VIB-UGent Center for Medical Biotechnology, Technologiepark 927, Ghent, B-9052, Belgium; Department of Biomedical Molecular Biology, Ghent University, Ghent, B-9052, Belgium.
Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755-3844, USA.
Trends Microbiol. 2018 Mar;26(3):209-219. doi: 10.1016/j.tim.2017.09.009. Epub 2017 Oct 17.
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.
人呼吸道合胞病毒(RSV)是导致非常年幼的人下呼吸道感染的主要原因。RSV 融合蛋白(F)对于病毒进入至关重要,因为它介导病毒和宿主膜融合。在这个融合过程中,F 从亚稳定的预融合构象转化为能量有利的融合后状态。针对 F 的抗体可以预防病毒进入并减少 RSV 引起的疾病。近年来,已经描述了许多预融合 F 特异性抗体。与那些也结合融合后构象中的 F 的抗体相比,这些抗体通常具有更强的 RSV 中和活性。在这里,我们描述了 F 特异性抗体如何预防 RSV 以及为什么特别针对预融合 F 可能具有巨大的临床潜力。