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Respiratory syncytial virus entry and how to block it

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...

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Autores principales: Battles, Michael B., McLellan, Jason S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096974/
https://www.ncbi.nlm.nih.gov/pubmed/30723301
http://dx.doi.org/10.1038/s41579-019-0149-x
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author Battles, Michael B.
McLellan, Jason S.
author_facet Battles, Michael B.
McLellan, Jason S.
author_sort Battles, Michael B.
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description 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.
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spelling pubmed-70969742020-03-26 Respiratory syncytial virus entry and how to block it Battles, Michael B. McLellan, Jason S. Nat Rev Microbiol Review Article 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. Nature Publishing Group UK 2019-02-05 2019 /pmc/articles/PMC7096974/ /pubmed/30723301 http://dx.doi.org/10.1038/s41579-019-0149-x Text en © Springer Nature Limited 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Battles, Michael B.
McLellan, Jason S.
Respiratory syncytial virus entry and how to block it
title Respiratory syncytial virus entry and how to block it
title_full Respiratory syncytial virus entry and how to block it
title_fullStr Respiratory syncytial virus entry and how to block it
title_full_unstemmed Respiratory syncytial virus entry and how to block it
title_short Respiratory syncytial virus entry and how to block it
title_sort respiratory syncytial virus entry and how to block it
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7096974/
https://www.ncbi.nlm.nih.gov/pubmed/30723301
http://dx.doi.org/10.1038/s41579-019-0149-x
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