Our recent studies have indicated a critical role for the T-box transcription factor T-bet in the regulation of class switching in B cells as well as in autoantibody production in systemic autoimmune disease: T-bet deficiency dramatically impairs IFN-gamma-mediated class switching to IgG2a as well as the generation of autoantibodies in the MRL/Ipr murine model of lupus, and conversely enhances IL-4-related responses, such as IgE production. Using genetically mutant mice and in vitro cell culture systems, we propose here to further delineate the role of T-bet in both conventional and autoimmune B cell responses by defining and characterizing the molecular pathways in which this novel pathogenic and therapeutic target regulates isotype switching, cellular proliferation, and the activation of mature, autoreactive B lymphocytes. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI057471-06
Application #
7346917
Study Section
Immunological Sciences Study Section (IMS)
Program Officer
Peyman, John A
Project Start
2004-01-01
Project End
2008-12-31
Budget Start
2008-01-01
Budget End
2008-12-31
Support Year
6
Fiscal Year
2008
Total Cost
$232,541
Indirect Cost
Name
Roche Palo Alto, LLC
Department
Type
DUNS #
063548663
City
Palo Alto
State
CA
Country
United States
Zip Code
94304
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Jonsson, Helena; Allen, Paul; Peng, Stanford L (2005) Inflammatory arthritis requires Foxo3a to prevent Fas ligand-induced neutrophil apoptosis. Nat Med 11:666-71
Jonsson, H; Peng, S L (2005) Forkhead transcription factors in immunology. Cell Mol Life Sci 62:397-409
Srivatsan, Subhashini; Peng, Stanford L (2005) Cutting edge: Foxj1 protects against autoimmunity and inhibits thymocyte egress. J Immunol 175:7805-9

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