The broad objective of this project are to study the stimuli that induce tolerance in normal T cells and in vivo, with emphasis on the roles of costimulators, antigen-presenting cells and cytokines, and to examine the tolerance sensitivity of different T cell populations, including cells that escape negative selection in the thymus. A major emphasis is on the use of T cell receptor (TCR) transgenic mice.
The specific aims of the project are the following. 1. Tolerance in naive CD4+ T cells in vitro The development of tolerance will be studied in normal CD4+ T cells isolated from transgenic mice expressing a TCR specific for cytochrome c + I-Ek. The types of APCs that induce tolerance, and their costimulators, will be examined. The ability of cytokines to prevent tolerance will be studied. The functional impairment and fate of tolerant cells will be examined. 2. Mechanisms of tolerance induction in vivo Peripheral T cell tolerance will be induced in normal and TCR transgenic mice by high-dose aqueous antigen, antigen targeted to B cells, and oral antigen administration. The influence of cytokines on T cell tolerance will be examined with specific antagonists. The role of B cells as tolerogenic APCs will be studied in B-deficient mice. Thus, the is project addresses fundamental questions about the induction and maintenance of peripheral T cell tolerance in normal T cells and in vivo, and the physiologic significance of peripheral tolerance.

Project Start
1999-07-01
Project End
1999-09-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Proekt, Irina; Miller, Corey N; Lionakis, Michail S et al. (2017) Insights into immune tolerance from AIRE deficiency. Curr Opin Immunol 49:71-78
Sanchez Rodriguez, Robert; Pauli, Mariela L; Neuhaus, Isaac M et al. (2014) Memory regulatory T cells reside in human skin. J Clin Invest 124:1027-36
Villalta, S Armando; Rosenthal, Wendy; Martinez, Leonel et al. (2014) Regulatory T cells suppress muscle inflammation and injury in muscular dystrophy. Sci Transl Med 6:258ra142
Stumpf, Melanie; Zhou, Xuyu; Chikuma, Shunsuke et al. (2014) Tyrosine 201 of the cytoplasmic tail of CTLA-4 critically affects T regulatory cell suppressive function. Eur J Immunol 44:1737-46
Baumjohann, Dirk; Kageyama, Robin; Clingan, Jonathan M et al. (2013) The microRNA cluster miR-17?92 promotes TFH cell differentiation and represses subset-inappropriate gene expression. Nat Immunol 14:840-8
Stumpf, Melanie; Zhou, Xuyu; Bluestone, Jeffrey A (2013) The B7-independent isoform of CTLA-4 functions to regulate autoimmune diabetes. J Immunol 190:961-9
Gardner, James M; Metzger, Todd C; McMahon, Eileen J et al. (2013) Extrathymic Aire-expressing cells are a distinct bone marrow-derived population that induce functional inactivation of CD4? T cells. Immunity 39:560-72
Martínez-Llordella, Marc; Esensten, Jonathan H; Bailey-Bucktrout, Samantha L et al. (2013) CD28-inducible transcription factor DEC1 is required for efficient autoreactive CD4+ T cell response. J Exp Med 210:1603-19
Jeker, Lukas T; Zhou, Xuyu; Blelloch, Robert et al. (2013) DGCR8-mediated production of canonical microRNAs is critical for regulatory T cell function and stability. PLoS One 8:e66282
Bailey-Bucktrout, Samantha L; Martinez-Llordella, Marc; Zhou, Xuyu et al. (2013) Self-antigen-driven activation induces instability of regulatory T cells during an inflammatory autoimmune response. Immunity 39:949-62

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