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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
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.
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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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