Characterization of a Novel Neutralizing Monoclonal Antibody Against Ebola Virus GP

被引:18
|
作者
Reynard, Olivier [1 ]
Volchkov, Viktor E. [1 ]
机构
[1] Univ Lyon 1, Ecole Normale Super Lyon, CNRS UMR5308, INSERM U1111,CIRI,Mol Basis Viral Pathogen, F-69365 Lyon 07, France
来源
JOURNAL OF INFECTIOUS DISEASES | 2015年 / 212卷
关键词
Ebola virus; glycoprotein GP; virus neutralizing antibody; filovirus; DISTINCT MECHANISMS; HEMORRHAGIC-FEVER; GLYCOPROTEIN GP; ENTRY REQUIRES; MARBURG VIRUS; INFECTION; GENE; REPLICATION; ZAIRE; PROTEOLYSIS;
D O I
10.1093/infdis/jiv303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ebola virus is the etiological agent of a severe hemorrhagic fever with a high mortality rate. As the only protein exposed on the surface of viral particles, the spike glycoprotein GP is the unique target for neutralizing monoclonal antibodies. In this study, we demonstrate the strong neutralization capacity of the monoclonal antibody #3327 and characterize its activity. GP residues that are required for recognition and neutralization were found to be located both in the internal fusion loop and in the receptor-binding domain. Analysis of Ebola virus entry in the presence of #3327 allows us to hypothesize that this antibody binds to the virus particle before internalization and endosomal processing of GP and likely prevents the final viral fusion step. Importantly, #3327 is able to block entry of virions bearing GP that contain the Q508 escape mutation common to a number of virus-neutralizing antibodies, and therefore provides future perspectives for treatment strategies against Ebola virus infection.
引用
收藏
页码:S372 / S378
页数:7
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