A single dose polyanhydride-based vaccine platform promotes and maintains anti-GnRH antibody titers

dc.contributor.author Schaut, Robert
dc.contributor.author Jackman, John
dc.contributor.author Brewer, Matt
dc.contributor.author Hostetter, Jesse
dc.contributor.author Mendoza, Kriscelle
dc.contributor.author Vela-Ramirez, Julia
dc.contributor.author Kelly, Sean
dc.contributor.author Dell’Anna, Giuseppe
dc.contributor.author Howard, Joan
dc.contributor.author Narasimhan, Balaji
dc.contributor.author Zhou, Wen
dc.contributor.author Jones, Douglas
dc.contributor.department Veterinary Pathology
dc.contributor.department Veterinary Clinical Sciences
dc.contributor.department Department of Chemical and Biological Engineering
dc.contributor.department Department of Industrial and Manufacturing Systems Engineering
dc.contributor.department Nanovaccine Institute
dc.date 2018-11-03T06:27:01.000
dc.date.accessioned 2020-07-07T05:15:41Z
dc.date.available 2020-07-07T05:15:41Z
dc.date.issued 2018-02-08
dc.description.abstract <p>Traditionally, vaccination strategies require an initial priming vaccination followed by an antigen boost to generate adequate immunity. Here we describe vaccination against a self-peptide for reproductive sterilization utilizing a three-stage vaccine platform consisting of gonadotropin releasing hormone multiple antigenic peptide (GnRH-MAP) as a soluble injection coupled with subcutaneous administration of polyanhydride-immobilized GnRH-MAP and a cyto-exclusive implant containing GnRH-MAP dendrimer-loaded polyanhydride. This strategy generated and maintained cell-mediated and humoral immunity for up to 41 weeks after a single vaccination in mice with enhanced antibody avidity over time. All intact implants had a grossly visible tissue interface with neovascularization and lymphocytic aggregates. Despite detectable immunity, sterility was not achieved and the immune response did not lead to azoospermia in male mice nor prevent estrus and ovulation in female mice. However, the vaccine delivery device is tunable and the immunogen, adjuvants and release rates can all be modified to enhance immunity. This technology has broad implications for the development of long-term vaccination schemes.</p>
dc.description.comments <p>This article is published as Schaut, Robert G., Matthew T. Brewer, Jesse M. Hostetter, Kriscelle Mendoza, Julia E. Vela-Ramirez, Sean M. Kelly, John K. Jackman, Giuseppe Dell’Anna, Joan M. Howard, Balaji Narasimhan, Wen Zhou, and Douglas E. Jones. "A single dose polyanhydride-based vaccine platform promotes and maintains anti-GnRH antibody titers." <em>Vaccine</em> 36, no. 7 (2018): 1016-1023. DOI: <a href="https://dx.doi.org/10.1016/j.vaccine.2017.12.050" target="_blank">10.1016/j.vaccine.2017.12.050</a>.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/vpath_pubs/103/
dc.identifier.articleid 1107
dc.identifier.contextkey 13228328
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath vpath_pubs/103
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/92427
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/vpath_pubs/103/2018_Brewer_SingleDose.pdf|||Fri Jan 14 18:18:20 UTC 2022
dc.source.uri 10.1016/j.vaccine.2017.12.050
dc.subject.disciplines Biochemical and Biomolecular Engineering
dc.subject.disciplines Operational Research
dc.subject.disciplines Veterinary Pathology and Pathobiology
dc.subject.disciplines Veterinary Preventive Medicine, Epidemiology, and Public Health
dc.subject.disciplines Veterinary Toxicology and Pharmacology
dc.subject.keywords GnRH
dc.subject.keywords Vaccine
dc.subject.keywords Immunocastration
dc.subject.keywords Antibodies
dc.subject.keywords Implant
dc.subject.keywords Single-dose
dc.title A single dose polyanhydride-based vaccine platform promotes and maintains anti-GnRH antibody titers
dc.type article
dc.type.genre article
dspace.entity.type Publication
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