AVIRULENT SALMONELLA HOST VECTOR HUMAN VACCINE SYSTEMS

Information

  • Research Project
  • 2004148
  • ApplicationId
    2004148
  • Core Project Number
    R42AI036585
  • Full Project Number
    2R42AI036585-02
  • Serial Number
    36585
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/1/1994 - 31 years ago
  • Project End Date
    4/30/1999 - 26 years ago
  • Program Officer Name
  • Budget Start Date
    5/1/1997 - 28 years ago
  • Budget End Date
    4/30/1998 - 27 years ago
  • Fiscal Year
    1997
  • Support Year
    2
  • Suffix
  • Award Notice Date
    5/5/1997 - 28 years ago
Organizations

AVIRULENT SALMONELLA HOST VECTOR HUMAN VACCINE SYSTEMS

Our long-term goals are directed at developing recombinant avirulent Salmonella vaccines for oral administration to protect humans against bacterial, viral, mycotic and parasitic pathogens, especially those that colonize on or invade through mucosal surfaces. Toward this goal, we propose to expand the host-vector options for such recombinant vaccines in order to circumvent potential difficulties with repeat immunizations for one or several different recombinant avirulent Salmonella vaccines. The objectives of the research to be conducted during the phase I study include: 1) to introduce genetically defined chromosome deletion mutations that are known to render S. typhimurium and S. typhi avirulent and immunogenic in mice and humans, respectively, into Salmonella paratyphi A, S. paratyphi B (S. shottmuellerii) and S. paratyphi C (S. herschfeldii), and 2) to characterize these strains in comparison to S. typhimurium and S. typhi constructs for stability of mutant phenotype, growth rate, ability to attach to, invade, multiply in and transcytose cells in culture, and for avirulence and immunogenicity in mice. The objective during the phase II study will be to evaluate avirulence and immunogenicity of the S. paratyphi mutants in humans and to investigate utility as the host-vector component of recombinant vaccines to stimulate, following oral immunization, mucosal, humoral and cellular immunities.

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R42
  • Administering IC
    AI
  • Application Type
    2
  • 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
    ZRG5
  • Study Section Name
  • Organization Name
    MEGAN HEALTH, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    ST. LOUIS
  • Organization State
    MO
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    63110
  • Organization District
    UNITED STATES