SBIR/STTR Research Award

Novel Delivery of a New Vaccine for Tuberculosis

Award identifier 4a60a1b88f8e3945883e26b2aa1b1ade50f8e8ba76a8310609602b8f6a2378f5Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$189,617

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
MYCOS RESEARCH, LLC
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): Tuberculosis is responsible for the death of over 3.3 million people each year, which is more than any other infectious agent. The current vaccine for tuberculosis is the BCG vaccine. BCG has been proven safe and effective at protecting young children, it is relatively inexpensive to produce, and it requires only a single immunization. Unfortunately, protecting adults from pulmonary disease with the BCG vaccine has been variably efficacious. As a result, the effort to produce a novel and efficacious vaccine for tuberculosis has intensified over the last decade. In the mouse model, the combination of a TH1 stimulating adjuvant and a M. tuberculosis derived recombinant fusion construct (Corixa Corporation) has resulted in a approximately 2 log decrease in bacterial burden following an aerogenic challenge with M. tuberculosis (approaching the level seen with the BCG vaccine). This vaccine formulation has also been effective in the guinea pig and cynomolgus monkey models of tuberculosis. This application proposes to investigate the ability of a transcutaneous immunization (TCI) to deliver this vaccine formulation to mice. The effectiveness of TCI has been demonstrated in pre-clinical and clinical trials and has been shown to induce both serum and mucosal humoral responses as well as cellular immune responses. The success of this novel delivery method will be evaluated by its ability to induce the development of a TH1 immune response and to provide a significant level of protection following a low dose aerosol challenge with M. tuberculosis. If successful, the advantages of transcutaneously delivering a vaccine for tuberculosis would be the lack of a needle injection, the simplicity of administration (especially in developing countries where tuberculosis is endemic), and the potential for using a lower dose of specific antigen, which would decrease the cost of vaccination.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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