Biomedical Sciences ETDs
Publication Date
Summer 7-29-2025
Abstract
Bacteriophage virus-like particles are highly immunogenic, self-assembling platforms used for various vaccines. This work shows efforts to explore new vaccine candidates against Chlamydia trachomatis, targeting proteins that play critical roles in attachment and entry into the host cell, as well as in pathogenesis and bacteria proliferation. This work also shows the optimization of previously identified candidates, by investigating how altering routes of immunization can change the antibody profiles elicited, both systemically and locally. Finally, this work shows the establishment of various Chlamydia infection models in an effort to expand the ways in which vaccine efficacy can be investigated, particularly in penis, anorectal, and sexual transmission models of infection. Overall, this work furthers efforts to establish a multi-epitope Chlamydia vaccine that is able to protect against infection at various anatomic sites, and is optimized for protection.
Document Type
Dissertation
Language
English
Degree Name
Biomedical Sciences
Level of Degree
Doctoral
Department Name
Biomedical Sciences Graduate Program
First Committee Member (Chair)
Bryce Chackerian, PhD
Second Committee Member
Kathryn Frietze, PhD
Third Committee Member
Judy Cannon, PhD
Fourth Committee Member
Terry Wu, PhD
Fifth Committee Member
Russell Morton, PhD
Recommended Citation
Jamus, Andzoa N.. "EXPLORATION, EXPANSION, AND OPTIMIZATION OF BACTERIOPHAGE VIRUS-LIKE PARTICLE VACCINES." (2025). https://digitalrepository.unm.edu/biom_etds/285