Clinical Potential of Prefusion RSV F-specific Antibodies

病毒学 生物 抗体 病毒 病毒进入 单克隆抗体 表位 中和抗体 脂质双层融合 维罗细胞 免疫学 病毒复制
作者
Iebe Rossey,Jason S. McLellan,Xavier Saelens,Bert Schepens
出处
期刊:Trends in Microbiology [Elsevier BV]
卷期号:26 (3): 209-219 被引量:61
标识
DOI:10.1016/j.tim.2017.09.009
摘要

Most of the RSV-neutralizing activity in human serum is conferred by antibodies that specifically bind to prefusion F. The RSV-neutralizing activity of an antibody correlates with its affinity for prefusion F. The epitope of F-binding antibodies is often not restricted to one site. An increasing number of RSV F-specific monoclonal antibodies have been described, a few of which even neutralize closely related pneumoviruses. 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. 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.
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