SBIR/STTR Research Award

IMMUNO-ENHANCEMENT OF SKIN PATCH ANTHRAX VACCINATION

Award identifier 120b1036174d3b692337c6f46c9e79db455580d14b86cf07561452d5c8fda362Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

STTR · Phase I

Award year

2002

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VAXIN INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): In the wake of bio-terrorism, anthrax has become a real concern for public. Anthrax is listed as a category A biological disease by the CDC. Inhalation of anthrax spores can result in death due to rapid fatal hemorrhage. Since anthrax aerosol is odorless, invisible and easily spread, the most effective way to protect people from infection is vaccination. Skin patch vaccination with replication-incompetent recombinant adenovirus which is genetically engineered to encode pathogen antigens is a non-invasive, effective, safe and economical technology for vaccination. Recently, Vaxin, Inc. has generated recombinant adenovirus encoding anthrax protective antigen (PA), which can be used for skin patch anthrax vaccination. An important issue for the induction of protective responses is the efficacy of skin patch vaccination, which is dependent on the development of immune responses. Dendritic cells (DC) in the skin play a major role in the induction of immune responses to vaccinated antigens. Cutaneous application of vaccines induces DC migration from the skin to the spleen and regional lymph node where DC present vaccine antigens to lymphocytes and induce immune responses. Our recent studies have demonstrated that Slit2, a soluble protein expressed in the skin, inhibits DC migration out of the skin. Application of a soluble receptor for Slit2, Robo, can increase DC migration and enhance immune responses to antigen stimulation on the skin. The hypothesis of this proposal is that application of soluble Robo can enhance the efficacy of skin patch antrax vaccination. This Phase I study will first investigate against anthrax. Second, the effect of recombinant adenovirus encoding the soluble Robo on the efficacy of the anthrax vaccine will be examined. Finally, the study will determine the mechanism by which Robo increases the efficacy of skin-patch anthrax vaccination. Both RoboN and the anthrax vaccine will be applied to the skin without needle injection, completion of the studies in this proposal will also provide a protocol for enhancing the skin-patch anthrax vaccination. Ultimately, this protocol may also be applied for skin-patch vaccines to other pathogens and tumor antigens.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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