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A naturally protective epitope of limited variability as an influenza vaccine target

Current antigenic targets for influenza vaccine development are either highly immunogenic epitopes of high variability or conserved epitopes of low immunogenicity. This requires continuous update of the variable epitopes in the vaccine formulation or boosting of immunity to invariant epitopes of low...

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Autores principales: Thompson, Craig P., Lourenço, José, Walters, Adam A., Obolski, Uri, Edmans, Matthew, Palmer, Duncan S., Kooblall, Kreepa, Carnell, George W., O’Connor, Daniel, Bowden, Thomas A., Pybus, Oliver G., Pollard, Andrew J., Temperton, Nigel J., Lambe, Teresa, Gilbert, Sarah C., Gupta, Sunetra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155085/
https://www.ncbi.nlm.nih.gov/pubmed/30242149
http://dx.doi.org/10.1038/s41467-018-06228-8
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author Thompson, Craig P.
Lourenço, José
Walters, Adam A.
Obolski, Uri
Edmans, Matthew
Palmer, Duncan S.
Kooblall, Kreepa
Carnell, George W.
O’Connor, Daniel
Bowden, Thomas A.
Pybus, Oliver G.
Pollard, Andrew J.
Temperton, Nigel J.
Lambe, Teresa
Gilbert, Sarah C.
Gupta, Sunetra
author_facet Thompson, Craig P.
Lourenço, José
Walters, Adam A.
Obolski, Uri
Edmans, Matthew
Palmer, Duncan S.
Kooblall, Kreepa
Carnell, George W.
O’Connor, Daniel
Bowden, Thomas A.
Pybus, Oliver G.
Pollard, Andrew J.
Temperton, Nigel J.
Lambe, Teresa
Gilbert, Sarah C.
Gupta, Sunetra
author_sort Thompson, Craig P.
collection PubMed
description Current antigenic targets for influenza vaccine development are either highly immunogenic epitopes of high variability or conserved epitopes of low immunogenicity. This requires continuous update of the variable epitopes in the vaccine formulation or boosting of immunity to invariant epitopes of low natural efficacy. Here we identify a highly immunogenic epitope of limited variability in the head domain of the H1 haemagglutinin protein. We show that a cohort of young children exhibit natural immunity to a set of historical influenza strains which they could not have previously encountered and that this is partially mediated through the epitope. Furthermore, vaccinating mice with these epitope conformations can induce immunity to human H1N1 influenza strains that have circulated since 1918. The identification of epitopes of limited variability offers a mechanism by which a universal influenza vaccine can be created; these vaccines would also have the potential to protect against newly emerging influenza strains.
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spelling pubmed-61550852018-09-28 A naturally protective epitope of limited variability as an influenza vaccine target Thompson, Craig P. Lourenço, José Walters, Adam A. Obolski, Uri Edmans, Matthew Palmer, Duncan S. Kooblall, Kreepa Carnell, George W. O’Connor, Daniel Bowden, Thomas A. Pybus, Oliver G. Pollard, Andrew J. Temperton, Nigel J. Lambe, Teresa Gilbert, Sarah C. Gupta, Sunetra Nat Commun Article Current antigenic targets for influenza vaccine development are either highly immunogenic epitopes of high variability or conserved epitopes of low immunogenicity. This requires continuous update of the variable epitopes in the vaccine formulation or boosting of immunity to invariant epitopes of low natural efficacy. Here we identify a highly immunogenic epitope of limited variability in the head domain of the H1 haemagglutinin protein. We show that a cohort of young children exhibit natural immunity to a set of historical influenza strains which they could not have previously encountered and that this is partially mediated through the epitope. Furthermore, vaccinating mice with these epitope conformations can induce immunity to human H1N1 influenza strains that have circulated since 1918. The identification of epitopes of limited variability offers a mechanism by which a universal influenza vaccine can be created; these vaccines would also have the potential to protect against newly emerging influenza strains. Nature Publishing Group UK 2018-09-21 /pmc/articles/PMC6155085/ /pubmed/30242149 http://dx.doi.org/10.1038/s41467-018-06228-8 Text en © The Author(s) 2018 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
Thompson, Craig P.
Lourenço, José
Walters, Adam A.
Obolski, Uri
Edmans, Matthew
Palmer, Duncan S.
Kooblall, Kreepa
Carnell, George W.
O’Connor, Daniel
Bowden, Thomas A.
Pybus, Oliver G.
Pollard, Andrew J.
Temperton, Nigel J.
Lambe, Teresa
Gilbert, Sarah C.
Gupta, Sunetra
A naturally protective epitope of limited variability as an influenza vaccine target
title A naturally protective epitope of limited variability as an influenza vaccine target
title_full A naturally protective epitope of limited variability as an influenza vaccine target
title_fullStr A naturally protective epitope of limited variability as an influenza vaccine target
title_full_unstemmed A naturally protective epitope of limited variability as an influenza vaccine target
title_short A naturally protective epitope of limited variability as an influenza vaccine target
title_sort naturally protective epitope of limited variability as an influenza vaccine target
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155085/
https://www.ncbi.nlm.nih.gov/pubmed/30242149
http://dx.doi.org/10.1038/s41467-018-06228-8
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