Respiratory syncytial virus entry and how to block it

被引:245
作者
Battles, Michael B. [1 ]
McLellan, Jason S. [2 ]
机构
[1] Geisel Sch Med Dartmouth, Dept Biochem & Cell Biol, Hanover, NH USA
[2] Univ Texas Austin, Dept Mol Biosci, Austin, TX 78712 USA
关键词
ATTACHMENT PROTEIN-G; ANTIBODY-MEDIATED RESTRICTION; CENTRAL CONSERVED REGION; FUSION F GLYCOPROTEIN; CORYZA AGENT CCA; NF-KAPPA-B; HUMAN METAPNEUMOVIRUS; MATRIX PROTEIN; SOLUBLE FORM; 60-NUCLEOTIDE DUPLICATION;
D O I
10.1038/s41579-019-0149-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:233 / 245
页数:13
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