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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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