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A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III
Dengue is the most widespread vector-borne viral disease caused by dengue virus (DENV) for which there are no safe, effective drugs approved for clinical use. Here, by using sequential antigen panning of a yeast antibody library derived from healthy donors against the DENV envelop protein domain III...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615639/ https://www.ncbi.nlm.nih.gov/pubmed/31242272 http://dx.doi.org/10.1371/journal.ppat.1007836 |
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author | Hu, Dan Zhu, Zhongyu Li, Shun Deng, Yongqiang Wu, Yanling Zhang, Nana Puri, Vinita Wang, Chunyu Zou, Peng Lei, Cheng Tian, Xiaolong Wang, Yulu Zhao, Qi Li, Wei Prabakaran, Ponraj Feng, Yang Cardosa, Jane Qin, Chengfeng Zhou, Xiaohui Dimitrov, Dimiter S. Ying, Tianlei |
author_facet | Hu, Dan Zhu, Zhongyu Li, Shun Deng, Yongqiang Wu, Yanling Zhang, Nana Puri, Vinita Wang, Chunyu Zou, Peng Lei, Cheng Tian, Xiaolong Wang, Yulu Zhao, Qi Li, Wei Prabakaran, Ponraj Feng, Yang Cardosa, Jane Qin, Chengfeng Zhou, Xiaohui Dimitrov, Dimiter S. Ying, Tianlei |
author_sort | Hu, Dan |
collection | PubMed |
description | Dengue is the most widespread vector-borne viral disease caused by dengue virus (DENV) for which there are no safe, effective drugs approved for clinical use. Here, by using sequential antigen panning of a yeast antibody library derived from healthy donors against the DENV envelop protein domain III (DIII) combined with depletion by an entry defective DIII mutant, we identified a cross-reactive human monoclonal antibody (mAb), m366.6, which bound with high affinity to DENV DIII from all four DENV serotypes. Immunogenetic analysis indicated that m366.6 is a germline-like mAb with very few somatic mutations from the closest VH and Vλ germline genes. Importantly, we demonstrated that it potently neutralized DENV both in vitro and in the mouse models of DENV infection without detectable antibody-dependent enhancement (ADE) effect. The epitope of m366.6 was mapped to the highly conserved regions on DIII, which may guide the design of effective dengue vaccine immunogens. Furthermore, as the first germline-like mAb derived from a naïve antibody library that could neutralize all four DENV serotypes, the m366.6 can be a tool for exploring mechanisms of DENV infection, and is a promising therapeutic candidate. |
format | Online Article Text |
id | pubmed-6615639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-66156392019-07-25 A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III Hu, Dan Zhu, Zhongyu Li, Shun Deng, Yongqiang Wu, Yanling Zhang, Nana Puri, Vinita Wang, Chunyu Zou, Peng Lei, Cheng Tian, Xiaolong Wang, Yulu Zhao, Qi Li, Wei Prabakaran, Ponraj Feng, Yang Cardosa, Jane Qin, Chengfeng Zhou, Xiaohui Dimitrov, Dimiter S. Ying, Tianlei PLoS Pathog Research Article Dengue is the most widespread vector-borne viral disease caused by dengue virus (DENV) for which there are no safe, effective drugs approved for clinical use. Here, by using sequential antigen panning of a yeast antibody library derived from healthy donors against the DENV envelop protein domain III (DIII) combined with depletion by an entry defective DIII mutant, we identified a cross-reactive human monoclonal antibody (mAb), m366.6, which bound with high affinity to DENV DIII from all four DENV serotypes. Immunogenetic analysis indicated that m366.6 is a germline-like mAb with very few somatic mutations from the closest VH and Vλ germline genes. Importantly, we demonstrated that it potently neutralized DENV both in vitro and in the mouse models of DENV infection without detectable antibody-dependent enhancement (ADE) effect. The epitope of m366.6 was mapped to the highly conserved regions on DIII, which may guide the design of effective dengue vaccine immunogens. Furthermore, as the first germline-like mAb derived from a naïve antibody library that could neutralize all four DENV serotypes, the m366.6 can be a tool for exploring mechanisms of DENV infection, and is a promising therapeutic candidate. Public Library of Science 2019-06-26 /pmc/articles/PMC6615639/ /pubmed/31242272 http://dx.doi.org/10.1371/journal.ppat.1007836 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Hu, Dan Zhu, Zhongyu Li, Shun Deng, Yongqiang Wu, Yanling Zhang, Nana Puri, Vinita Wang, Chunyu Zou, Peng Lei, Cheng Tian, Xiaolong Wang, Yulu Zhao, Qi Li, Wei Prabakaran, Ponraj Feng, Yang Cardosa, Jane Qin, Chengfeng Zhou, Xiaohui Dimitrov, Dimiter S. Ying, Tianlei A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title | A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title_full | A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title_fullStr | A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title_full_unstemmed | A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title_short | A broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain III |
title_sort | broadly neutralizing germline-like human monoclonal antibody against dengue virus envelope domain iii |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615639/ https://www.ncbi.nlm.nih.gov/pubmed/31242272 http://dx.doi.org/10.1371/journal.ppat.1007836 |
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