Injection of animals with naked DNA of mammalian expression vectors induces cellular and humoral immune responses against the encoded protein. We have demonstrated that introduction of naked DNA into the superficial skin induces long lasting humoral and cellular immune responses, which are not obtainable by conventional protein immunization. Furthermore, these immune responses can be modulated specifically by administration of cytokine genes.
The Specific Aims of the proposed experiments are: (1) to compare the efficacy of intradermal (i.d.) and intramuscular (i.m.) genetic immunization with different antigen/gene system in triggering cellular and humoral immunity. (2) to modulate immune responses by an """"""""immunological window"""""""" approach, i.e., by in vivo transfection of cytokine genes into a localized area of the superficial skin prior to delivery of the given protein antigen to the same site. (3) to elicit immune responses specific for TH1 or TH2 lymphocytes by conditioning the superficial ski with specific TH1 related cytokine genes (IL-2, IL-12, and INFgamma) or TH2 related cytokine genes (IL-4, IL-5, IL-6 and IL-10), respectively. (4) to induce a shift from an already established (committed) antigen specific TH2 response in vivo to a TH1 response, and vice versa, by applying the principals of the immunological window. The proposed studies will establish the basic principles of genetic immunization and of immune regulation by cytokine gene delivery using well defined animal models. The results should enable us to design strategies for genetic manipulation of human immune responses to infectious agents, allergens, autoantigens and tumor associated antigens.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI037305-02
Application #
2074002
Study Section
Special Emphasis Panel (SRC (58))
Project Start
1994-09-30
Project End
1997-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Spiegelberg, H L; Raz, E (1999) DNA based immunotherapeutics for allergy. Arb Paul Ehrlich Inst Bundesamt Sera Impfstoffe Frankf A M :283-90;discussion 291-2
Raz, E; Spiegelberg, H L (1999) Deviation of the allergic IgE to an IgG response by gene immunotherapy. Int Rev Immunol 18:271-89
Tighe, H; Corr, M; Roman, M et al. (1998) Gene vaccination: plasmid DNA is more than just a blueprint. Immunol Today 19:89-97
Lee, D J; Tighe, H; Corr, M et al. (1997) Inhibition of IgE antibody formation by plasmid DNA immunization is mediated by both CD4+ and CD8+ T cells. Int Arch Allergy Immunol 113:227-30
Roman, M; Martin-Orozco, E; Goodman, J S et al. (1997) Immunostimulatory DNA sequences function as T helper-1-promoting adjuvants. Nat Med 3:849-54
Spiegelberg, H L; Orozco, E M; Roman, M et al. (1997) DNA immunization: a novel approach to allergen-specific immunotherapy. Allergy 52:964-70
Raz, E (1997) Introduction: gene vaccination, current concepts and future directions. Springer Semin Immunopathol 19:131-7
Roman, M; Spiegelberg, H L; Broide, D et al. (1997) Gene immunization for allergic disorders. Springer Semin Immunopathol 19:223-32
Raz, E; Tighe, H; Sato, Y et al. (1996) Preferential induction of a Th1 immune response and inhibition of specific IgE antibody formation by plasmid DNA immunization. Proc Natl Acad Sci U S A 93:5141-5
Sato, Y; Roman, M; Tighe, H et al. (1996) Immunostimulatory DNA sequences necessary for effective intradermal gene immunization. Science 273:352-4