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Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development

BACKGROUND: Recently, enterovirus 71 (EV71) has caused life-threatening outbreaks involving neurological and cardiopulmonary complications in Asian children with unknown mechanism. EV71 has one single serotype but can be phylogenetically classified into 3 main genogroups (A, B and C) and 11 genotype...

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Autores principales: Huang, Mei-Liang, Chiang, Pai-Shan, Chia, Min-Yuan, Luo, Shu-Ting, Chang, Luan-Yin, Lin, Tzou-Yien, Ho, Mei-Shang, Lee, Min-Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573098/
https://www.ncbi.nlm.nih.gov/pubmed/23459633
http://dx.doi.org/10.1371/journal.pntd.0002067
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author Huang, Mei-Liang
Chiang, Pai-Shan
Chia, Min-Yuan
Luo, Shu-Ting
Chang, Luan-Yin
Lin, Tzou-Yien
Ho, Mei-Shang
Lee, Min-Shi
author_facet Huang, Mei-Liang
Chiang, Pai-Shan
Chia, Min-Yuan
Luo, Shu-Ting
Chang, Luan-Yin
Lin, Tzou-Yien
Ho, Mei-Shang
Lee, Min-Shi
author_sort Huang, Mei-Liang
collection PubMed
description BACKGROUND: Recently, enterovirus 71 (EV71) has caused life-threatening outbreaks involving neurological and cardiopulmonary complications in Asian children with unknown mechanism. EV71 has one single serotype but can be phylogenetically classified into 3 main genogroups (A, B and C) and 11 genotypes (A, B1∼B5 and C1∼C5). In Taiwan, nationwide EV71 epidemics with different predominant genotypes occurred in 1998 (C2), 2000–2001 (B4), 2004–2005 (C4), and 2008 (B5). In this study, sera were collected to measure cross-reactive neutralizing antibody titers against different genotypes. METHODS: We collected historical sera from children who developed an EV71 infection in 1998, 2000, 2005, 2008, or 2010 and measured cross-reactive neutralizing antibody titers against all 11 EV71 genotypes. In addition, we aligned and compared the amino acid sequences of P1 proteins of the tested viruses. RESULTS: Serology data showed that children infected with genogroups B and C consistently have lower neutralizing antibody titers against genogroup A (>4-fold difference). The sequence comparisons revealed that five amino acid signatures (N143D in VP2; K18R, H116Y, D167E, and S275A in VP1) are specific for genogroup A and may be related to the observed antigenic variations. CONCLUSIONS: This study documented antigenic variations among different EV71 genogroups and identified potential immunodominant amino acid positions. Enterovirus surveillance and vaccine development should monitor these positions.
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spelling pubmed-35730982013-03-01 Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development Huang, Mei-Liang Chiang, Pai-Shan Chia, Min-Yuan Luo, Shu-Ting Chang, Luan-Yin Lin, Tzou-Yien Ho, Mei-Shang Lee, Min-Shi PLoS Negl Trop Dis Research Article BACKGROUND: Recently, enterovirus 71 (EV71) has caused life-threatening outbreaks involving neurological and cardiopulmonary complications in Asian children with unknown mechanism. EV71 has one single serotype but can be phylogenetically classified into 3 main genogroups (A, B and C) and 11 genotypes (A, B1∼B5 and C1∼C5). In Taiwan, nationwide EV71 epidemics with different predominant genotypes occurred in 1998 (C2), 2000–2001 (B4), 2004–2005 (C4), and 2008 (B5). In this study, sera were collected to measure cross-reactive neutralizing antibody titers against different genotypes. METHODS: We collected historical sera from children who developed an EV71 infection in 1998, 2000, 2005, 2008, or 2010 and measured cross-reactive neutralizing antibody titers against all 11 EV71 genotypes. In addition, we aligned and compared the amino acid sequences of P1 proteins of the tested viruses. RESULTS: Serology data showed that children infected with genogroups B and C consistently have lower neutralizing antibody titers against genogroup A (>4-fold difference). The sequence comparisons revealed that five amino acid signatures (N143D in VP2; K18R, H116Y, D167E, and S275A in VP1) are specific for genogroup A and may be related to the observed antigenic variations. CONCLUSIONS: This study documented antigenic variations among different EV71 genogroups and identified potential immunodominant amino acid positions. Enterovirus surveillance and vaccine development should monitor these positions. Public Library of Science 2013-02-14 /pmc/articles/PMC3573098/ /pubmed/23459633 http://dx.doi.org/10.1371/journal.pntd.0002067 Text en © 2013 Huang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Huang, Mei-Liang
Chiang, Pai-Shan
Chia, Min-Yuan
Luo, Shu-Ting
Chang, Luan-Yin
Lin, Tzou-Yien
Ho, Mei-Shang
Lee, Min-Shi
Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title_full Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title_fullStr Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title_full_unstemmed Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title_short Cross-reactive Neutralizing Antibody Responses to Enterovirus 71 Infections in Young Children: Implications for Vaccine Development
title_sort cross-reactive neutralizing antibody responses to enterovirus 71 infections in young children: implications for vaccine development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3573098/
https://www.ncbi.nlm.nih.gov/pubmed/23459633
http://dx.doi.org/10.1371/journal.pntd.0002067
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