The principal objective of this research plan is to demonstrate the effectiveness of a unique antigen delivery system as a vaccine/adjuvant to stimulate an immune response to influenza epitopes. The vaccine/adjuvant to be tested consists of an antigenic fusion protein formulated in an immunogenic liposome. The principal objectives of this project are to: construct the liposomal influenza epitope vaccine and; verify the immunogenicity of the vaccine design for both systemic and mucosal immunization. If successful, this novel vaccine/adjuvant technology should allow: (1) the commercial production of large quantities of purified immunogen using standard protein isolation techniques; (2) maximum flexibility for the insertion of single or multiple epitopes within a standard gene cassette for the rapid development of new vaccines; (3) easy incorporation of the antigen protein into liposomes, resulting in a commercially viable process for large-scale vaccine production and; (4) elimination of adverse side effects associated with the use of killed or modified live bacterial or viral vaccines. If successful, this vaccine/adjuvant system could have widespread implications for the treatment of numerous diseases caused by viral pathogens including influenza.

Proposed Commercial Applications

The potential commercial advantages of this vaccine and for any other vaccines developed using this approach include: a high margin of safety because the vaccine is non-pathogenic with minimal toxicity; relatively straightforward manufacturing procedures which make this process less costly; and efficacy comparable to virus- based vaccines. The proposed technology is also flexible; new vaccines can be made quickly and easily by simply """"""""cutting and pasting"""""""" new antigen sequences at the proper sites in the expression vector. Given the ability to rapidly design and engineer new vaccines, the potential commercial applications for this technology range from pathogenic diseases to cancers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43AI044579-01
Application #
2793431
Study Section
Special Emphasis Panel (ZRG2-SSS-4 (02))
Program Officer
Lambert, Linda C
Project Start
1999-03-15
Project End
2000-09-14
Budget Start
1999-03-15
Budget End
2000-09-14
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Molecular Express, Inc.
Department
Type
DUNS #
City
Rancho Dominguez
State
CA
Country
United States
Zip Code
90220
Fujii, Gary; Ernst, William; Adler-Moore, Jill (2008) The VesiVax system: a method for rapid vaccine development. Front Biosci 13:1968-80
Ernst, William A; Kim, Hyung J; Tumpey, Terrence M et al. (2006) Protection against H1, H5, H6 and H9 influenza A infection with liposomal matrix 2 epitope vaccines. Vaccine 24:5158-68