-neutralizing titers in MAb-treated animals (1:32, which correlated with approximately 40 mu g/ml determined by anti-idiotype ELISA) were significantly lower than those reported previously for HSIg or for convalescent human serum (1:200-1:400). MAb concentration in lung lavages was determined by ELISA to be approximately 1% of the serum MAE, concentration, but was not detectable by neutralization assay. The degree of lung histopathology in MAb-treated cotton rats was proportional to lung virus titer, and inversely proportional to the RSHZ19 dose administered. There was no evidence of exacerbated disease in the lungs of MAb-treated animals. These studies thus support the potential clinical utility of RSHZ19 MAI, in the prevention and treatment of RSV-induced disease in humans.
引用
收藏
页码:543 / 550
页数:8
相关论文
共 25 条
[1]   CHARACTERIZATION OF 2 ANTIGENIC SITES RECOGNIZED BY NEUTRALIZING MONOCLONAL-ANTIBODIES DIRECTED AGAINST THE FUSION GLYCOPROTEIN OF HUMAN RESPIRATORY SYNCYTIAL VIRUS [J].
ARBIZA, J ;
TAYLOR, G ;
LOPEZ, JA ;
FURZE, J ;
WYLD, S ;
WHYTE, P ;
STOTT, EJ ;
WERTZ, G ;
SULLENDER, W ;
TRUDEL, M ;
MELERO, JA .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :2225-2234
[2]   NEUTRALIZATION EPITOPES OF THE F-GLYCOPROTEIN OF RESPIRATORY SYNCYTIAL VIRUS - EFFECT OF MUTATION UPON FUSION FUNCTION [J].
BEELER, JA ;
COELINGH, KV .
JOURNAL OF VIROLOGY, 1989, 63 (07) :2941-2950
[3]  
Billetta R, 1993, Int Rev Immunol, V10, P165, DOI 10.3109/08830189309061693
[4]  
BRADLEY JS, 1990, ANTIMICROB AGENTS CH, V34, P68
[5]  
CHANOCK RM, 1990, VIROLOGY, P963
[6]  
EVERITT D, 1995, PEDIATR RES, V37, pA173
[7]   RISK OF RESPIRATORY SYNCYTIAL VIRUS-INFECTION FOR INFANTS FROM LOW-INCOME FAMILIES IN RELATIONSHIP TO AGE, SEX, ETHNIC-GROUP, AND MATERNAL ANTIBODY LEVEL [J].
GLEZEN, WP ;
PAREDES, A ;
ALLISON, JE ;
TABER, LH ;
FRANK, AL .
JOURNAL OF PEDIATRICS, 1981, 98 (05) :708-715
[8]   IMMUNOPROPHYLAXIS AND IMMUNOTHERAPY OF RESPIRATORY SYNCYTIAL VIRUS-INFECTED MICE WITH RESPIRATORY SYNCYTIAL VIRUS-SPECIFIC IMMUNE SERUM [J].
GRAHAM, BS ;
DAVIS, TH ;
TANG, YW ;
GRUBER, WC .
PEDIATRIC RESEARCH, 1993, 34 (02) :167-172
[9]   PROPHYLACTIC ADMINISTRATION OF RESPIRATORY SYNCYTIAL VIRUS IMMUNE GLOBULIN TO HIGH-RISK INFANTS AND YOUNG-CHILDREN [J].
GROOTHUIS, JR ;
SIMOES, EAF ;
LEVIN, MJ ;
HALL, CB ;
LONG, CE ;
RODRIGUEZ, WJ ;
ARROBIO, J ;
MEISSNER, HC ;
FULTON, DR ;
WELLIVER, RC ;
TRISTRAM, DA ;
SIBER, GR ;
PRINCE, GA ;
VANRADEN, M ;
HEMMING, VG .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (21) :1524-1530
[10]   INTRAVENOUS IMMUNOGLOBULIN TREATMENT OF RESPIRATORY SYNCYTIAL VIRUS-INFECTIONS IN INFANTS AND YOUNG-CHILDREN [J].
HEMMING, VG ;
RODRIGUEZ, W ;
KIM, HW ;
BRANDT, CD ;
PARROTT, RH ;
BURCH, B ;
PRINCE, GA ;
BARON, PA ;
FINK, RJ ;
REAMAN, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (12) :1882-1886