The absence of the Autoimmune regulator (Aire) protein causes inflammation of multiple organs, in human patients with autoimmune polyglandular syndrome (APS I) and in mice with deficiencies of the aire gene. Inflammation is accompanied by autoantibodies to organ-specific antigens. In aire-/- mice, lymphocytes are required for development of chronic inflammation, and a majority of lymphocytes in inflammatory lesions are B cells. The goal of this study is to test the hypothesis that the activation of self-reactive B lymphocytes makes an important contribution to the autoimmune attack against organ-specific antigens.
The specific aims of this study include: 1) assessing whether B cells are required for the development of organ-specific autoimmune disease, determining the ability of self-reactive immunoglobulin to elicit or accelerate disease, and establishing which effector molecules are essential for the emergence of inflammatory B cells, and 2) identifying a panel of tissue-specific antigens recognized by self-reactive aire-/- B and T cells. Because Aire function is critical to the thymic expression of peripheral organ-specific proteins and to clonal deletion of self-reactive thymocytes, establishing a coincidence between thymically expressed antigens and the specificities of disease-associated lymphocytes will be crucial in understanding how central tolerance prevents organ-specific pathology. Defining the lymphocyte subsets and the effector molecules that operate in the progression of autoimmune disease may suggest novel, directed therapeutic strategies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AI062010-01
Application #
6837775
Study Section
Special Emphasis Panel (ZRG1-F07 (20))
Program Officer
Prograis, Lawrence J
Project Start
2004-07-16
Project End
2006-07-15
Budget Start
2004-07-16
Budget End
2005-07-15
Support Year
1
Fiscal Year
2004
Total Cost
$56,536
Indirect Cost
Name
Joslin Diabetes Center
Department
Type
DUNS #
071723084
City
Boston
State
MA
Country
United States
Zip Code
02215
Gavanescu, Irina; Benoist, Christophe; Mathis, Diane (2008) B cells are required for Aire-deficient mice to develop multi-organ autoinflammation: A therapeutic approach for APECED patients. Proc Natl Acad Sci U S A 105:13009-14
Gray, Daniel H D; Gavanescu, Irina; Benoist, Christophe et al. (2007) Danger-free autoimmune disease in Aire-deficient mice. Proc Natl Acad Sci U S A 104:18193-8
Gavanescu, Irina; Kessler, Benedikt; Ploegh, Hidde et al. (2007) Loss of Aire-dependent thymic expression of a peripheral tissue antigen renders it a target of autoimmunity. Proc Natl Acad Sci U S A 104:4583-7