The induction of peripheral tolerance is critical for deterrence of autoimmunity. Most self-reactive T cells are deleted during development in the thymus. However, this deletion process is not absolute and occasionally some self-reactive T cells can escape to the periphery. These self-reactive cells must then either be deleted or regulated in the periphery to prevent autoimmunity. To study these processes we generated mice where antigen expression can be tightly controlled in the small intestinal epithelial cells or in CD11c+ cells (dendritic cells) by the administration of doxycycline. Our system provides the unique ability to examine the endogenous T cell response to tissue-specific and developmentally regulated self antigen. First, we will determine the effect of developmentally regulated intestine-specific antigen on endogenous CDS T cells. We intend to turn antigen on for various lengths of time and define the requirements to initiate an autoimmune response or tolerance. We will directly test whether antigen encounter is critical for generation T cell tolerance. We next aim to determine the consequences of memory T cell encounter with developmentally regulated antigen. We intend to generate pathogen-specific memory T cells and then turn on antigen, allowing us to directly test if memory T cells can be tolerized. Together, these aims will allow us to closely examine the consequences of exposing T cells to tissue-specific and developmentally regulated antigen at various stages of activation. Thus, the studies described herein will provide key insights into the mechanisms controlling tolerance versus autoimmunity in the intestinal mucosa.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AI084328-01
Application #
7749715
Study Section
Special Emphasis Panel (ZRG1-F07-E (20))
Program Officer
Prograis, Lawrence J
Project Start
2009-09-01
Project End
2011-08-31
Budget Start
2009-09-01
Budget End
2010-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$47,210
Indirect Cost
Name
University of Connecticut
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030
Bose, Tina O; Pham, Quynh-Mai; Jellison, Evan R et al. (2013) CD11a regulates effector CD8 T cell differentiation and central memory development in response to infection with Listeria monocytogenes. Infect Immun 81:1140-51
Jellison, Evan R; Turner, Michael J; Blair, David A et al. (2012) Distinct mechanisms mediate naive and memory CD8 T-cell tolerance. Proc Natl Acad Sci U S A 109:21438-43
Obar, Joshua J; Jellison, Evan R; Sheridan, Brian S et al. (2011) Pathogen-induced inflammatory environment controls effector and memory CD8+ T cell differentiation. J Immunol 187:4967-78