Dengue Reporter Virus Neutralization Assay for Clinical Studies

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$2,649,021.00
Award Year:
2007
Program:
STTR
Phase:
Phase II
Contract:
2R42AI062100-03
Award Id:
71124
Agency Tracking Number:
AI062100
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
INTEGRAL MOLECULAR, 3701 MARKET ST, STE 340, PHILADELPHIA, PA, 19104
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
034055645
Principal Investigator:
EVA HARRIS
(510) 642-4845
EHARRIS@BERKELEY.EDU
Business Contact:
() -
bdoranz@integralmolecular.com
Research Institute:
REGENTS OF THE UNIVERSITY OF CALIFORNIA

UNIVERSITY OF CALIFORNIA BERKELEY
2150 Shattuck Avenue, Room 313
BERKELEY, CA, 94704 5940

Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): Dengue virus (DENV) is the most significant cause of arthropod-borne viral disease in humans, resulting in an estimated 50 million cases of dengue fever and over 450,000 cases of life-threatening dengue hemorrhagic feve r/dengue shock syndrome (DHF/DSS) each year. DENV has spread alarmingly across the globe over the past few decades, resulting in a dramatic increase in the number of dengue cases. As a result, DENV is now classified as a Category A pathogen of interest to the NIH. An effective dengue vaccine is critically needed, but has proven a significant challenge to develop because low affinity or low concentration antibodies that do not neutralize DENV can instead enhance infection. Thus, a vaccine that does not confe r persistent protection against all four serotypes of the virus is potentially dangerous to recipients if they are subsequently infected. Large-scale human trials of several tetravalent dengue vaccines are imminent, but reliable, high- throughput tools for measuring protective humoral immunity in these trials are still lacking. The primary assay for detecting neutralizing antibodies in human serum is the plaque reduction neutralization test (PRNT). PRNT is poorly suited for measuring the magnitude, persiste nce, and specificity of the humoral response in large- scale vaccine trials. Analysis of large numbers of serum samples would be greatly facilitated by the availability of a new, quality-controlled, automated method to test for neutralizing antibodies spec ific for each DENV serotype. In response to this need, we developed the dengue reporter virus particle (DENV RVP) which can be used to monitor infection of cells in culture and to detect the presence of neutralizing antibodies in a test sample. We expect c ommercial DENV RVPs to be used in vaccine trials, clinical studies, and basic dengue research. To complete the development and validation of the DENV RVP, our Specific Aims are: Validate RVPs for use in clinical studies Verify suitability of RVPs f or use in dengue vaccine trials Develop advanced production, quality control, and modifications of RVPs for clinical and research applications The global distribution of dengue virus is spreading rapidly - there are already 3 billion people (50 % of the world's population) living at risk of infection, resulting in more than 50 million cases of illness each year, making it the most significant arthropod-borne viral pathogen of humans. Vaccine development and epidemiological surveillance and contro l programs are hampered by the lack of a rapid, easy method for measuring protective humoral immunity. The product that will result from this proposal, a kit containing the dengue reporter virus particle (DENV RVP), will be the first safe, high-throughput, standardized assay of DENV neutralizing antibodies, and the most immediate public health impact of its use by customers will be accelerating tetravalent vaccine efficacy trials.

* information listed above is at the time of submission.

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