Influenza Virus-like Particles As Vaccines

Information

  • Research Project
  • 7056094
  • ApplicationId
    7056094
  • Core Project Number
    R43AI063830
  • Full Project Number
    5R43AI063830-02
  • Serial Number
    63830
  • FOA Number
    PAS-02-149
  • Sub Project Id
  • Project Start Date
    5/1/2005 - 20 years ago
  • Project End Date
    12/31/2007 - 17 years ago
  • Program Officer Name
    CHO, DAVID
  • Budget Start Date
    5/1/2006 - 19 years ago
  • Budget End Date
    12/31/2007 - 17 years ago
  • Fiscal Year
    2006
  • Support Year
    2
  • Suffix
  • Award Notice Date
    6/26/2006 - 19 years ago
Organizations

Influenza Virus-like Particles As Vaccines

[unreadable] DESCRIPTION (provided by applicant): The long term objective of this proposal is to develop a novel cell-based system for creating influenza-virus like particle (VLP) vaccines against epidemic and potentially pandemic influenza viruses. This strategy will generate in a rapid and safe manner VLP structures that morphologically and biochemically resemble wild type virus, but are devoid of influenza genetic material and therefore non-infectious. Quadruple baculovirus recombinants will be used to express in insect cells the influenza structural proteins (M1, M2, HA, IMA) necessary for the formation and release of influenza VLPs from the cell surface. Replacement of the genes encoding the HA and NA, or both in the quadruple construct by those of the current epidemic (H3N2/Fujian) influenza virus or the HA and NA of influenza viruses with pandemic potential (H5N1, H7N7, and H1N1/1918) will allow us to create vaccines against these dangerous viruses in a safe manner. Candidate vaccines will be harvested and purified from the culture supernatant of insect cells infected with any of the four quadruple recombinants. The immunogenicity (local and systemic level) and protective efficacy elicited by these vaccines will be evaluated in mice and ferrets. Preliminary studies with a two component VLP vaccine in mice administered via either the intranasal or intramuscular route have demonstrated complete protection against a lethal influenza virus challenge. These results indicate the promise of this vaccine technology, which uses cell as production substrate, produces non-infectious entities, and is versatile enough to quickly accommodate emerging flu viruses. This will be a significant technological improvement in influenza vaccine production, and will facilitate the creation of vaccines against diverse influenza viruses and thereby protect the public from serious natural or perhaps intentional outbreaks of human influenza. [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R43
  • Administering IC
    AI
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    499800
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
    NIAID:499800\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    TECHNOVAX, INC.
  • Organization Department
  • Organization DUNS
    361464907
  • Organization City
    TARRYTOWN
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    105916702
  • Organization District
    UNITED STATES