Immunogenicity profiling of protein antigens from capsular group B Neisseria meningitidis

Outer membrane vesicle (OMV)- based vaccines have been used to provide strain-specific protection against capsular group B Neisseria meningitidis infections, but the full breadth of the immune response against the components of the OMV has not been established. Sera from adults vaccinated with an OM...

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Veröffentlicht in:Scientific reports 2019-05, Vol.9 (1), p.6843-6843, Article 6843
Hauptverfasser: Awanye, Amaka M., Chang, Chun-Mien, Wheeler, Jun X., Chan, Hannah, Marsay, Leanne, Dold, Christina, Rollier, Christine S., Bird, Louise E., Nettleship, Joanne E., Owens, Raymond J., Pollard, Andrew J., Derrick, Jeremy P.
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Sprache:eng
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Zusammenfassung:Outer membrane vesicle (OMV)- based vaccines have been used to provide strain-specific protection against capsular group B Neisseria meningitidis infections, but the full breadth of the immune response against the components of the OMV has not been established. Sera from adults vaccinated with an OMV vaccine were used to screen 91 outer membrane proteins (OMPs) incorporated in an antigen microarray panel. Antigen-specific IgG levels were quantified pre-vaccination, and after 12 and 18 weeks. These results were compared with IgG levels from mice vaccinated with the same OMV vaccine. The repertoires of highly responding antigens in humans and mice overlapped, but were not identical. The highest responding antigens to human IgG comprised four integral OMPs (PorA, PorB, OpcA and PilQ), a protein which promotes the stability of PorA and PorB (RmpM) and two lipoproteins (BamC and GNA1162). These observations will assist in evaluating the role of minor antigen components within OMVs in providing protection against meningococcal infection. In addition, the relative dominance of responses to integral OMPs in humans emphasizes the importance of this subclass and points to the value of maintaining conformational epitopes from integral membrane proteins in vaccine formulations.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-019-43139-0