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Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future
The utility of wild-type outer membrane vesicle (wtOMV) vaccines against serogroup B (MenB) meningococcal disease has been explored since the 1970s. Public health interventions in Cuba, Norway and New Zealand have demonstrated that these protein-based vaccines can prevent MenB disease. Data from lar...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901813/ https://www.ncbi.nlm.nih.gov/pubmed/23857274 http://dx.doi.org/10.4161/hv.24129 |
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author | Holst, Johan Oster, Philipp Arnold, Richard Tatley, Michael V. Næss, Lisbeth M. Aaberge, Ingeborg S. Galloway, Yvonne McNicholas, Anne O’Hallahan, Jane Rosenqvist, Einar Black, Steven |
author_facet | Holst, Johan Oster, Philipp Arnold, Richard Tatley, Michael V. Næss, Lisbeth M. Aaberge, Ingeborg S. Galloway, Yvonne McNicholas, Anne O’Hallahan, Jane Rosenqvist, Einar Black, Steven |
author_sort | Holst, Johan |
collection | PubMed |
description | The utility of wild-type outer membrane vesicle (wtOMV) vaccines against serogroup B (MenB) meningococcal disease has been explored since the 1970s. Public health interventions in Cuba, Norway and New Zealand have demonstrated that these protein-based vaccines can prevent MenB disease. Data from large clinical studies and retrospective statistical analyses in New Zealand give effectiveness estimates of at least 70%. A consistent pattern of moderately reactogenic and safe vaccines has been seen with the use of approximately 60 million doses of three different wtOMV vaccine formulations. The key limitation of conventional wtOMV vaccines is their lack of broad protective activity against the large diversity of MenB strains circulating globally. The public health intervention in New Zealand (between 2004–2008) when MeNZB was used to control a clonal MenB epidemic, provided a number of new insights regarding international and public-private collaboration, vaccine safety surveillance, vaccine effectiveness estimates and communication to the public. The experience with wtOMV vaccines also provide important information for the next generation of MenB vaccines designed to give more comprehensive protection against multiple strains. |
format | Online Article Text |
id | pubmed-3901813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-39018132014-03-10 Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future Holst, Johan Oster, Philipp Arnold, Richard Tatley, Michael V. Næss, Lisbeth M. Aaberge, Ingeborg S. Galloway, Yvonne McNicholas, Anne O’Hallahan, Jane Rosenqvist, Einar Black, Steven Hum Vaccin Immunother Review The utility of wild-type outer membrane vesicle (wtOMV) vaccines against serogroup B (MenB) meningococcal disease has been explored since the 1970s. Public health interventions in Cuba, Norway and New Zealand have demonstrated that these protein-based vaccines can prevent MenB disease. Data from large clinical studies and retrospective statistical analyses in New Zealand give effectiveness estimates of at least 70%. A consistent pattern of moderately reactogenic and safe vaccines has been seen with the use of approximately 60 million doses of three different wtOMV vaccine formulations. The key limitation of conventional wtOMV vaccines is their lack of broad protective activity against the large diversity of MenB strains circulating globally. The public health intervention in New Zealand (between 2004–2008) when MeNZB was used to control a clonal MenB epidemic, provided a number of new insights regarding international and public-private collaboration, vaccine safety surveillance, vaccine effectiveness estimates and communication to the public. The experience with wtOMV vaccines also provide important information for the next generation of MenB vaccines designed to give more comprehensive protection against multiple strains. Landes Bioscience 2013-06-01 2013-03-07 /pmc/articles/PMC3901813/ /pubmed/23857274 http://dx.doi.org/10.4161/hv.24129 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Review Holst, Johan Oster, Philipp Arnold, Richard Tatley, Michael V. Næss, Lisbeth M. Aaberge, Ingeborg S. Galloway, Yvonne McNicholas, Anne O’Hallahan, Jane Rosenqvist, Einar Black, Steven Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title | Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title_full | Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title_fullStr | Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title_full_unstemmed | Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title_short | Vaccines against meningococcal serogroup B disease containing outer membrane vesicles (OMV): Lessons from past programs and implications for the future |
title_sort | vaccines against meningococcal serogroup b disease containing outer membrane vesicles (omv): lessons from past programs and implications for the future |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901813/ https://www.ncbi.nlm.nih.gov/pubmed/23857274 http://dx.doi.org/10.4161/hv.24129 |
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