Sexually transmitted infections (STIs) are causing a hidden epidemic. Everyday infected individuals and their families quietly suffer physically, psychologically and financially. Worldwide, STIs are a major economic burden with direct medical costs for treating these diseases in United States alone is $15.3 billion per year. As with many diseases and infections, prevention is the key and with our current technology the best hope for prevention is microbicides. The work set forth in this thesis examined three vastly different microbicides each with very different modes for preventing the initial stages of HIV-1 infection. The prototypic SDS Hydrogel is a broad-spectrum microbicide. We show that our prototypic SDS Hydrogel has potent antiviral activity against enveloped (HIV-1 and HSV-2) and non-enveloped (HPV-11) sexually transmitted viruses. The second microbicide is comprised of a liposomal delivered short interfering RNA (siRNA) pool targeting human chemokine receptor 5 (CCR5). The down-regulation of CCR5 along with other molecules (gp340, syndecans, a4[beta]7 integrin), which allow HIV-1 to remain infectious, may potentially inhibit binding of R5 forms of HIV-1 from binding to the co-receptor, therefore, preventing the subsequent infection. Lastly, the recombinant L. plantarum secreting cyanovirin is a pro-biotic microbicide that decreased HIV-1 infectivity in vitro and we were able to recolonize human vaginal epithelia ex vivo and in vivo.
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Title
Microbicidal approaches to interdict virus infections in human epithelial cell cultures, organ tissue cultures and human epithelial xenografts
Creators
Veronica M. Holmes - DU
Contributors
Mary K. Howett (Advisor) - Drexel University (1970-)
Awarding Institution
Drexel University
Degree Awarded
Doctor of Philosophy (Ph.D.)
Publisher
Drexel University; Philadelphia, Pennsylvania
Resource Type
Dissertation
Language
English
Academic Unit
Bioscience and Biotechnology [Historical]; College of Arts and Sciences; Drexel University
Other Identifier
3473; 991014632318504721
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