| Grant number: | 17/21401-4 |
| Support Opportunities: | Scholarships abroad - Research Internship - Doctorate |
| Start date: | November 01, 2017 |
| End date: | September 01, 2018 |
| Field of knowledge: | Biological Sciences - Immunology - Applied Immunology |
| Principal Investigator: | Beatriz Rossetti Ferreira |
| Grantee: | Andressa Fisch |
| Supervisor: | Timothy Connelley |
| Host Institution: | Escola de Enfermagem de Ribeirão Preto (EERP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
| Institution abroad: | University of Edinburgh, Scotland |
| Associated to the scholarship: | 14/11010-0 - Development of a recombinant multicomponent chimeric vaccine based in proteins epitopes from Rhipicephalus microplus ticks, BP.DR |
Abstract Ticks are important vectors of diseases to humans and animals and promote significant losses in cattle production sector. The vaccines currently available against ticks show variable outcome of protection between the cattle and little lasting memory immune response, indicating the need to develop more efficient vaccines. The development of epitope-based vaccines rather than full antigen vaccines has some advantages. Among them: possibility of inclusion of several antigens in a single construct, selection of epitopes shared between different tick species, improved security, reduced cost and ease of manufacturing. In order to identify T cell epitopes for epitope-based vaccine construction, we propose to characterize the BoLA DRB3 (bovine MHC II) haplotypes from bovines of our previous experiments through NGS; subsequently, we will stimulate the bovine PBMC with the antigens used in vaccinations and identify the eluted peptides from BoLA DRB3 through mass spectrometry. The sequences of peptides and DRB3 haplotypes will be analyzed by Machine learning in order to predict the interactions between these molecules. Hereafter, the sequences of the identified epitopes will be used for the synthesis of a multi epitope-based protein, together with the sequences identified by phage display and peptide-array (ongoing work), allowing expression of the fused epitopes in a single structure. The epitope-based recombinant protein will be used to immunize host that subsequently will undergo a challenge infestation with R. sanguineus and R. microplus ticks in which the efficacy of the vaccine will be evaluated. (AU) | |
| News published in Agência FAPESP Newsletter about the scholarship: | |
| More itemsLess items | |
| TITULO | |
| Articles published in other media outlets ( ): | |
| More itemsLess items | |
| VEICULO: TITULO (DATA) | |
| VEICULO: TITULO (DATA) | |