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Proof of principle for epitope-focused vaccine design
Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Multiple major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260937/ https://www.ncbi.nlm.nih.gov/pubmed/24499818 http://dx.doi.org/10.1038/nature12966 |
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author | Correia, Bruno E. Bates, John T. Loomis, Rebecca J. Baneyx, Gretchen Carrico, Christopher Jardine, Joseph G. Rupert, Peter Correnti, Colin Kalyuzhniy, Oleksandr Vittal, Vinayak Connell, Mary J. Stevens, Eric Schroeter, Alexandria Chen, Man MacPherson, Skye Serra, Andreia M. Adachi, Yumiko Holmes, Margaret A. Li, Yuxing Klevit, Rachel E. Graham, Barney S. Wyatt, Richard T. Baker, David Strong, Roland K. Crowe, James E. Johnson, Philip R. Schief, William R. |
author_facet | Correia, Bruno E. Bates, John T. Loomis, Rebecca J. Baneyx, Gretchen Carrico, Christopher Jardine, Joseph G. Rupert, Peter Correnti, Colin Kalyuzhniy, Oleksandr Vittal, Vinayak Connell, Mary J. Stevens, Eric Schroeter, Alexandria Chen, Man MacPherson, Skye Serra, Andreia M. Adachi, Yumiko Holmes, Margaret A. Li, Yuxing Klevit, Rachel E. Graham, Barney S. Wyatt, Richard T. Baker, David Strong, Roland K. Crowe, James E. Johnson, Philip R. Schief, William R. |
author_sort | Correia, Bruno E. |
collection | PubMed |
description | Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Multiple major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases. Hence, new vaccine design methods to induce epitope-specific neutralizing antibodies are needed. Here we show, with a neutralization epitope from respiratory syncytial virus (RSV), that computational protein design can generate small, thermally and conformationally stable protein scaffolds that accurately mimic the viral epitope structure and induce potent neutralizing antibodies. These scaffolds represent promising leads for research and development of a human RSV vaccine needed to protect infants, young children and the elderly. More generally, the results provide proof of principle for epitope-focused and scaffold-based vaccine design, and encourage the evaluation and further development of these strategies for a variety of other vaccine targets including antigenically highly variable pathogens such as HIV and influenza. |
format | Online Article Text |
id | pubmed-4260937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42609372014-12-09 Proof of principle for epitope-focused vaccine design Correia, Bruno E. Bates, John T. Loomis, Rebecca J. Baneyx, Gretchen Carrico, Christopher Jardine, Joseph G. Rupert, Peter Correnti, Colin Kalyuzhniy, Oleksandr Vittal, Vinayak Connell, Mary J. Stevens, Eric Schroeter, Alexandria Chen, Man MacPherson, Skye Serra, Andreia M. Adachi, Yumiko Holmes, Margaret A. Li, Yuxing Klevit, Rachel E. Graham, Barney S. Wyatt, Richard T. Baker, David Strong, Roland K. Crowe, James E. Johnson, Philip R. Schief, William R. Nature Article Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Multiple major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases. Hence, new vaccine design methods to induce epitope-specific neutralizing antibodies are needed. Here we show, with a neutralization epitope from respiratory syncytial virus (RSV), that computational protein design can generate small, thermally and conformationally stable protein scaffolds that accurately mimic the viral epitope structure and induce potent neutralizing antibodies. These scaffolds represent promising leads for research and development of a human RSV vaccine needed to protect infants, young children and the elderly. More generally, the results provide proof of principle for epitope-focused and scaffold-based vaccine design, and encourage the evaluation and further development of these strategies for a variety of other vaccine targets including antigenically highly variable pathogens such as HIV and influenza. 2014-02-05 2014-03-13 /pmc/articles/PMC4260937/ /pubmed/24499818 http://dx.doi.org/10.1038/nature12966 Text en http://creativecommons.org/licenses/by-nc/3.0/ Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Correia, Bruno E. Bates, John T. Loomis, Rebecca J. Baneyx, Gretchen Carrico, Christopher Jardine, Joseph G. Rupert, Peter Correnti, Colin Kalyuzhniy, Oleksandr Vittal, Vinayak Connell, Mary J. Stevens, Eric Schroeter, Alexandria Chen, Man MacPherson, Skye Serra, Andreia M. Adachi, Yumiko Holmes, Margaret A. Li, Yuxing Klevit, Rachel E. Graham, Barney S. Wyatt, Richard T. Baker, David Strong, Roland K. Crowe, James E. Johnson, Philip R. Schief, William R. Proof of principle for epitope-focused vaccine design |
title | Proof of principle for epitope-focused vaccine design |
title_full | Proof of principle for epitope-focused vaccine design |
title_fullStr | Proof of principle for epitope-focused vaccine design |
title_full_unstemmed | Proof of principle for epitope-focused vaccine design |
title_short | Proof of principle for epitope-focused vaccine design |
title_sort | proof of principle for epitope-focused vaccine design |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260937/ https://www.ncbi.nlm.nih.gov/pubmed/24499818 http://dx.doi.org/10.1038/nature12966 |
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