Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.
Nat Rev Microbiol. 2019 Apr;17(4):233-245. doi: 10.1038/s41579-019-0149-x.
Respiratory syncytial virus (RSV) is a leading cause of lower respiratory tract disease in young children and elderly people. Although the virus was isolated in 1955, an effective RSV vaccine has not been developed, and the only licensed intervention is passive immunoprophylaxis of high-risk infants with a humanized monoclonal antibody. During the past 5 years, however, there has been substantial progress in our understanding of the structure and function of the RSV glycoproteins and their interactions with host cell factors that mediate entry. This period has coincided with renewed interest in developing effective interventions, including the isolation of potent monoclonal antibodies and small molecules and the design of novel vaccine candidates. In this Review, we summarize the recent findings that have begun to elucidate RSV entry mechanisms, describe progress on the development of new interventions and conclude with a perspective on gaps in our knowledge that require further investigation.
呼吸道合胞病毒(RSV)是导致婴幼儿和老年人下呼吸道疾病的主要原因。尽管该病毒于 1955 年被分离出来,但尚未开发出有效的 RSV 疫苗,唯一获得许可的干预措施是用一种人源化单克隆抗体对高危婴儿进行被动免疫预防。然而,在过去的 5 年中,我们对 RSV 糖蛋白的结构和功能及其与介导进入的宿主细胞因子的相互作用有了更深入的了解。这一时期恰逢人们重新产生开发有效干预措施的兴趣,包括分离强效单克隆抗体和小分子,以及设计新型疫苗候选物。在这篇综述中,我们总结了最近的发现,这些发现开始阐明 RSV 进入机制,描述了新干预措施的进展,并就我们需要进一步研究的知识空白提出了看法。