Immunoproteomic Profiling of Bordetella pertussis Outer Membrane Vesicle Vaccine Reveals Broad and Balanced Humoral Immunogenicity | Zendy

René H. M. Raeven | Zendy; Larissa van der Maas | Zendy; Wichard Tilstra | Zendy; Joost P. Uittenbogaard | Zendy; Tim H. E. Bindels | Zendy; Betsy Kuipers | Zendy; Arno van der Ark | Zendy; Jeroen L. A. Pennings | Zendy; Elly van Riet | Zendy; Wim Jiskoot | Zendy; Gideon Kersten | Zendy; Bernard Metz | Zendy

Open Access

Immunoproteomic Profiling of Bordetella pertussis Outer Membrane Vesicle Vaccine Reveals Broad and Balanced Humoral Immunogenicity

Author(s) -

René H. M. Raeven,

Larissa van der Maas,

Wichard Tilstra,

Joost P. Uittenbogaard,

Tim H. E. Bindels,

Betsy Kuipers,

Arno van der Ark,

Jeroen L. A. Pennings,

Elly van Riet,

Wim Jiskoot,

Gideon Kersten,

Bernard Metz

Publication year - 2015

Publication title -

journal of proteome research

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.644

H-Index - 161

eISSN - 1535-3907

pISSN - 1535-3893

DOI - 10.1021/acs.jproteome.5b00258

Subject(s) - immunogenicity , bordetella pertussis , antigen , humoral immunity , antibody , pertactin , biology , virology , whooping cough , proteome , immunology , microbiology and biotechnology , vaccination , pertussis toxin , g protein , bacteria , biochemistry , genetics , receptor

The current resurgence of whooping cough is alarming, and improved pertussis vaccines are thought to offer a solution. Outer membrane vesicle vaccines (omvPV) are potential vaccine candidates, but omvPV-induced humoral responses have not yet been characterized in detail. The purpose of this study was to determine the antigen composition of omvPV and to elucidate the immunogenicity of the individual antigens. Quantitative proteome analysis revealed the complex composition of omvPV. The omvPV immunogenicity profile in mice was compared to those of classic whole cell vaccine (wPV), acellular vaccine (aPV), and pertussis infection. Pertussis-specific antibody levels, antibody isotypes, IgG subclasses, and antigen specificity were determined after vaccination or infection by using a combination of multiplex immunoassays, two-dimensional immunoblotting, and mass spectrometry. The vaccines and infection raised strong antibody responses, but large quantitative and qualitative differences were measured. The highest antibody levels were obtained by omvPV. All IgG subclasses (IgG1/IgG2a/IgG2b/IgG3) were elicited by omvPV and in a lower magnitude by wPV, but not by aPV (IgG1) or infection (IgG2a/b). The majority of omvPV-induced antibodies were directed against Vag8, BrkA, and LPS. The broad and balanced humoral response makes omvPV a promising pertussis vaccine candidate.

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