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MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis
Abstract Influenza is a major cause of worldwide morbidity and mortality through frequent seasonal epidemics and infrequent pandemics. Morbidity and mortality rates from seasonal influenza are highest in the most frail, such as the elderly, those with underlying chronic conditions and very young ch...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634121/ https://www.ncbi.nlm.nih.gov/pubmed/19453401 http://dx.doi.org/10.1111/j.1750-2659.2008.00059.x |
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author | Banzhoff, Angelika Pellegrini, Michele Del Giudice, Giuseppe Fragapane, Elena Groth, Nicola Podda, Audino |
author_facet | Banzhoff, Angelika Pellegrini, Michele Del Giudice, Giuseppe Fragapane, Elena Groth, Nicola Podda, Audino |
author_sort | Banzhoff, Angelika |
collection | PubMed |
description | Abstract Influenza is a major cause of worldwide morbidity and mortality through frequent seasonal epidemics and infrequent pandemics. Morbidity and mortality rates from seasonal influenza are highest in the most frail, such as the elderly, those with underlying chronic conditions and very young children. Antigenic mismatch between strains recommended for vaccine formulation and circulating viruses can further reduce vaccine efficacy in these populations. Seasonal influenza vaccines with enhanced, cross‐reactive immunogenicity are needed to address these problems and can confer a better immune protection, particularly in seasons were antigenic mismatch occurs. A related issue for vaccine development is the growing threat of pandemic influenza caused by H5N1 avian strains. Vaccines against strains with pandemic potential offer the best approach for reducing the potential impact of a pandemic. However, current non‐adjuvanted pre‐pandemic vaccines offer suboptimal immunogenicity against H5N1. For both seasonal and pre‐pandemic vaccines, the addition of adjuvants may be the best approach for providing enhanced cross‐reactive immunogenicity. MF59(®), the first oil‐in‐water emulsion licensed as an adjuvant for human use, can enhance vaccine immune responses through multiple mechanisms. A trivalent MF59‐adjuvanted seasonal influenza vaccine (Fluad(®)) has shown to induce significantly higher immune responses to influenza vaccination in the elderly, compared with non‐adjuvanted vaccines, and to provide cross‐reactive immunity against divergent influenza strains. Similar results have been generated with a MF59‐adjuvanted H5N1 pre‐pandemic vaccine, which showed higher and broader immunogenicity compared with non‐adjuvanted pre‐pandemic vaccines. |
format | Online Article Text |
id | pubmed-4634121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46341212015-11-27 MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis Banzhoff, Angelika Pellegrini, Michele Del Giudice, Giuseppe Fragapane, Elena Groth, Nicola Podda, Audino Influenza Other Respir Viruses Reviews Abstract Influenza is a major cause of worldwide morbidity and mortality through frequent seasonal epidemics and infrequent pandemics. Morbidity and mortality rates from seasonal influenza are highest in the most frail, such as the elderly, those with underlying chronic conditions and very young children. Antigenic mismatch between strains recommended for vaccine formulation and circulating viruses can further reduce vaccine efficacy in these populations. Seasonal influenza vaccines with enhanced, cross‐reactive immunogenicity are needed to address these problems and can confer a better immune protection, particularly in seasons were antigenic mismatch occurs. A related issue for vaccine development is the growing threat of pandemic influenza caused by H5N1 avian strains. Vaccines against strains with pandemic potential offer the best approach for reducing the potential impact of a pandemic. However, current non‐adjuvanted pre‐pandemic vaccines offer suboptimal immunogenicity against H5N1. For both seasonal and pre‐pandemic vaccines, the addition of adjuvants may be the best approach for providing enhanced cross‐reactive immunogenicity. MF59(®), the first oil‐in‐water emulsion licensed as an adjuvant for human use, can enhance vaccine immune responses through multiple mechanisms. A trivalent MF59‐adjuvanted seasonal influenza vaccine (Fluad(®)) has shown to induce significantly higher immune responses to influenza vaccination in the elderly, compared with non‐adjuvanted vaccines, and to provide cross‐reactive immunity against divergent influenza strains. Similar results have been generated with a MF59‐adjuvanted H5N1 pre‐pandemic vaccine, which showed higher and broader immunogenicity compared with non‐adjuvanted pre‐pandemic vaccines. Blackwell Publishing Ltd 2008-12-09 2008-11 /pmc/articles/PMC4634121/ /pubmed/19453401 http://dx.doi.org/10.1111/j.1750-2659.2008.00059.x Text en © 2008 The Authors. Journal Compilation © 2008 Blackwell Publishing Ltd |
spellingShingle | Reviews Banzhoff, Angelika Pellegrini, Michele Del Giudice, Giuseppe Fragapane, Elena Groth, Nicola Podda, Audino MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title | MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title_full | MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title_fullStr | MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title_full_unstemmed | MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title_short | MF59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
title_sort | mf59(®)‐adjuvanted vaccines for seasonal and pandemic influenza prophylaxis |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634121/ https://www.ncbi.nlm.nih.gov/pubmed/19453401 http://dx.doi.org/10.1111/j.1750-2659.2008.00059.x |
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