| Grant number: | 07/53940-0 |
| Support Opportunities: | Research Projects - Thematic Grants |
| Start date: | October 01, 2007 |
| End date: | September 30, 2012 |
| Field of knowledge: | Biological Sciences - Immunology - Cellular Immunology |
| Principal Investigator: | João Santana da Silva |
| Grantee: | João Santana da Silva |
| Host Institution: | Faculdade de Medicina de Ribeirão Preto (FMRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
| City of the host institution: | Ribeirão Preto |
| Principal investigators | Marcos Antonio Rossi |
| Principal investigators | Júlio César Voltarelli |
| Associated scholarship(s): | 09/13890-9 - Evaluation of the role of T regulator and Th17 cells during experimental infection with Toxoplasma gondii,
BP.PD 08/09851-5 - The effect of statins as immune modulators during experimental Trypanosoma cruzi infection, BP.PD |
Abstract
This project is based on two distinct goals. One is to study the role of regulatory T cells and Th17 lymphocytes on the control of immune response. The T cells orquestrate the defense against invaders, but they can also lead to uncontrolled immune-mediated diseases. The classical Th1/Th2 axis until now has explained immunity against invaders as well as its control in order to avoid immune-mediated diseases. However, other recently described lymphocytes are involved in control or in delivery of immunity, such as, respectively, natural regulatory T (Treg) cells, and inflammatory Th17 lymphocytes. This project will study the role of Tregs and ThI7 cells in immune responses against Trypanosoma cruzi, Paracoccidiodes brasiliensis and Leishmania braziliensis, as well as their role in bacterial periodontal disease and in breast and skin (non-melanoma) cancers and tumors or with the other side of immune responses, that is, lack of control leading to autoimmunity and tissue damage. We will determine the roles of ThI7 in tissue damage and of Treg in persistence of tumors and pathogens, as well as some of the mechanisms whereby these phenomena occur, opening new possibilities for immune interventions. The other aim is to strengthen our research group. The diversity of diseases examined in this proposal and the multidisciplinary nature of its technical and scientific approaches result in the congregation of a large group of scientists, which already interact regularly. The project works with a strong graduate program. Support from F APESP will improve the group's working conditions, therefore strengthening it and increasing the amount and quality of scientific knowledge it generates, as well as the number and quality of scientists prepared by the graduate program. (AU)
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