EXCEED THE SPACE PROVIDED. Mechanisms that control initiation of the adaptive immune responses is one of the fundamental questions of immunology. Innate immune recognition plays a critical role in the activation of immune responses. In particular, recognition of infection by a family of Toll-like receptors (TLRs) is a crucial step in the induction of T cell activation. TLRs induce maturation of dendritic cells. Induction of expression of co-stimulatory molecules on dendritic cells is a critical step in naive T cell activation. Activation of T cells is also controlled by suppressor T cells, including CD4+CD25+ regulatory T cells (Tregs). Tregs prevent activation of autoreactive T cells and thus prevent the development of a variety of autoimmune diseases. However, Tregs should not interfere with immune responses directed at pathogens. Because pathogens are recognized by the TLR family, we hypothesize that TLR-mediated recognition should lead to a blockade of Treg-mediated suppression to allow protective immune responses to infecting pathogens. Our preliminary studies provide strong evidence that this is indeed the case. The goal of this proposal is to address multiple aspects of this hypothesis. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI055502-03
Application #
6833461
Study Section
Experimental Immunology Study Section (EI)
Program Officer
Winter, David B
Project Start
2003-07-01
Project End
2007-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
3
Fiscal Year
2005
Total Cost
$367,875
Indirect Cost
Name
Yale University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Okin, Daniel; Medzhitov, Ruslan (2016) The Effect of Sustained Inflammation on Hepatic Mevalonate Pathway Results in Hyperglycemia. Cell 165:343-56
Schenten, Dominik; Nish, Simone A; Yu, Shuang et al. (2014) Signaling through the adaptor molecule MyD88 in CD4+ T cells is required to overcome suppression by regulatory T cells. Immunity 40:78-90
Bezbradica, Jelena S; Rosenstein, Rachel K; DeMarco, Richard A et al. (2014) A role for the ITAM signaling module in specifying cytokine-receptor functions. Nat Immunol 15:333-42
Chang, Pamela V; Hao, Liming; Offermanns, Stefan et al. (2014) The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition. Proc Natl Acad Sci U S A 111:2247-52
Nish, Simone A; Schenten, Dominik; Wunderlich, F Thomas et al. (2014) T cell-intrinsic role of IL-6 signaling in primary and memory responses. Elife 3:e01949
Palm, Noah W; Rosenstein, Rachel K; Yu, Shuang et al. (2013) Bee venom phospholipase A2 induces a primary type 2 response that is dependent on the receptor ST2 and confers protective immunity. Immunity 39:976-85
Gao, Yan; Nish, Simone A; Jiang, Ruoyi et al. (2013) Control of T helper 2 responses by transcription factor IRF4-dependent dendritic cells. Immunity 39:722-32
Jamieson, Amanda M; Pasman, Lesley; Yu, Shuang et al. (2013) Role of tissue protection in lethal respiratory viral-bacterial coinfection. Science 340:1230-4
Palm, Noah W; Medzhitov, Ruslan (2013) Role of the inflammasome in defense against venoms. Proc Natl Acad Sci U S A 110:1809-14
Kotas, Maya E; Jurczak, Michael J; Annicelli, Charles et al. (2013) Role of caspase-1 in regulation of triglyceride metabolism. Proc Natl Acad Sci U S A 110:4810-5

Showing the most recent 10 out of 29 publications