Additive and Synergistic Bactericidal Activity of Antibodies Directed against Minor Outer Membrane Proteins of Neisseria meningitidis

Author:

Weynants Vincent E.1,Feron Christiane M.1,Goraj Karine K.1,Bos Martine P.2,Denoël Philippe A.1,Verlant Vincent G.1,Tommassen Jan2,Peak Ian R. A.3,Judd Ralph C.4,Jennings Michael P.5,Poolman Jan T.1

Affiliation:

1. GlaxoSmithKline Biologicals, B-1330 Rixensart, Belgium

2. Department of Molecular Microbiology, Utrecht University, 3584-CH Utrecht, The Netherlands

3. Institute for Glycomics, Griffith University, Southport QLD 4215, Australia

4. Division of Biological Sciences, University of Montana, Missoula, Montana 59812

5. School of Molecular & Microbial Sciences, University of Queensland, Brisbane QLD 4072, Australia

Abstract

ABSTRACT Neisseria meningitidis serogroup B is a major cause of bacterial meningitis in younger populations. The available vaccines are based on outer membrane vesicles obtained from wild-type strains. In children less than 2 years old they confer protection only against strains expressing homologous PorA, a major, variable outer membrane protein (OMP). We genetically modified a strain in order to eliminate PorA and to overproduce one or several minor and conserved OMPs. Using a mouse model mimicking children's PorA-specific bactericidal activity, it was demonstrated that overproduction of more than one minor OMP is required to elicit antibodies able to induce complement-mediated killing of strains expressing heterologous PorA. It is concluded that a critical density of bactericidal antibodies needs to be reached at the surface of meningococci to induce complement-mediated killing. With minor OMPs, this threshold is reached when more than one antigen is targeted, and this allows cross-protection.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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