The study of class I genes/proteins up until recently has focused on class Ia (classical) molecules and their role in presentation of peptide antigens to CD8 T cells. However, there is now great interest in the study of nonclassical class I molecules which play many important and unique roles in the immune response to infectious agents. In this grant we will characterize and dissect the function of several nonclassical class I molecules. Based on the expertise of our group, we will focus on the following class I molecules/genes; viz. Qa-1, mFcRn. Several approaches will be used to delineate their function which include the analysis of the immune response in mice selectively lacking class Ia molecules, the expression of class I molecules (classical and nonclassical) in hepatocytes of normal and immunostimulated animals, the role of the mFcRn is controlling the level of ligands which bind this receptor, and a characterization of newly discovered genes in the M region. This project will lead to an understanding of 1) the role that nonclassical class I molecules play in the response to bacterial and viral infection, 2) the expression of class I molecules in the liver in normal and diseased states together with the factors that control their expression, 3) a molecular, structural and functional characterization of M region molecules, 4) and how the mFcRn can be used to increase the therapeutic efficiency of cytokines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI037818-07
Application #
6373468
Study Section
Special Emphasis Panel (ZAI1-VSG-M (M1))
Program Officer
Kraemer, Kristy A
Project Start
1995-09-15
Project End
2003-08-31
Budget Start
2001-09-01
Budget End
2002-08-31
Support Year
7
Fiscal Year
2001
Total Cost
$623,647
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Lambracht-Washington, Doris; Moore, Yuki F; Wonigeit, Kurt et al. (2008) Structure and expression of MHC class Ib genes of the central M region in rat and mouse: M4, M5, and M6. Immunogenetics 60:131-45
Chen, Ming; Tabaczewski, Piotr; Truscott, Steven M et al. (2005) Hepatocytes express abundant surface class I MHC and efficiently use transporter associated with antigen processing, tapasin, and low molecular weight polypeptide proteasome subunit components of antigen processing and presentation pathway. J Immunol 175:1047-55
Gunturi, Anasuya; Berg, Rance E; Crossley, Emily et al. (2005) The role of TCR stimulation and TGF-beta in controlling the expression of CD94/NKG2A receptors on CD8 T cells. Eur J Immunol 35:766-75
Gimenez-Barcons, Mireia; Wang, Chunfu; Chen, Ming et al. (2005) The oncogenic potential of hepatitis C virus NS5A sequence variants is associated with PKR regulation. J Interferon Cytokine Res 25:152-64
Hermel, Evan; Hart, Andrew J; Gunduz, Irfan et al. (2004) Polymorphism and conservation of the genes encoding Qa1 molecules. Immunogenetics 56:639-49
Kumanovics, Attila; Fischer Lindahl, Kirsten (2004) Good copy, bad copy: choosing animal models for HLA-linked diseases. Curr Opin Genet Dev 14:258-63
Gunturi, Anasuya; Berg, Rance E; Forman, James (2004) The role of CD94/NKG2 in innate and adaptive immunity. Immunol Res 30:29-34
Moore, Yuki F; Lambracht-Washington, Doris; Tabaczewski, Piotr et al. (2004) Murine MHC class Ib gene, H2-M2, encodes a conserved surface-expressed glycoprotein. Immunogenetics 56:1-11
Lambracht-Washington, Doris; Fischer Lindahl, Kirsten (2004) Active MHC class Ib genes in rat are pseudogenes in the mouse. Immunogenetics 56:118-21
Kurepa, Zoran; Su, Jie; Forman, James (2003) Memory phenotype of CD8+ T cells in MHC class Ia-deficient mice. J Immunol 170:5414-20

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