Cargando…
Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses
While vaccines remain the best tool for preventing influenza virus infections, they have demonstrated low to moderate effectiveness in recent years. Seasonal influenza vaccines typically consist of wild-type influenza A and B viruses that are limited in their ability to elicit protective immune resp...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925519/ https://www.ncbi.nlm.nih.gov/pubmed/33654128 http://dx.doi.org/10.1038/s41598-020-79590-7 |
_version_ | 1783659285612331008 |
---|---|
author | Allen, James D. Ross, Ted M. |
author_facet | Allen, James D. Ross, Ted M. |
author_sort | Allen, James D. |
collection | PubMed |
description | While vaccines remain the best tool for preventing influenza virus infections, they have demonstrated low to moderate effectiveness in recent years. Seasonal influenza vaccines typically consist of wild-type influenza A and B viruses that are limited in their ability to elicit protective immune responses against co-circulating influenza virus variant strains. Improved influenza virus vaccines need to elicit protective immune responses against multiple influenza virus drift variants within each season. Broadly reactive vaccine candidates potentially provide a solution to this problem, but their efficacy may begin to wane as influenza viruses naturally mutate through processes that mediates drift. Thus, it is necessary to develop a method that commercial vaccine manufacturers can use to update broadly reactive vaccine antigens to better protect against future and currently circulating viral variants. Building upon the COBRA technology, nine next-generation H3N2 influenza hemagglutinin (HA) vaccines were designed using a next generation algorithm and design methodology. These next-generation broadly reactive COBRA H3 HA vaccines were superior to wild-type HA vaccines at eliciting antibodies with high HAI activity against a panel of historical and co-circulating H3N2 influenza viruses isolated over the last 15 years, as well as the ability to neutralize future emerging H3N2 isolates. |
format | Online Article Text |
id | pubmed-7925519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79255192021-03-04 Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses Allen, James D. Ross, Ted M. Sci Rep Article While vaccines remain the best tool for preventing influenza virus infections, they have demonstrated low to moderate effectiveness in recent years. Seasonal influenza vaccines typically consist of wild-type influenza A and B viruses that are limited in their ability to elicit protective immune responses against co-circulating influenza virus variant strains. Improved influenza virus vaccines need to elicit protective immune responses against multiple influenza virus drift variants within each season. Broadly reactive vaccine candidates potentially provide a solution to this problem, but their efficacy may begin to wane as influenza viruses naturally mutate through processes that mediates drift. Thus, it is necessary to develop a method that commercial vaccine manufacturers can use to update broadly reactive vaccine antigens to better protect against future and currently circulating viral variants. Building upon the COBRA technology, nine next-generation H3N2 influenza hemagglutinin (HA) vaccines were designed using a next generation algorithm and design methodology. These next-generation broadly reactive COBRA H3 HA vaccines were superior to wild-type HA vaccines at eliciting antibodies with high HAI activity against a panel of historical and co-circulating H3N2 influenza viruses isolated over the last 15 years, as well as the ability to neutralize future emerging H3N2 isolates. Nature Publishing Group UK 2021-03-02 /pmc/articles/PMC7925519/ /pubmed/33654128 http://dx.doi.org/10.1038/s41598-020-79590-7 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Allen, James D. Ross, Ted M. Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title | Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title_full | Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title_fullStr | Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title_full_unstemmed | Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title_short | Next generation methodology for updating HA vaccines against emerging human seasonal influenza A(H3N2) viruses |
title_sort | next generation methodology for updating ha vaccines against emerging human seasonal influenza a(h3n2) viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925519/ https://www.ncbi.nlm.nih.gov/pubmed/33654128 http://dx.doi.org/10.1038/s41598-020-79590-7 |
work_keys_str_mv | AT allenjamesd nextgenerationmethodologyforupdatinghavaccinesagainstemerginghumanseasonalinfluenzaah3n2viruses AT rosstedm nextgenerationmethodologyforupdatinghavaccinesagainstemerginghumanseasonalinfluenzaah3n2viruses |