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Treatment of cattle with DNA-encoded Flt3L and GM-CSF prior to immunization with Theileria parva candidate vaccine antigens induces CD4 and CD8 T cell IFN-γ responses but not CTL responses.

TitleTreatment of cattle with DNA-encoded Flt3L and GM-CSF prior to immunization with Theileria parva candidate vaccine antigens induces CD4 and CD8 T cell IFN-γ responses but not CTL responses.
Publication TypeJournal Article
Year of Publication2011
AuthorsMwangi, DM, Honda, Y, Graham, SP, Pelle, R, Taracha, ELN, Gachanja, J, Nyanjui, JK, Bray, J, Palmer, GH, Brown, WC, Mwangi, W
JournalVet Immunol Immunopathol
Volume140
Issue3-4
Pagination244-51
Date Published2011 Apr 15
ISSN1873-2534
KeywordsAdjuvants, Immunologic, Animals, Antigens, Protozoan, Cattle, CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, Granulocyte-Macrophage Colony-Stimulating Factor, Interferon-gamma, Lymphocyte Activation, Membrane Proteins, Protozoan Vaccines, Recombinant Proteins, T-Lymphocytes, Cytotoxic, Theileria parva, Theileriasis, Vaccines, DNA
Abstract

Theileria parva antigens recognized by cytotoxic T lymphocytes (CTLs) are prime vaccine candidates against East Coast fever in cattle. A strategy for enhancing induction of parasite-specific T cell responses by increasing recruitment and activation of dendritic cells (DCs) at the immunization site by administration of bovine Flt3L and GM-CSF prior to inoculation with DNA vaccine constructs and MVA boost was evaluated. Analysis of immune responses showed induction of significant T. parva-specific proliferation, and IFN-γ-secreting CD4(+) and CD8(+) T cell responses in immunized cattle. However, antigen-specific CTLs were not detected. Following lethal challenge, 5/12 immunized cattle survived by day 21, whereas all the negative controls had to be euthanized due to severe disease, indicating a protective effect of the vaccine (p<0.05). The study demonstrated the potential of this technology to elicit significant MHC class II and class I restricted IFN-γ-secreting CD4(+) and CD8(+) T cells to defined vaccine candidate antigens in a natural host, but also underscores the need to improve strategies for eliciting protective CTL responses.

DOI10.1016/j.vetimm.2010.12.013
Alternate JournalVet. Immunol. Immunopathol.
PubMed ID21288576