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Learning from prepandemic data to forecast viral escape

Effective pandemic preparedness relies on anticipating viral mutations that are able to evade host immune responses to facilitate vaccine and therapeutic design. However, current strategies for viral evolution prediction are not available early in a pandemic—experimental approaches require host poly...

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Autores principales: Thadani, Nicole N., Gurev, Sarah, Notin, Pascal, Youssef, Noor, Rollins, Nathan J., Ritter, Daniel, Sander, Chris, Gal, Yarin, Marks, Debora S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599991/
https://www.ncbi.nlm.nih.gov/pubmed/37821700
http://dx.doi.org/10.1038/s41586-023-06617-0
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author Thadani, Nicole N.
Gurev, Sarah
Notin, Pascal
Youssef, Noor
Rollins, Nathan J.
Ritter, Daniel
Sander, Chris
Gal, Yarin
Marks, Debora S.
author_facet Thadani, Nicole N.
Gurev, Sarah
Notin, Pascal
Youssef, Noor
Rollins, Nathan J.
Ritter, Daniel
Sander, Chris
Gal, Yarin
Marks, Debora S.
author_sort Thadani, Nicole N.
collection PubMed
description Effective pandemic preparedness relies on anticipating viral mutations that are able to evade host immune responses to facilitate vaccine and therapeutic design. However, current strategies for viral evolution prediction are not available early in a pandemic—experimental approaches require host polyclonal antibodies to test against(1–16), and existing computational methods draw heavily from current strain prevalence to make reliable predictions of variants of concern(17–19). To address this, we developed EVEscape, a generalizable modular framework that combines fitness predictions from a deep learning model of historical sequences with biophysical and structural information. EVEscape quantifies the viral escape potential of mutations at scale and has the advantage of being applicable before surveillance sequencing, experimental scans or three-dimensional structures of antibody complexes are available. We demonstrate that EVEscape, trained on sequences available before 2020, is as accurate as high-throughput experimental scans at anticipating pandemic variation for SARS-CoV-2 and is generalizable to other viruses including influenza, HIV and understudied viruses with pandemic potential such as Lassa and Nipah. We provide continually revised escape scores for all current strains of SARS-CoV-2 and predict probable further mutations to forecast emerging strains as a tool for continuing vaccine development (evescape.org).
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spelling pubmed-105999912023-10-27 Learning from prepandemic data to forecast viral escape Thadani, Nicole N. Gurev, Sarah Notin, Pascal Youssef, Noor Rollins, Nathan J. Ritter, Daniel Sander, Chris Gal, Yarin Marks, Debora S. Nature Article Effective pandemic preparedness relies on anticipating viral mutations that are able to evade host immune responses to facilitate vaccine and therapeutic design. However, current strategies for viral evolution prediction are not available early in a pandemic—experimental approaches require host polyclonal antibodies to test against(1–16), and existing computational methods draw heavily from current strain prevalence to make reliable predictions of variants of concern(17–19). To address this, we developed EVEscape, a generalizable modular framework that combines fitness predictions from a deep learning model of historical sequences with biophysical and structural information. EVEscape quantifies the viral escape potential of mutations at scale and has the advantage of being applicable before surveillance sequencing, experimental scans or three-dimensional structures of antibody complexes are available. We demonstrate that EVEscape, trained on sequences available before 2020, is as accurate as high-throughput experimental scans at anticipating pandemic variation for SARS-CoV-2 and is generalizable to other viruses including influenza, HIV and understudied viruses with pandemic potential such as Lassa and Nipah. We provide continually revised escape scores for all current strains of SARS-CoV-2 and predict probable further mutations to forecast emerging strains as a tool for continuing vaccine development (evescape.org). Nature Publishing Group UK 2023-10-11 2023 /pmc/articles/PMC10599991/ /pubmed/37821700 http://dx.doi.org/10.1038/s41586-023-06617-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Thadani, Nicole N.
Gurev, Sarah
Notin, Pascal
Youssef, Noor
Rollins, Nathan J.
Ritter, Daniel
Sander, Chris
Gal, Yarin
Marks, Debora S.
Learning from prepandemic data to forecast viral escape
title Learning from prepandemic data to forecast viral escape
title_full Learning from prepandemic data to forecast viral escape
title_fullStr Learning from prepandemic data to forecast viral escape
title_full_unstemmed Learning from prepandemic data to forecast viral escape
title_short Learning from prepandemic data to forecast viral escape
title_sort learning from prepandemic data to forecast viral escape
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599991/
https://www.ncbi.nlm.nih.gov/pubmed/37821700
http://dx.doi.org/10.1038/s41586-023-06617-0
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