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The role of T Cell Activation in Type 1 Diabetes. T cell differentiation versus T Cell tolerance

Objetivo

The proposal presented here represents a continuation of the work I have done in the USA on peripheral tolerance and autoimmune diabetes. My goal is to gain a better understanding of the disregulation of the mechanisms of immune tolerance leading to the activation of autoreactive T cells in autoimmune processes.

This will allow us to rationally design new therapeutic strategies against type 1 diabetes in particular, that can prevent or stop the progression of the disease before insulin function is lost. These forms of therapy are inexistent at the present time. The interplay among three types of cells plays an important role in the onset of type 1 diabetes. These are CD8+ T cells, CD4+ T helper cells and antigen-presenting cells (APCs).

In a normal situation, tolerogenic APCs will pick and transport self-antigens from the parenchyma to the draining lymph nodes, where they will silence CD8+ and CD4+ T cells. If CD4+ T cell tolerance fails, CD4+ helper cells will activate APCs, that in turn will promote the differentiation of potentially autoreactive CD8+ T cells into diabetogenic killer cells.

Based on this hypothesis, the aim of this project is to decipher the cellular and molecular interactions responsible for the establishment of T cell tolerance to pancreatic antigens, and the activation of potentially autoreactive T cells leading to autoimmunity.

Ámbito científico (EuroSciVoc)

Palabras clave

Tema(s)

Convocatoria de propuestas

FP6-2002-MOBILITY-5
Consulte otros proyectos de esta convocatoria

Régimen de financiación

EIF - Marie Curie actions-Intra-European Fellowships

Coordinador

CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
Aportación de la UE
Sin datos
Dirección
Rue Michel Ange 3
PARIS
Francia
Coste total
Sin datos