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Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children
Protective antibody levels are critical for protection from severe enterovirus 71 infection. However, little is known about the specificities and functional properties of the enterovirus 71-specific antibodies induced by natural infection in humans. Here we characterize 191 plasmablast-derived monoc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624920/ https://www.ncbi.nlm.nih.gov/pubmed/28970483 http://dx.doi.org/10.1038/s41467-017-00736-9 |
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author | Arthur Huang, Kuan-Ying Chen, Mei-Feng Huang, Yhu-Chering Shih, Shin-Ru Chiu, Cheng-Hsun Lin, Jainn-Jim Wang, Jen-Ren Tsao, Kuo-Chien Lin, Tzou-Yien |
author_facet | Arthur Huang, Kuan-Ying Chen, Mei-Feng Huang, Yhu-Chering Shih, Shin-Ru Chiu, Cheng-Hsun Lin, Jainn-Jim Wang, Jen-Ren Tsao, Kuo-Chien Lin, Tzou-Yien |
author_sort | Arthur Huang, Kuan-Ying |
collection | PubMed |
description | Protective antibody levels are critical for protection from severe enterovirus 71 infection. However, little is known about the specificities and functional properties of the enterovirus 71-specific antibodies induced by natural infection in humans. Here we characterize 191 plasmablast-derived monoclonal antibodies from three enterovirus 71-infected children, each of whom shows a distinct serological response. Of the 84 enterovirus 71-specific antibodies, neutralizing antibodies that target the rims and floor of the capsid canyon exhibit broad and potent activities at the nanogram level against viruses isolated in 1998–2016. We also find a subset of infected children whose enterovirus 71-specific antibodies are focused on the 3- and 2-fold plateau epitopes localized at the margin of pentamers, and this type of antibody response is associated with lower serum titers against recently circulating strains. Our data provide new insights into the enterovirus 71-specific antibodies induced by natural infection at the serological and clonal levels. |
format | Online Article Text |
id | pubmed-5624920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56249202017-10-04 Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children Arthur Huang, Kuan-Ying Chen, Mei-Feng Huang, Yhu-Chering Shih, Shin-Ru Chiu, Cheng-Hsun Lin, Jainn-Jim Wang, Jen-Ren Tsao, Kuo-Chien Lin, Tzou-Yien Nat Commun Article Protective antibody levels are critical for protection from severe enterovirus 71 infection. However, little is known about the specificities and functional properties of the enterovirus 71-specific antibodies induced by natural infection in humans. Here we characterize 191 plasmablast-derived monoclonal antibodies from three enterovirus 71-infected children, each of whom shows a distinct serological response. Of the 84 enterovirus 71-specific antibodies, neutralizing antibodies that target the rims and floor of the capsid canyon exhibit broad and potent activities at the nanogram level against viruses isolated in 1998–2016. We also find a subset of infected children whose enterovirus 71-specific antibodies are focused on the 3- and 2-fold plateau epitopes localized at the margin of pentamers, and this type of antibody response is associated with lower serum titers against recently circulating strains. Our data provide new insights into the enterovirus 71-specific antibodies induced by natural infection at the serological and clonal levels. Nature Publishing Group UK 2017-10-02 /pmc/articles/PMC5624920/ /pubmed/28970483 http://dx.doi.org/10.1038/s41467-017-00736-9 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Arthur Huang, Kuan-Ying Chen, Mei-Feng Huang, Yhu-Chering Shih, Shin-Ru Chiu, Cheng-Hsun Lin, Jainn-Jim Wang, Jen-Ren Tsao, Kuo-Chien Lin, Tzou-Yien Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title | Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title_full | Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title_fullStr | Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title_full_unstemmed | Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title_short | Epitope-associated and specificity-focused features of EV71-neutralizing antibody repertoires from plasmablasts of infected children |
title_sort | epitope-associated and specificity-focused features of ev71-neutralizing antibody repertoires from plasmablasts of infected children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624920/ https://www.ncbi.nlm.nih.gov/pubmed/28970483 http://dx.doi.org/10.1038/s41467-017-00736-9 |
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