Novel Protein Adjuvant

Information

  • Research Project
  • 7267934
  • ApplicationId
    7267934
  • Core Project Number
    R21AI060713
  • Full Project Number
    5R21AI060713-02
  • Serial Number
    60713
  • FOA Number
    PA-04-19
  • Sub Project Id
  • Project Start Date
    7/15/2006 - 18 years ago
  • Project End Date
    6/30/2010 - 14 years ago
  • Program Officer Name
    CHO, DAVID
  • Budget Start Date
    7/1/2007 - 17 years ago
  • Budget End Date
    6/30/2010 - 14 years ago
  • Fiscal Year
    2007
  • Support Year
    2
  • Suffix
  • Award Notice Date
    8/23/2007 - 17 years ago
Organizations

Novel Protein Adjuvant

[unreadable] DESCRIPTION (provided by applicant): Anti-bioterror vaccines will likely be based on recombinant proteins, synthetic peptides or DNA, and will probably require potent immunological adjuvants in order to render them effective. CD40 antibody conjugated to antigen has a very strong adjuvant effect, but such conjugates pose problems in terms of reproducible production, and because of the generation of antibody responses against the CD40 mAb itself, which may limit its effectiveness when used with subsequent immunisations. A number of alternative CD40 binding proteins have emerged, which should have similar potent adjuvant effects, but offer the advantage that they can be produced as straightforward, monomeric, in-frame fusions with the vaccine antigen. In addition, the number of these proteins available, having very little amino-acid homology with each other, means that different adjuvant proteins could be used with different vaccinations, thus circumventing the potential negative effect of anti-adjuvant responses on adjuvanticity. The project described here will provide proof of principle with up to three of this group of CD40 binding proteins, produced as recombinant chimeric fusions with the hemagglutinin of A/PR/8/34 influenza virus. The fusion proteins will be delivered via DNA vaccines, and in one case at least also as a recombinant protein vaccine. Hemagglutinin will be used as a model bioterror antigen, as influenza virus is a potential bioterror agent. However, this group of novel adjuvants will be widely applicable for use with a range of recombinant protein and DNA vaccines. Potential side effects, such as induction of IgE and polyclonal antibody responses will be assessed. Positive adjuvant effects will be assessed on antibody and T cell responses, as well as by challenge studies with live influenza virus. The proposed research may demonstrate the usefulness of this novel technique to enhance the immunogenicity of both DNA and protein based vaccines. The research therefore is applicable to the improvement of public health, not just in terms of protection against bioterrorism, but also in protection against naturally occurring infectious diseases, and possibly also in therapeutic vaccination for cancer. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R21
  • Administering IC
    AI
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    157302
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    855
  • Ed Inst. Type
  • Funding ICs
    NIAID:157302\
  • Funding Mechanism
  • Study Section
    VMD
  • Study Section Name
    Vaccines Against Microbial Diseases Study Section
  • Organization Name
    UNIVERSITY OF SHEFFIELD
  • Organization Department
  • Organization DUNS
    228147328
  • Organization City
    SHEFFIELD
  • Organization State
  • Organization Country
    UNITED KINGDOM
  • Organization Zip Code
    S10 2GW
  • Organization District
    UNITED KINGDOM