| Grant number: | 16/02840-4 |
| Support Opportunities: | Scholarships in Brazil - Doctorate (Direct) |
| Start date: | March 01, 2018 |
| End date: | July 31, 2019 |
| Field of knowledge: | Biological Sciences - Immunology - Cellular Immunology |
| Principal Investigator: | Jose Ronnie Carvalho de Vasconcelos |
| Grantee: | Barbara Ferri Moraschi |
| Host Institution: | Centro de Terapia Celular e Molecular. Universidade Federal de São Paulo (UNIFESP). Campus São Paulo. São Paulo , SP, Brazil |
Abstract Heterologous prime-boost vaccination using plasmid DNA followed by replication defective human recombinant adenovirus type 5 - both expressing the amastigote surface protein 2 (ASP-2) of Trypanosoma cruzi- is a powerful strategy to elicit CD8+ T cells, mainly CD8+ T effector memory cells (TEM), that mediated protective immunity against the parasite protozoan Trypanosoma cruzi. Specific TEM cells with CD44High, CD11aHigh, CD62LLow, KLRG1High e CD127High phenotype are polyfunctional, because secrete IFN-g and TNF-a, mediate cytotoxicity, can remain for a long time and are resistant to immune erosion. Despite the high frequency of specific TEM CD8+ cells induced by this type of vaccination, seek new strategies that can further increase the frequencies of specific T cells and especially the with TCM phenotype (CD44High, CD11aHigh, CD62LHigh and CD127High). A possible strategy in this regard is the use of pharmacological mTOR (rapamycin target protein in mammals) inhibitor, called rapamycin. Treatment with this drug, which is commercially available and approved for human use, were able to increase the frequency of TCM CD8+ in some experimental models of viral infections. Based on these data, the aim of this project will test whether treatment with rapamycin can increase the frequency of specific memory CD8 T cells induced by heterologous "prime-boost" vaccination. If this works, this strategy can be used to improve the efficiency of this and other vaccinations. | |
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