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A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein
Zika virus (ZIKV) infection poses a serious threat to human health. However, no licensed vaccine or therapeutic drug is currently available for ZIKV. We have previously shown that recombinant ZIKV E80 protein induced potent neutralizing antibody response and protected mice from lethal viral challeng...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997156/ https://www.ncbi.nlm.nih.gov/pubmed/32025335 http://dx.doi.org/10.1038/s41421-019-0140-8 |
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author | Qu, Panke Zhang, Chao Li, Min Ma, Weimin Xiong, Pei Liu, Qingwei Zou, Gang Lavillette, Dimitri Yin, Feifei Jin, Xia Huang, Zhong |
author_facet | Qu, Panke Zhang, Chao Li, Min Ma, Weimin Xiong, Pei Liu, Qingwei Zou, Gang Lavillette, Dimitri Yin, Feifei Jin, Xia Huang, Zhong |
author_sort | Qu, Panke |
collection | PubMed |
description | Zika virus (ZIKV) infection poses a serious threat to human health. However, no licensed vaccine or therapeutic drug is currently available for ZIKV. We have previously shown that recombinant ZIKV E80 protein induced potent neutralizing antibody response and protected mice from lethal viral challenge. In the present study, we isolated five ZIKV neutralizing monoclonal antibodies (mAbs) from E80-immunized mice. These five mAbs specifically bound and neutralized Asian-lineage ZIKV strains. Epitope mapping revealed that all of the five mAbs recognized a novel linear epitope located on the glycan loop of E protein domain I. Sequence alignment revealed that the epitope was extremely conserved in ZIKV but highly variable between ZIKV and other flaviviruses. Thus, these five mAbs form a new class of anti-ZIKV antibodies exhibiting broad-spectrum neutralization on Asian-lineage ZIKV. A representative of this mAb class, 5F8, was found to exert inhibitory function in vitro primarily at the early stage of the post-attachment viral entry process. Importantly, mAb 5F8 was able to confer full protection in a mouse model of ZIKV lethal infection. Our results have strong implications for developing anti-ZIKV vaccines and therapeutic mAbs. |
format | Online Article Text |
id | pubmed-6997156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69971562020-02-05 A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein Qu, Panke Zhang, Chao Li, Min Ma, Weimin Xiong, Pei Liu, Qingwei Zou, Gang Lavillette, Dimitri Yin, Feifei Jin, Xia Huang, Zhong Cell Discov Article Zika virus (ZIKV) infection poses a serious threat to human health. However, no licensed vaccine or therapeutic drug is currently available for ZIKV. We have previously shown that recombinant ZIKV E80 protein induced potent neutralizing antibody response and protected mice from lethal viral challenge. In the present study, we isolated five ZIKV neutralizing monoclonal antibodies (mAbs) from E80-immunized mice. These five mAbs specifically bound and neutralized Asian-lineage ZIKV strains. Epitope mapping revealed that all of the five mAbs recognized a novel linear epitope located on the glycan loop of E protein domain I. Sequence alignment revealed that the epitope was extremely conserved in ZIKV but highly variable between ZIKV and other flaviviruses. Thus, these five mAbs form a new class of anti-ZIKV antibodies exhibiting broad-spectrum neutralization on Asian-lineage ZIKV. A representative of this mAb class, 5F8, was found to exert inhibitory function in vitro primarily at the early stage of the post-attachment viral entry process. Importantly, mAb 5F8 was able to confer full protection in a mouse model of ZIKV lethal infection. Our results have strong implications for developing anti-ZIKV vaccines and therapeutic mAbs. Nature Publishing Group UK 2020-02-04 /pmc/articles/PMC6997156/ /pubmed/32025335 http://dx.doi.org/10.1038/s41421-019-0140-8 Text en © The Author(s) 2020 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 Qu, Panke Zhang, Chao Li, Min Ma, Weimin Xiong, Pei Liu, Qingwei Zou, Gang Lavillette, Dimitri Yin, Feifei Jin, Xia Huang, Zhong A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title | A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title_full | A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title_fullStr | A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title_full_unstemmed | A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title_short | A new class of broadly neutralizing antibodies that target the glycan loop of Zika virus envelope protein |
title_sort | new class of broadly neutralizing antibodies that target the glycan loop of zika virus envelope protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997156/ https://www.ncbi.nlm.nih.gov/pubmed/32025335 http://dx.doi.org/10.1038/s41421-019-0140-8 |
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