ATTENUATED SHIGELLA AS VECTOR FOR HELICOBACTER VACCINE

Information

  • Research Project
  • 2075049
  • ApplicationId
    2075049
  • Core Project Number
    R43AI038124
  • Full Project Number
    1R43AI038124-01
  • Serial Number
    38124
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/30/1995 - 29 years ago
  • Project End Date
    6/30/1996 - 28 years ago
  • Program Officer Name
  • Budget Start Date
    9/30/1995 - 29 years ago
  • Budget End Date
    6/30/1996 - 28 years ago
  • Fiscal Year
    1995
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/29/1995 - 29 years ago
Organizations

ATTENUATED SHIGELLA AS VECTOR FOR HELICOBACTER VACCINE

DESCRIPTION: (Adapted from the applicant's abstract) The goal of this study is to develop a live vector vaccine against Helicobacter pylori by expression of urease in attenuated Shigella flexneri 2A strains and testing the ability of these strains to induce a protective mucosal response against H. felis in mice. Helicobacter pylori ureases will be expressed in attenuated S. flexneri strains to assess the feasibility of Shigella as an oral vaccine vector. OraVax and others have demonstrated that oral immunization with H. pylori urease results in a protective response against H. felis infection in mice when administered along with Cholera Toxin as a mucosal adjuvant. Attenuated S. flexneri 2A (CVD1203) expressing urease will be constructed and used to immunize mice. Protective immunity to Helicobacter infection will be assessed by subsequent challenge with H. felis. The proposed experiments will evaluate the use of a live vector approach to immunization against H. pylori as an alternative to toxic mucosal adjuvants. The results of these preliminary experiments will provide the basis for Phase II experiments using non-human primate models of Shigella and H. pylori to confirm the efficacy of live attenuated S. flexneri 2A strains as vaccine live delivery vectors. PROPOSED COMMERCIAL APPLICATION: The development of an attenuated recombinant strain of Shigella with the ability to induce a high level mucosal immune response against the expressed foreign gene product could have high commercial potential. The devleopment of a vaccine directed towards preventing colonization by Helicobacter pylori could also have high commercial potential.

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
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG7
  • Study Section Name
  • Organization Name
    ACAMBIS, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    02139
  • Organization District
    UNITED STATES