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Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus
Drug combinations are synergistic when their combined efficacy exceeds the sum of the individual actions, but they rarely include ineffective drugs that become effective only in combination. We identified several “enabling pairs” of neutralizing and non-neutralizing anti-ebolavirus monoclonal antibo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s).
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082427/ https://www.ncbi.nlm.nih.gov/pubmed/28402862 http://dx.doi.org/10.1016/j.celrep.2017.03.049 |
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author | Howell, Katie A. Brannan, Jennifer M. Bryan, Christopher McNeal, Andrew Davidson, Edgar Turner, Hannah L. Vu, Hong Shulenin, Sergey He, Shihua Kuehne, Ana Herbert, Andrew S. Qiu, Xiangguo Doranz, Benjamin J. Holtsberg, Frederick W. Ward, Andrew B. Dye, John M. Aman, M. Javad |
author_facet | Howell, Katie A. Brannan, Jennifer M. Bryan, Christopher McNeal, Andrew Davidson, Edgar Turner, Hannah L. Vu, Hong Shulenin, Sergey He, Shihua Kuehne, Ana Herbert, Andrew S. Qiu, Xiangguo Doranz, Benjamin J. Holtsberg, Frederick W. Ward, Andrew B. Dye, John M. Aman, M. Javad |
author_sort | Howell, Katie A. |
collection | PubMed |
description | Drug combinations are synergistic when their combined efficacy exceeds the sum of the individual actions, but they rarely include ineffective drugs that become effective only in combination. We identified several “enabling pairs” of neutralizing and non-neutralizing anti-ebolavirus monoclonal antibodies, whose combination exhibited new functional profiles, including transforming a non-neutralizing antibody to a neutralizer. Sub-neutralizing concentrations of antibodies 2G4 or m8C4 enabled non-neutralizing antibody FVM09 (IC(50) >1 μM) to exhibit potent neutralization (IC(50) 1–10 nM). While FVM09 or m8C4 alone failed to protect Ebola-virus-infected mice, a combination of the two antibodies provided 100% protection. Furthermore, non-neutralizers FVM09 and FVM02 exponentially enhanced the potency of two neutralizing antibodies against both Ebola and Sudan viruses. We identified a hotspot for the binding of these enabling antibody pairs near the interface of the glycan cap and GP2. Enabling cooperativity may be an underappreciated phenomenon for viruses, with implications for the design and development of immunotherapeutics and vaccines. |
format | Online Article Text |
id | pubmed-6082427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Author(s). |
record_format | MEDLINE/PubMed |
spelling | pubmed-60824272018-08-08 Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus Howell, Katie A. Brannan, Jennifer M. Bryan, Christopher McNeal, Andrew Davidson, Edgar Turner, Hannah L. Vu, Hong Shulenin, Sergey He, Shihua Kuehne, Ana Herbert, Andrew S. Qiu, Xiangguo Doranz, Benjamin J. Holtsberg, Frederick W. Ward, Andrew B. Dye, John M. Aman, M. Javad Cell Rep Article Drug combinations are synergistic when their combined efficacy exceeds the sum of the individual actions, but they rarely include ineffective drugs that become effective only in combination. We identified several “enabling pairs” of neutralizing and non-neutralizing anti-ebolavirus monoclonal antibodies, whose combination exhibited new functional profiles, including transforming a non-neutralizing antibody to a neutralizer. Sub-neutralizing concentrations of antibodies 2G4 or m8C4 enabled non-neutralizing antibody FVM09 (IC(50) >1 μM) to exhibit potent neutralization (IC(50) 1–10 nM). While FVM09 or m8C4 alone failed to protect Ebola-virus-infected mice, a combination of the two antibodies provided 100% protection. Furthermore, non-neutralizers FVM09 and FVM02 exponentially enhanced the potency of two neutralizing antibodies against both Ebola and Sudan viruses. We identified a hotspot for the binding of these enabling antibody pairs near the interface of the glycan cap and GP2. Enabling cooperativity may be an underappreciated phenomenon for viruses, with implications for the design and development of immunotherapeutics and vaccines. The Author(s). 2017-04-11 2017-04-11 /pmc/articles/PMC6082427/ /pubmed/28402862 http://dx.doi.org/10.1016/j.celrep.2017.03.049 Text en © 2017 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Howell, Katie A. Brannan, Jennifer M. Bryan, Christopher McNeal, Andrew Davidson, Edgar Turner, Hannah L. Vu, Hong Shulenin, Sergey He, Shihua Kuehne, Ana Herbert, Andrew S. Qiu, Xiangguo Doranz, Benjamin J. Holtsberg, Frederick W. Ward, Andrew B. Dye, John M. Aman, M. Javad Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title | Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title_full | Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title_fullStr | Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title_full_unstemmed | Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title_short | Cooperativity Enables Non-neutralizing Antibodies to Neutralize Ebolavirus |
title_sort | cooperativity enables non-neutralizing antibodies to neutralize ebolavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082427/ https://www.ncbi.nlm.nih.gov/pubmed/28402862 http://dx.doi.org/10.1016/j.celrep.2017.03.049 |
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