Show simple item record

Rational Vaccine Design by Reverse & Structural Vaccinology and Ontology

dc.contributor.authorOng, Edison
dc.date.accessioned2021-06-08T23:11:27Z
dc.date.available2021-06-08T23:11:27Z
dc.date.issued2021
dc.date.submitted2021
dc.identifier.urihttps://hdl.handle.net/2027.42/167997
dc.description.abstractVaccination is one of the most successful public health interventions in modern medicine. However, it is still challenging to develop effective vaccines against many infectious diseases such as tuberculosis, HIV, and malaria. There are challenges in integrating the high volume, variety, and variability of vaccine-related data and rationally designing effective and safe vaccines efficiently. In my thesis study, I systematically and comprehensively analyzed manually annotated protective vaccine antigens in the Protegen database and identified these protective antigens' enriched patterns. I then created Vaxign-ML, a novel machine learning-based reverse vaccinology method based on the curated Protegen data for rational vaccine design. Vaxign-ML was used to successfully predict vaccine antigens for tuberculosis and Coronavirus Disease 2019 (COVID-19). I also developed a new structural vaccinology design program that optimizes COVID-19 spike glycoprotein as a vaccine candidate for enhanced vaccine protection via T cell epitope engineering. The vaccine antigens selected and optimized by Reverse and Structural Vaccinology in this dissertation are subjected to future experimental verification. Furthermore, I created a community-based Ontology of Host-Pathogen Interactions (OHPI), which served as a platform to semantically represent the interactions between host and virulence factors that are also protective antigens. I developed the Vaccine Investigation Ontology (VIO) for standardized metadata representation for high throughput vaccine OMICS data analysis. Overall, my thesis research aims to uncover protective antigen patterns, create methods/tools to effectively develop vaccines against infectious diseases of public health significance, and strengthen our understanding of vaccine protection mechanisms. These works can be further expanded and integrated with other technologies such as epitope prediction, molecular epidemiology, and high-throughput sequencing to build the foundation of precision vaccinology.
dc.language.isoen_US
dc.subjectbioinformatics
dc.subjectvaccine design
dc.subjectimmunology
dc.subjectreverse vaccinology
dc.subjectstructural vaccinology
dc.subjectontology
dc.titleRational Vaccine Design by Reverse & Structural Vaccinology and Ontology
dc.typeThesis
dc.description.thesisdegreenamePhDen_US
dc.description.thesisdegreedisciplineBioinformatics
dc.description.thesisdegreegrantorUniversity of Michigan, Horace H. Rackham School of Graduate Studies
dc.contributor.committeememberHe, Yongqun
dc.contributor.committeememberYang, Zhenhua
dc.contributor.committeememberKirschner, Denise E
dc.contributor.committeememberNajarian, Kayvan
dc.subject.hlbsecondlevelMicrobiology and Immunology
dc.subject.hlbtoplevelScience
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/167997/1/edong_1.pdf
dc.identifier.doihttps://dx.doi.org/10.7302/1424
dc.identifier.orcid0000-0002-5159-414X
dc.identifier.name-orcidOng, Edison; 0000-0002-5159-414Xen_US
dc.working.doi10.7302/1424en
dc.owningcollnameDissertations and Theses (Ph.D. and Master's)


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.