Evaluation of the Bacterial Transferrin Receptor as a Vaccine Antigen

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atmire.migration.oldid5155
dc.contributor.advisorSchryvers, Anthony
dc.contributor.authorFegan, Jamie
dc.contributor.committeememberArmstrong, Glen
dc.contributor.committeememberVan Marle, Guido
dc.date.accessioned2016-12-16T19:15:40Z
dc.date.available2016-12-16T19:15:40Z
dc.date.issued2016
dc.date.submitted2016en
dc.description.abstractThe bacterial transferrin receptor has been considered a candidate vaccine antigen for multiple important pathogens, including Neisseria meningitidis. It was previously shown that both components, transferrin binding proteins A (TbpA) and B (TbpB) are required for bacterial survival within the host and both can elicit bactericidal antibodies after immunization. Here, cross reactivity of multiple TbpB variants has been evaluated in a high-throughput ELISA-based assay that was developed to ensure all regions of TbpB are accessible during evaluation. An engineered C-lobe scaffold of TbpB has been used to host surface-exposed regions of TbpA. Antibodies developed against the hybrid antigens were able to bind TbpA on whole bacteria and inhibit TbpA- dependent transferrin-based growth. Serum bactericidal activity was elicited by antisera to these ‘hybrid’ antigens both with and without TbpB present in the targeted strain, indicating individual TbpA loops induce complement-based killing. In N. meningitidis, asymptomatic carriage of the nasopharyngeal mucosa represents the only reservoir of disease. Conjugate capsular vaccines have been shown to reduce the burden of colonization of N. meningitidis, indicating that systemic immunization is able to effect mucosal carriage. The recent development of transgenic mice expressing human CEACAM1, a molecule necessary for bacterial adhesion, has led to the first mucosal colonization model of N. meningitidis. This model has been utilized to evaluate mucosal protection by TbpB and another prominent meningococcal vaccine antigen, factor H binding protein (FHbp). These data suggest that while TbpB is able to elicit protection from both invasive disease and mucosal colonization, FHbp is unable to prevent mucosal colonization while still eliciting systemic protection. TbpB was evaluated as a carrier antigen for the development of conjugate capsular vaccines to target a pathogen by both the polysaccharide capsule and a required protein antigen. TbpB from N. meningitidis was conjugated to the Haemophilus influenzae type B polysaccharide and resultant sera was bactericidal against both N. meningitidis and H. influenzae with no significant decrease in TbpB cross reactivity or meningococcal protection when compared to sera against native TbpB. These data provide a more comprehensive evaluation of the efficacy of transferrin receptor-based vaccines.en_US
dc.identifier.citationFegan, J. (2016). Evaluation of the Bacterial Transferrin Receptor as a Vaccine Antigen (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/25992en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/25992
dc.identifier.urihttp://hdl.handle.net/11023/3488
dc.language.isoeng
dc.publisher.facultyGraduate Studies
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.subjectMicrobiology
dc.subject.classificationVaccinesen_US
dc.subject.classificationProtein Antigensen_US
dc.subject.classificationInfectious Diseasesen_US
dc.subject.classificationNeisseria meningitidisen_US
dc.subject.classificationTransferrin binding proteinsen_US
dc.titleEvaluation of the Bacterial Transferrin Receptor as a Vaccine Antigen
dc.typedoctoral thesis
thesis.degree.disciplineMicrobiology & Infectious Diseases
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameDoctor of Philosophy (PhD)
ucalgary.item.requestcopytrue
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