Clinical Potential of Prefusion RSV F-specific Antibodies

被引:53
作者
Rossey, Iebe [1 ,2 ]
McLellan, Jason S. [3 ]
Saelens, Xavier [1 ,2 ]
Schepens, Bert [1 ,2 ]
机构
[1] VIB UGent Ctr Med Biotechnol, Technol Pk 927, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9052 Ghent, Belgium
[3] Geisel Sch Med Dartmouth, Dept Biochem & Cell Biol, Hanover, NH 03755 USA
关键词
RESPIRATORY SYNCYTIAL VIRUS; HUMANIZED MONOCLONAL-ANTIBODY; FUSION-GLYCOPROTEIN VACCINE; HIGH-RISK CHILDREN; STRUCTURAL BASIS; VIRAL LOAD; INFECTION; PROTEIN; NEUTRALIZATION; MOTAVIZUMAB;
D O I
10.1016/j.tim.2017.09.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human respiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infections in the very young. The RSV fusion protein (F) is essential for virus entry because it mediates viral and host membrane fusion. During this fusion process F is converted from a metastable prefusion conformation into an energetically favored postfusion state. Antibodies that target F can prevent viral entry and reduce disease caused by RSV. During recent years, many prefusion F-specific antibodies have been described. These antibodies typically have stronger RSV-neutralizing activity compared to those that also bind F in the postfusion conformation. Here, we describe how F-specific antibodies protect against RSV and why specifically targeting prefusion F could have great clinical potential.
引用
收藏
页码:209 / 219
页数:11
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