CORRELATION BETWEEN THE REACTIVITY PATTERNS OF MONOCLONAL-ANTIBODIES TO DISTINCT ANTIGENIC SITES ON HN GLYCOPROTEIN AND THEIR PROTECTIVE ABILITIES IN SENDAI (6/94) VIRUS-INFECTION

被引:4
作者
PIGA, N [1 ]
KESSLER, N [1 ]
LAYANI, MP [1 ]
AYMARD, M [1 ]
机构
[1] UNIV CLAUDE BERNARD LYON 1,VIROL LAB,8 AVE ROCKEFELLER,F-69373 LYONS 08,FRANCE
关键词
D O I
10.1007/BF01311287
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The relative importance of the host immune response to various antigenic and functional sites on the HN glycoprotein of Sendai (6/94) virus for protection in vivo, was evaluated in mice passively immunized with monoclonal antibodies to HN and then intranasally challenged with infectious virus. Five neutralizing monoclonal antibodies reacting with distinct antigenic sites and exhibiting different reactivity patterns were selected. All of them were able to prevent entirely the growth of virus in the lungs of experimental animals injected with appropriate dilutions of monoclonal antibody. The calculation of correlation coefficients between the reduction of virus in the lungs of immunized mice and the amount of antibody, expressed in terms of hemagglutination inhibition, hemolysis inhibition or neutralizing units, showed a high degree of correlation (r=0.89) with neutralization and a lack of correlation (r=0.44) with hemagglutination inhibition. In parallel a minimum threshold value for protection equivalent to 2×103 neutralizing units per mouse was determined independently of the mechanism(s) by which monoclonal antibodies mediated the neutralization of the infectivity. On the HN glycoprotein of Sendai (6/94) virus we could not individualize a critical site for successful immune recognition by antibodies although the characteristics of an "ideal protective monoclonal antibody" have also been defined. © 1990 Springer-Verlag.
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页码:179 / 193
页数:15
相关论文
共 22 条
[1]  
BERAUD F, 1984, DEV BIOLOGICALS, V57, P257
[4]   MONOCLONAL-ANTIBODIES TO NEWCASTLE-DISEASE VIRUS - DELINEATION OF 4 EPITOPES ON THE HN GLYCOPROTEIN [J].
IORIO, RM ;
BRATT, MA .
JOURNAL OF VIROLOGY, 1983, 48 (02) :440-450
[5]  
KESSLER N, 1977, J GEN VIROL, V37, P547, DOI 10.1099/0022-1317-37-3-547
[6]   STUDY OF A NEW STRAIN OF PARAMYXOVIRUSES ISOLATED FROM WILD DUCKS - ANTIGENIC AND BIOLOGICAL PROPERTIES [J].
KESSLER, N ;
AYMARD, M ;
CALVET, A .
JOURNAL OF GENERAL VIROLOGY, 1979, 43 (MAY) :273-282
[7]  
KESSLER N, 1983, 4EME C FRANC GRIPP P, P45
[8]   IMPORTANCE OF ANTIBODIES TO THE FUSION GLYCOPROTEIN OF PARAMYXOVIRUSES IN THE PREVENTION OF SPREAD OF INFECTION [J].
MERZ, DC ;
SCHEID, A ;
CHOPPIN, PW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 151 (02) :275-288
[9]   EXPRESSION OF THE F-GLYCOPROTEIN OF RESPIRATORY SYNCYTIAL VIRUS BY A RECOMBINANT VACCINIA VIRUS - COMPARISON OF THE INDIVIDUAL CONTRIBUTIONS OF THE F-GLYCOPROTEIN AND G-GLYCOPROTEIN TO HOST IMMUNITY [J].
OLMSTED, RA ;
ELANGO, N ;
PRINCE, GA ;
MURPHY, BR ;
JOHNSON, PR ;
MOSS, B ;
CHANOCK, RM ;
COLLINS, PL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (19) :7462-7466
[10]  
ORVELL C, 1982, J IMMUNOL, V129, P2779