FAST LIGAND FOR PROTECTION OF TRANSPLANTED B ISLET CELLS

Information

  • Research Project
  • 2536604
  • ApplicationId
    2536604
  • Core Project Number
    R41DK053585
  • Full Project Number
    1R41DK053585-01
  • Serial Number
    53585
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/1/1998 - 26 years ago
  • Project End Date
    9/30/1999 - 25 years ago
  • Program Officer Name
    HARMON, JOAN T.
  • Budget Start Date
    4/1/1998 - 26 years ago
  • Budget End Date
    9/30/1999 - 25 years ago
  • Fiscal Year
    1998
  • Support Year
    1
  • Suffix
  • Award Notice Date
    3/14/1998 - 26 years ago
Organizations

FAST LIGAND FOR PROTECTION OF TRANSPLANTED B ISLET CELLS

DESCRIPTION: (Adapted from the Applicant's Abstract): The goal of the research proposed in this application is the bioengineering of allogeneic and xenogeneic beta islet cells that would be accepted for implantation without encapsulation in a manufactured biomaterial. Recent studies indicate that expression of Fas ligand (FasL) can induce tolerance by stimulation of apoptosis in Fas+ macrophages and activated T cells. Specific Aims of the Phase I research are as follows: (1) Determine if there is increased survival of islets from lpr mice in gld mice compared to gld into lpr mice. (2) Determine if beta islet cells from rat insulin promoter-FasL transgenic mice exhibit prolonged graft survival. (3) Determined if prolonged allograft survival will occur with grafts of mouse and human islets infected with FasL adenovirus. These studies are expected to provide the basis for Phase II work to develop transgenic pigs with human FasL under the control of the insulin promoter for beta islet cell transplantation. The commercial application would be the readily available supply of islet cells with stable Fas L expression for transplantation as an artificial pancreas in patients with diabetes mellitus. PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R41
  • Administering IC
    DK
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    847
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG2
  • Study Section Name
  • Organization Name
    MANDALMED, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    SAN FRANCISCO
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    941071953
  • Organization District
    UNITED STATES