Recombinant Immuno-Fragments for C. difficile detection

Information

  • Research Project
  • 6791133
  • ApplicationId
    6791133
  • Core Project Number
    R43AI060271
  • Full Project Number
    1R43AI060271-01
  • Serial Number
    60271
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/2004 - 19 years ago
  • Project End Date
    5/29/2005 - 19 years ago
  • Program Officer Name
    VAN DE VERG, LILLIAN L.
  • Budget Start Date
    9/30/2004 - 19 years ago
  • Budget End Date
    5/29/2005 - 19 years ago
  • Fiscal Year
    2004
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/23/2004 - 20 years ago

Recombinant Immuno-Fragments for C. difficile detection

DESCRIPTION (provided by applicant): The overall goal of this proposed Phase I project is to determine scientific merit and feasibility of constructing highly specific recombinant single chain variable fragment (scFv) antibodies to Clostridium difficile toxin A and toxin B, and detect their presence for rapid, inexpensive, and sensitive diagnosis of Clostridium difficile associated diarrhea (CDAD). We propose to develop recombinant C. difficile anti-toxin A and anti-toxin B scFv and determine their utility as vital tools for the next generation of CDAD diagnostic products. Specific aims are to: (1) evaluate recombinant C. difficile anti-toxin B scFv for ability to detect toxin B, (2) develop a panel of recombinant C. difficile anti-toxin A scFv using an anti-toxin A monoclonal antibody as starting material, using mutagenesis and phage display to improve scFv affinity, (3) evaluate recombinant C. difficile anti-toxin A scFv for ability to detect toxin A, and (4) develop platform technology that demonstrates binding of anti-toxin A and anti-toxin B scFv for use in clinical laboratories for diagnosis of CDAD. ScFv will be evaluated in lateral flow assay and ELISA formats (as both detection and capture antibodies), and fluorescence polarization platforms. Successful completion of the Aims will allow detecting toxin A and toxin B in clinical laboratories for detection of CDAD. Our long term goal is to develop (Phase II study) and market (Phase III commercialization) a superior test for CDAD that meets or exceeds the sensitivities and specificities of currently available tests, is incomparable because it features rapid turn around time and minimizes human and economic loss.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R43
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    100000
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
    NIAID:100000\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    MERIDIAN BIOSCIENCE, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CINCINNATI
  • Organization State
    OH
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    45244
  • Organization District
    UNITED STATES