SBIR/STTR Research Award

DEVELOPMENT OF A VIRUS VECTOR VACCINE AGAINST ANTHRAX

Award identifier 9b30d9feaa7f7c1f5a63c79e3a7bdcd5ac22e0bf578777e0928b15b5991e0242Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$140,710

Program and phase

SBIR · 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
VIRRX, 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): The events on and following September 11, 2001 have revealed our nation's vulnerability to terrorist attacks. Although much talked about during the past decade, the threat of a bioterrorist attack against the United States was not realized until the intentional distribution of weapons grade Bacillus anthracis via the U.S. postal service. These attacks combined with questions concerning the safety of the current vaccine against B. anthracis warrant the rapid development of a new B. anthracis vaccine that is both safe and effective. Using the most recent technological advances in vaccine research, a novel vaccine will be developed that relies upon simultaneous expression of mutant forms of B. anthracis Protective Antigen (PA) and Lethal Factor (LF) in each of two different types of viral vectors. The first vector will be based on vaccinia virus, the virus that was used to eradicate smallpox. The MVA strain of vaccinia virus will be used to construct the vector inasmuch as this strain is attenuated and has been proven to be safe in humans. The second vector will be based on a replication-competent adenovirus vector, allowing high-level expression of the target antigens. A number of vaccine and cancer gene therapy vectors have been developed using replication-competent adenoviruses, emphasizing their safety in humans. The vaccinia- and adenovirus-based vectors will be evaluated individually and in combination for their ability to induce humoral and cell-mediated immune responses in a mouse model. It is anticipated that a prime and boost protocol in which the mice are first immunized with one vector and then immunity is boosted using the second vector will be most effective at generating a robust immune response to the PA and LF antigens. It is anticipated that in a Phase II application, the ability of these two vectors to protect from B. anthracis challenge will be assessed.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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