Nanobodies® Specific for Respiratory Syncytial Virus Fusion Protein Protect Against Infection by Inhibition of Fusion

被引:41
|
作者
Schepens, Bert [1 ,2 ]
Ibanez, Lorena Itati [1 ,2 ]
De Baets, Sarah [1 ,2 ]
Hultberg, Anna [3 ]
Bogaert, Pieter [1 ,2 ]
De Bleser, Pieter [1 ,2 ]
Vervalle, Frederik [1 ,2 ]
Verrips, Theo [3 ]
Melero, Jose [4 ,5 ]
Vandevelde, Wesly [6 ]
Vanlandschoot, Peter [6 ]
Saelens, Xavier [1 ,2 ]
机构
[1] Univ Ghent VIB, Dept Mol Biomed Res, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, Ghent, Belgium
[3] Univ Utrecht, Dept Biol, NL-3508 TC Utrecht, Netherlands
[4] Inst Salud Carlos III, Ctr Nacl Microbiol, Madrid 28220, Spain
[5] Inst Salud Carlos III, CIBER Enfermedades Resp, Madrid 28220, Spain
[6] Ablynx NV, B-9052 Ghent, Belgium
来源
JOURNAL OF INFECTIOUS DISEASES | 2011年 / 204卷 / 11期
关键词
REPLICATION IN-VITRO; STRUCTURAL BASIS; ANTIBODIES; GLYCOPROTEIN; NEUTRALIZATION; INFANTS; FORMS;
D O I
10.1093/infdis/jir622
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the medical importance of respiratory syncytial virus (RSV) infections, there is no vaccine or therapeutic agent available. Prophylactic administration of palivizumab, a humanized monoclonal RSV fusion (F) protein-specific antibody, can protect high-risk children. Previously, we have demonstrated that RSV can be neutralized by picomolar concentrations of a camelid immunoglobulin single-variable domain that binds the RSV protein F (F-VHHb nanobodies). Here, we investigated the mechanism by which these nanobodies neutralize RSV and tested their antiviral activity in vivo. We demonstrate that bivalent RSV F-specific nanobodies neutralize RSV infection by inhibiting fusion without affecting viral attachment. The ability of RSV F-specific nanobodies to protect against RSV infection was investigated in vivo. Intranasal administration of bivalent RSV F-specific nanobodies protected BALB/c mice from RSV infection, and associated pulmonary inflammation. Moreover, therapeutic treatment with these nanobodies after RSV infection could reduce viral replication and reduced pulmonary inflammation. Thus, nanobodies are promising therapeutic molecules for treatment of RSV.
引用
收藏
页码:1692 / 1701
页数:10
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