Servicio de Información Comunitario sobre Investigación y Desarrollo - CORDIS

FP6

AIP IN AUTOIMMUNITY Informe resumido

Project ID: 40998
Financiado con arreglo a: FP6-MOBILITY
País: France

Final Activity Report Summary - AIP IN AUTOIMMUNITY (AIP (Aire-Interacting Protein) regulates autoantigen expression)

Dysfunction of the immune system, due to breakdown of self-tolerance, is the cause of development of autoimmune diseases, and has serious, disabling and even fatal consequences. An increase of the mechanisms of immune tolerance to exogenous would also be beneficial in the context of organ transplantation, allergy and gene therapy. Thus, the knowledge of immunological mechanisms involved in tolerance represents a major challenge to improve both the understanding and treatment of autoimmune diseases but also those processes.

The main objective of this project was to better understand the mechanisms of action of Aire gene in the central and peripheral tolerance. This work allowed us a better understanding of the involvement of the interaction of two types of cells (Aire expressing epithelial cells and dendritic cells) in deletion process of autoreactive T cells. We also showed that Aire expression is restricted to the thymus and not expressed in dendritic cells. In addition, Aire-deficient mouse only present a mild autoimmune phenotype and does not entirely mimic the human form of the disease. Interestingly, we found that Aire-deficient mice have more aggressive CD8 T cells than the normal mice.

Although the mouse model has enabled substantial progress in this area, it seemed useful to develop a new animal model for which the physiopathology might be closer to those observed in mice. Thus, we are currently working on a new animal model in Aire-deficiency: in rats. We analysed the interactions between thymic epithelial cells that express Aire and thymic dendritic cells, two cell populations playing a major role in T cell tolerance. Indeed, we found that rat dendritic cell subsets were able to specifically kill thymic epithelial cells expressing Aire. Interestingly this killing activity was never found in mouse which supports the use of a rat model. We will also use this model to study the involvement of Aire in alloreactivity.

Contacto

Régis JOSIEN, (Chargé de Recherche INSERM)
Tel.: 33 2 4087410
Fax: 33 2 4087411
Correo electrónico
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