NOVEL DRUG DISCOVERY FOR RHEUMATOID ARTHRITIS

Information

  • Research Project
  • 6989817
  • ApplicationId
    6989817
  • Core Project Number
    R43AR050865
  • Full Project Number
    1R43AR050865-01A1
  • Serial Number
    50865
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/13/2005 - 19 years ago
  • Project End Date
    8/31/2007 - 17 years ago
  • Program Officer Name
    GRETZ, ELIZABETH
  • Budget Start Date
    9/13/2005 - 19 years ago
  • Budget End Date
    8/31/2007 - 17 years ago
  • Fiscal Year
    2005
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    9/13/2005 - 19 years ago

NOVEL DRUG DISCOVERY FOR RHEUMATOID ARTHRITIS

[unreadable] DESCRIPTION (provided by applicant): The long-term objective of this project is to develop small molecule inhibitors of MHC class II activity for the treatment of rheumatoid arthritis (RA). The strong genetic association between specific MHC class II alleles, such as HLA-DR molecules containing the shared epitope, and susceptibility to RA provides support to a mechanism in which disease-associated MHC molecules selectively activate CD4 T cells. The hypothesis of this project is that small molecules that block T cell receptor (TCR):HLA-DR-peptide complex formation can prevent autoreactive T cell activation and chronic inflammatory processes in the affect joints. The investigator has developed sensitive screening assays to detect TCR:HLA-DR-peptide interactions and methods to produce sufficient amounts of soluble and functional TCR and HLA-DR-peptide reagents to support analysis of libraries of small molecules. Preliminary studies with another TCR:HLA-peptide pair demonstrate that compounds that specifically inhibit HLA activity in vitro and in vivo can be identified using these screening methods. The specific aims of the project are to further develop high-throughput screening assays to identify and characterize small molecules that inhibit TCR:HLA-DR-peptide interactions, to examine a large and diverse collection of small molecules for inhibitory activity and to test the immunosuppressive effects of these compounds in T cell-based assays. The results from these studies will provide useful information about TCR:HLA-peptide interactions and could form the basis of a novel class of immunosuppressive drugs to treat human T-cell mediated autoimmune diseases. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES
  • Activity
    R43
  • Administering IC
    AR
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    112209
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    846
  • Ed Inst. Type
  • Funding ICs
    NIAMS:112209\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    ALTOR BIOSCIENCE CORPORATION
  • Organization Department
  • Organization DUNS
  • Organization City
    MIRAMAR
  • Organization State
    FL
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    330253958
  • Organization District
    UNITED STATES