Literature DB >> 15755595

The concept of "tailor-made", protein-based, outer membrane vesicle vaccines against meningococcal disease.

Johan Holst1, Berit Feiring, Lisbeth M Naess, Gunnstein Norheim, Paul Kristiansen, E Arne Høiby, Klaus Bryn, Philipp Oster, Paolo Costantino, Muhamed-Kheir Taha, Jean-Michel Alonso, Dominique A Caugant, Elisabeth Wedege, Ingeborg S Aaberge, Rino Rappuoli, Einar Rosenqvist.   

Abstract

Protein-based, outer membrane vesicle (OMV) vaccines have previously proven to be efficacious against serogroup B meningococcal disease in Norway and Cuba. Currently, a public health intervention is going on in order to control a serogroup B epidemic in New Zealand. The scale-up and standardization of vaccine production required for controlling the New Zealand epidemic has allowed the establishment of large-scale GMP manufacturing for OMV vaccines. The outcome of this will be licensing of the vaccine in New Zealand and possibly other countries. The availability of licensed OMV vaccines raises the question of whether such vaccines may provide the opportunity to control other outbreaks and epidemics. For instance, such a vaccine could control a localised outbreak of group B meningococci in Normandy, France. "Tailor-made" vaccines, focusing on the sub-capsular antigens may also be considered for use in sub-Saharan Africa for the prevention of the recurrent outbreaks by serogroups A and W135 meningococci. This assumption is based on the epidemiological observation that meningococcal outbreaks in Africa are clonal and are strikingly stable regarding their phenotypic characteristics.

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Year:  2005        PMID: 15755595     DOI: 10.1016/j.vaccine.2005.01.058

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  27 in total

1.  Functional and specific antibody responses in adult volunteers in new zealand who were given one of two different meningococcal serogroup B outer membrane vesicle vaccines.

Authors:  E Wedege; K Bolstad; A Aase; T K Herstad; L McCallum; E Rosenqvist; P Oster; D Martin
Journal:  Clin Vaccine Immunol       Date:  2007-05-09

Review 2.  Biology and pathogenesis of the evolutionarily successful, obligate human bacterium Neisseria meningitidis.

Authors:  David S Stephens
Journal:  Vaccine       Date:  2009-05-23       Impact factor: 3.641

3.  Expression of factor H binding protein of meningococcus responds to oxygen limitation through a dedicated FNR-regulated promoter.

Authors:  Francesca Oriente; Vincenzo Scarlato; Isabel Delany
Journal:  J Bacteriol       Date:  2009-11-30       Impact factor: 3.490

4.  A critical threshold of meningococcal factor H binding protein expression is required for increased breadth of protective antibodies elicited by native outer membrane vesicle vaccines.

Authors:  Oliver Koeberling; Isabel Delany; Dan M Granoff
Journal:  Clin Vaccine Immunol       Date:  2011-03-02

Review 5.  Review of meningococcal group B vaccines.

Authors:  Dan M Granoff
Journal:  Clin Infect Dis       Date:  2010-03-01       Impact factor: 9.079

6.  Immunization with live Neisseria lactamica protects mice against meningococcal challenge and can elicit serum bactericidal antibodies.

Authors:  Yanwen Li; Qian Zhang; Megan Winterbotham; Eva Mowe; Andrew Gorringe; Christoph M Tang
Journal:  Infect Immun       Date:  2006-09-11       Impact factor: 3.441

7.  Immunogenicity, reactogenicity, and safety of a P1.7b,4 strain-specific serogroup B meningococcal vaccine given to preteens.

Authors:  Jamie Hosking; Kumanan Rasanathan; Florina Chan Mow; Catherine Jackson; Diana Martin; Jane O'Hallahan; Philipp Oster; Ellen Ypma; Stewart Reid; Ingeborg Aaberge; Sue Crengle; Joanna Stewart; Diana Lennon
Journal:  Clin Vaccine Immunol       Date:  2007-09-26

8.  Immunity to Neisseria meningitidis group B in adults despite lack of serum bactericidal antibody.

Authors:  Jo Anne Welsch; Dan Granoff
Journal:  Clin Vaccine Immunol       Date:  2007-10-03

9.  Detection of outer membrane vesicles in Synechocystis PCC 6803.

Authors:  Yehudah A Pardo; Catalina Florez; Kristopher M Baker; Jeffrey W Schertzer; Gretchen J Mahler
Journal:  FEMS Microbiol Lett       Date:  2015-09-10       Impact factor: 2.742

10.  Meningococcal outer membrane vesicle vaccines derived from mutant strains engineered to express factor H binding proteins from antigenic variant groups 1 and 2.

Authors:  Oliver Koeberling; Serena Giuntini; Anja Seubert; Dan M Granoff
Journal:  Clin Vaccine Immunol       Date:  2008-12-24
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