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Enterovirus A71 antivirals: Past, present, and future
Enterovirus A71 (EV-A71) is a significant human pathogen, especially in children. EV-A71 infection is one of the leading causes of hand, foot, and mouth diseases (HFMD), and can lead to neurological complications such as acute flaccid myelitis (AFM) in severe cases. Although three EV-A71 vaccines ar...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279511/ https://www.ncbi.nlm.nih.gov/pubmed/35847514 http://dx.doi.org/10.1016/j.apsb.2021.08.017 |
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author | Wang, Jun Hu, Yanmei Zheng, Madeleine |
author_facet | Wang, Jun Hu, Yanmei Zheng, Madeleine |
author_sort | Wang, Jun |
collection | PubMed |
description | Enterovirus A71 (EV-A71) is a significant human pathogen, especially in children. EV-A71 infection is one of the leading causes of hand, foot, and mouth diseases (HFMD), and can lead to neurological complications such as acute flaccid myelitis (AFM) in severe cases. Although three EV-A71 vaccines are available in China, they are not broadly protective and have reduced efficacy against emerging strains. There is currently no approved antiviral for EV-A71. Significant progress has been made in developing antivirals against EV-A71 by targeting both viral proteins and host factors. However, viral capsid inhibitors and protease inhibitors failed in clinical trials of human rhinovirus infection due to limited efficacy or side effects. This review discusses major discoveries in EV-A71 antiviral development, analyzes the advantages and limitations of each drug target, and highlights the knowledge gaps that need to be addressed to advance the field forward. |
format | Online Article Text |
id | pubmed-9279511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92795112022-07-15 Enterovirus A71 antivirals: Past, present, and future Wang, Jun Hu, Yanmei Zheng, Madeleine Acta Pharm Sin B Review Enterovirus A71 (EV-A71) is a significant human pathogen, especially in children. EV-A71 infection is one of the leading causes of hand, foot, and mouth diseases (HFMD), and can lead to neurological complications such as acute flaccid myelitis (AFM) in severe cases. Although three EV-A71 vaccines are available in China, they are not broadly protective and have reduced efficacy against emerging strains. There is currently no approved antiviral for EV-A71. Significant progress has been made in developing antivirals against EV-A71 by targeting both viral proteins and host factors. However, viral capsid inhibitors and protease inhibitors failed in clinical trials of human rhinovirus infection due to limited efficacy or side effects. This review discusses major discoveries in EV-A71 antiviral development, analyzes the advantages and limitations of each drug target, and highlights the knowledge gaps that need to be addressed to advance the field forward. Elsevier 2022-04 2021-08-20 /pmc/articles/PMC9279511/ /pubmed/35847514 http://dx.doi.org/10.1016/j.apsb.2021.08.017 Text en © 2022 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Review Wang, Jun Hu, Yanmei Zheng, Madeleine Enterovirus A71 antivirals: Past, present, and future |
title | Enterovirus A71 antivirals: Past, present, and future |
title_full | Enterovirus A71 antivirals: Past, present, and future |
title_fullStr | Enterovirus A71 antivirals: Past, present, and future |
title_full_unstemmed | Enterovirus A71 antivirals: Past, present, and future |
title_short | Enterovirus A71 antivirals: Past, present, and future |
title_sort | enterovirus a71 antivirals: past, present, and future |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279511/ https://www.ncbi.nlm.nih.gov/pubmed/35847514 http://dx.doi.org/10.1016/j.apsb.2021.08.017 |
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