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Biomarker discovery for immunodiagnosis of invasive candidiasis

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41AI108114-01
Agency Tracking Number: R41AI108114
Amount: $600,000.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NIAID
Solicitation Number: PA12-089
Timeline
Solicitation Year: 2013
Award Year: 2013
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
1664 N VIRGINIA ST
RENO, NV 89557-0001
United States
DUNS: 78634704
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 THOMAS KOZEL
 (775) 784-4124
 tkozel@dxdiscovery.com
Business Contact
 DAVID MAINE
Phone: (775) 223-6169
Email: dmaine@dxdiscovery.com
Research Institution
 UNIVERSITY OF NEVADA
 
Office of Sponsored Projects 204 Ross Hall Mailstop 325
RENO, NV 89557-
United States

 () -
 Nonprofit College or University
Abstract

DESCRIPTION (provided by applicant): Invasive candidiasis (IC) is one of the most serious threats to patients in a critical setting. With as many as 60,000 cases per year in the U.S., the total cost associated with IC in the U.S. may be as high as 2-4 billion/year. One of the most critical factors influencing patient outcome is early diagnosis. The goal of this project is a rapi and inexpensive immunoassay that will use serum as a sample to identify the presence of IC. This is an unmet need for diagnosis of candidiasis, particularly for tests near the point of patien care. The target population will be individuals for whom advanced medical intervention and use of potent cytotoxic drugs have led to a proliferation of deep-seated infection by Candida spp. Theoverall hypothesis is that protein antigens of Candida spp. are shed into blood in concentrations that would be biomarkers for disease. The approach will be immunoassay for the presence of two or more distinct antigens that i) are shared across Candida spp. that cause IC and ii) are shed into blood during infection. Simultaneous detection of multiple antigens will markedly enhance the predictive value. The product will be assays with the lateral flow immunoassay (LFI) and/or enzyme-linked immunoassay (ELISA) platforms. To date, we have used a novel biomarker discover process termed In vivo Microbial Antigen Discovery (InMAD) to identify 5 candidate proteins. Specific Aim 1 will repeat this experiment and identify at least 5 additional candidate biomarkers (total of 10 proteins). Aim 2 will confirm at least 5 proteins as genuine biomarkers using IC serum samples from animal models and humans. If Phase I is successful, a Phase II application would i) generate monoclonal antibodies to biomarker proteins, ii) construct prototype immunoassays in LFI or ELISA format and iii) perform pre-clinical studies for diagnosis of IC. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Invasive candidiasis (IC) is one of the most devastating complications of advancedmedical care and use of powerful immunosuppressive drugs. IC is difficult to diagnose and difficult to treat. This is a translational research study whose goal is n immunoassay for early, rapid, inexpensive and non-invasive diagnosis of IC. If successful,the project could dramatically reduce morbidity and mortality from invasive candidiasis through early diagnosis and treatment.

* Information listed above is at the time of submission. *

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