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dc.contributor.advisorMwangi, Waithaka
dc.creatorMartin, Cameron Lee
dc.date.accessioned2017-08-21T14:43:11Z
dc.date.available2017-08-21T14:43:11Z
dc.date.created2017-05
dc.date.issued2017-05-10
dc.date.submittedMay 2017
dc.identifier.urihttps://hdl.handle.net/1969.1/161578
dc.description.abstractLack of safe and effective adjuvants is a major hindrance to the development of efficacious vaccines. Signaling via CD40 pathway leads to enhanced antigen processing and presentation, nitric oxide expression, pro-inflammatory cytokine expression by antigen presenting cells, and stimulation of B-cells to undergo somatic hypermutation, immunoglobulin class switching, and proliferation. Agonistic anti-CD40 antibodies have shown promising adjuvant qualities in human and mouse vaccine studies. An antiCD40 monoclonal antibody (mAb), designated 2E4E4, was identified and shown to have strong agonistic effects on primary cells from multiple livestock species. The mAb recognize swine, bovine, caprine, and ovine CD40, and evoked 25 fold or greater proliferation of peripheral blood mononuclear cells (PBMCs) from these species relative to cells incubated with an isotype control (p<0.001). In addition, the mAb induced significant nitric oxide (p<0.0001) release by bovine macrophages. Furthermore, the mAb upregulated the expression of MHC-II by PBMCs, and stimulated significant p<0.0001) IL-1α, IL-6, IL- 8, and TNF-α expression by PBMCs. These results suggest that the mAb 2E4E4 can target and stimulate cells from multiple livestock species and thus, it is a potential candidate for adjuvant development. This the first study to report an anti-swine CD40 agonistic mAb that is also broadly reactive against multiple species.en
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.subjectAgonistic anti-CD40 mAben
dc.subjectOvineen
dc.subjectCaprineen
dc.subjectBovineen
dc.subjectVaccinesen
dc.subjectAdjuvanten
dc.titleCharacterization of a Broadly Reactive Anti-CD40 Agonistic Monoclonal Antibody for Potential Use as an Adjuvanten
dc.typeThesisen
thesis.degree.departmentVeterinary Pathobiologyen
thesis.degree.disciplineBiomedical Sciencesen
thesis.degree.grantorTexas A & M Universityen
thesis.degree.nameMaster of Scienceen
thesis.degree.levelMastersen
dc.contributor.committeeMemberWaghela, Suryakant
dc.contributor.committeeMemberCriscitiello, Michael
dc.contributor.committeeMemberWelsh, Jane
dc.contributor.committeeMemberRathore, Keerti
dc.type.materialtexten
dc.date.updated2017-08-21T14:43:11Z
local.etdauthor.orcid0000-0002-7242-8212


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