SBIR/STTR Research Award

Topical adjuvants to enhance the efficacy of influenza vaccines

Award identifier 0a8aa74b5f77b6a10496c73b6fd1fb83744558b67fd999090654aad2fb35f5abAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,287,840

Program and phase

SBIR · Phase II

Award year

2010

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
LANCELL, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2010-2
Topic code
NIAID

Research abstract

DESCRIPTION (provided by applicant): An adequate medical response to the threat of pandemic influenza includes surveillance and isolation, a sufficient supply of effective antiviral drugs, and rapid development of a protective vaccine. Under optimal circumstances, production of enough vaccine to protect the US population would take 6 months. A lag time of 6 months between identification of a pandemic strain and an adequate supply of vaccine could result in devastating morbidity, mortality, and economic loss. A dose-sparing adjuvant that enabled a limited supply of vaccine to protect more people would diminish this problem. We have identified a small lipophilic molecule that can penetrate the intact stratum corneum and activate the dendritic cells (DC) in normal mouse skin. It enables resident DC to process adjuvant-free antigens injected into the skin and causes the DC to mature and migrate to the draining lymph node where they activate naove T cells. The speed with which this topical adjuvant increases protective antibody responses, its low cost, and physical independence of the vaccine antigen, suggest that it might be an ideal adjuvant for enhancing the protection afforded by a limiting supply of influenza vaccine. The aims of this Phase II application are to: 1) define the mechanism of action of this adjuvant; 2) determine the efficacy and optimize its use as a topical adjuvant for an influenza vaccine in miniature pigs as a model for human skin; 3) employ assays of transdermal transport across human skin ex vivo to optimize the conditions for its use as a topical adjuvant; and 4) perform pilot pre-clinical toxicity assays on this adjuvant. If our efforts are successful, the product will be an inexpensive small molecule, applied to the skin over a vaccine injection site that will make vaccines more effective. PUBLIC HEALTH RELEVANCE: The best public health response to pandemic influenza is an effective vaccine, but with current vaccine manufacturing capabilities it could take years to produce enough vaccine to protect the US population. We need vaccine additives that can extend the effective dose of a vaccine to cover more people. That is the goal of the proposed research.

Technology keywords

Not reported

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.