NKT cells are unique T lymphocytes that are known to exert potent immunomodulatory effects, although the mechanisms by which they influence immune responses are not well understood. Unlike most other types of T cells, NKT cells can be functionally activated by self antigens presented by CD1d molecules. This type of autoreactive stimulation is likely to be one of the primary ways that NKT cells are activated in vivo. However, the self antigens recognized by human NKT cells remain poorly characterized, and there is little understanding of the functional consequences of NKT cell autoreactive activation. Based on our preliminary data, we hypothesize that lipid messengers, such as lyso-phospholipids, are auto-antigens for NKT cells, and that this provides a pathway by which NKT cell activation in vivo is directly connected to broader processes of immune regulation. Additionally, we have recently shown that NKT cells induce peripheral blood monocytes to differentiate into immature DCs, and our current data suggests the resulting DCs have distinctive regulatory functions. Hence, we hypothesize that NKT cells influence down-stream immune responses by regulating the differentiation and functional properties of myeloid DCs. Here, we propose: i) to Identify auto-antigens recognized by human NKT cells, and to analyze the molecular requirements for CD1d auto-antigen presentation; ii) to Investigate regulation of NKT cell autoreactivity by physiological lipidmessengers; and iii) to examine the properties of myeloid DC that differentiate in response to NKT cell signals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI074940-01A1
Application #
7682777
Study Section
Innate Immunity and Inflammation Study Section (III)
Program Officer
Miller, Lara R
Project Start
2008-09-12
Project End
2009-04-14
Budget Start
2008-09-12
Budget End
2009-04-14
Support Year
1
Fiscal Year
2008
Total Cost
$330,245
Indirect Cost
Name
University of Wisconsin Madison
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
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Fox, Lisa; Hegde, Subramanya; Gumperz, Jenny E (2010) Natural killer T cells: innate lymphocytes positioned as a bridge between acute and chronic inflammation? Microbes Infect 12:1125-33
Hegde, Subramanya; Fox, Lisa; Wang, Xiaohua et al. (2010) Autoreactive natural killer T cells: promoting immune protection and immune tolerance through varied interactions with myeloid antigen-presenting cells. Immunology 130:471-83
Fox, Lisa M; Cox, Daryl G; Lockridge, Jennifer L et al. (2009) Recognition of lyso-phospholipids by human natural killer T lymphocytes. PLoS Biol 7:e1000228
Hegde, Subramanya; Jankowska-Gan, Ewa; Roenneburg, Drew A et al. (2009) Human NKT cells promote monocyte differentiation into suppressive myeloid antigen-presenting cells. J Leukoc Biol 86:757-68