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High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries

Pandemic and epidemic outbreaks of influenza A virus (IAV) infection pose severe challenges to human society. Passive immunotherapy with recombinant neutralizing antibodies can potentially mitigate the threats of IAV infection. With a high throughput neutralizing antibody discovery platform, we prod...

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Autores principales: Chen, Ing-Chien, Chiu, Yi-Kai, Yu, Chung-Ming, Lee, Cheng-Chung, Tung, Chao-Ping, Tsou, Yueh-Liang, Huang, Yi-Jen, Lin, Chia-Lung, Chen, Hong-Sen, Wang, Andrew H.-J., Yang, An-Suei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663709/
https://www.ncbi.nlm.nih.gov/pubmed/29089574
http://dx.doi.org/10.1038/s41598-017-14823-w
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author Chen, Ing-Chien
Chiu, Yi-Kai
Yu, Chung-Ming
Lee, Cheng-Chung
Tung, Chao-Ping
Tsou, Yueh-Liang
Huang, Yi-Jen
Lin, Chia-Lung
Chen, Hong-Sen
Wang, Andrew H.-J.
Yang, An-Suei
author_facet Chen, Ing-Chien
Chiu, Yi-Kai
Yu, Chung-Ming
Lee, Cheng-Chung
Tung, Chao-Ping
Tsou, Yueh-Liang
Huang, Yi-Jen
Lin, Chia-Lung
Chen, Hong-Sen
Wang, Andrew H.-J.
Yang, An-Suei
author_sort Chen, Ing-Chien
collection PubMed
description Pandemic and epidemic outbreaks of influenza A virus (IAV) infection pose severe challenges to human society. Passive immunotherapy with recombinant neutralizing antibodies can potentially mitigate the threats of IAV infection. With a high throughput neutralizing antibody discovery platform, we produced artificial anti-hemagglutinin (HA) IAV-neutralizing IgGs from phage-displayed synthetic scFv libraries without necessitating prior memory of antibody-antigen interactions or relying on affinity maturation essential for in vivo immune systems to generate highly specific neutralizing antibodies. At least two thirds of the epitope groups of the artificial anti-HA antibodies resemble those of natural protective anti-HA antibodies, providing alternatives to neutralizing antibodies from natural antibody repertoires. With continuing advancement in designing and constructing synthetic scFv libraries, this technological platform is useful in mitigating not only the threats of IAV pandemics but also those from other newly emerging viral infections.
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spelling pubmed-56637092017-11-08 High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries Chen, Ing-Chien Chiu, Yi-Kai Yu, Chung-Ming Lee, Cheng-Chung Tung, Chao-Ping Tsou, Yueh-Liang Huang, Yi-Jen Lin, Chia-Lung Chen, Hong-Sen Wang, Andrew H.-J. Yang, An-Suei Sci Rep Article Pandemic and epidemic outbreaks of influenza A virus (IAV) infection pose severe challenges to human society. Passive immunotherapy with recombinant neutralizing antibodies can potentially mitigate the threats of IAV infection. With a high throughput neutralizing antibody discovery platform, we produced artificial anti-hemagglutinin (HA) IAV-neutralizing IgGs from phage-displayed synthetic scFv libraries without necessitating prior memory of antibody-antigen interactions or relying on affinity maturation essential for in vivo immune systems to generate highly specific neutralizing antibodies. At least two thirds of the epitope groups of the artificial anti-HA antibodies resemble those of natural protective anti-HA antibodies, providing alternatives to neutralizing antibodies from natural antibody repertoires. With continuing advancement in designing and constructing synthetic scFv libraries, this technological platform is useful in mitigating not only the threats of IAV pandemics but also those from other newly emerging viral infections. Nature Publishing Group UK 2017-10-31 /pmc/articles/PMC5663709/ /pubmed/29089574 http://dx.doi.org/10.1038/s41598-017-14823-w 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
Chen, Ing-Chien
Chiu, Yi-Kai
Yu, Chung-Ming
Lee, Cheng-Chung
Tung, Chao-Ping
Tsou, Yueh-Liang
Huang, Yi-Jen
Lin, Chia-Lung
Chen, Hong-Sen
Wang, Andrew H.-J.
Yang, An-Suei
High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title_full High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title_fullStr High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title_full_unstemmed High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title_short High throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
title_sort high throughput discovery of influenza virus neutralizing antibodies from phage-displayed synthetic antibody libraries
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663709/
https://www.ncbi.nlm.nih.gov/pubmed/29089574
http://dx.doi.org/10.1038/s41598-017-14823-w
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