| Grant number: | 17/09491-8 |
| Support Opportunities: | Scholarships in Brazil - Post-Doctoral |
| Start date: | June 01, 2017 |
| End date: | November 30, 2018 |
| Field of knowledge: | Biological Sciences - Immunology - Cellular Immunology |
| Principal Investigator: | Dimas Tadeu Covas |
| Grantee: | Marcelo de Souza Fernandes Pereira |
| Host Institution: | Hemocentro de Ribeirão Preto. Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da USP (HCMRP). Ribeirão Preto , SP, Brazil |
| Associated research grant: | 13/08135-2 - CTC - Center for Cell-Based Therapy, AP.CEPID |
Abstract Most of B-cell neoplasms are responsive to chemotherapy, however, in some patients this treatment shown a non-effective response presenting recurrence. Immunotherapies have been described as an alternative for cancer treatment, been a high innovative technology in which cells of the immune system can be genetically engineered with Chimeric Antigen Receptors (CAR). These cells perform a specific recognition of cancer cells independent of histocompatibility complex.Different types of CARs have been developed to recognize tumor cell specific antigens. Usually, anti-CD19 CAR-modified T cells have been successfully applied in patients with B cell neoplasms, such as Acute Lymphoblastic Leukemia (ALL) and Burkitt's Lymphoma (LB). This approach has shown promising results in clinical trials. Although several groups abroad have demonstrated the efficiency of this treatment in clinical trials, it is important to implant this therapeutic technology in Brazil, and the generation of a murine model of B-cell lymphoid neoplasia as well as, which will be really important to determining The therapeutic potential of CAR-T-CD19 cells in xenogeneic models. (AU) | |
| News published in Agência FAPESP Newsletter about the scholarship: | |
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