SBIR-STTR Award

Microrna- and Autoantibody-Based Multiplex Assay for Systemic Lupus Erythematosus
Award last edited on: 10/19/16

Sponsored Program
SBIR
Awarding Agency
NIH : NIAMS
Total Award Amount
$150,000
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Taiho Kim

Company Information

Nesher Technologies Inc (AKA: NTI)

2100 W. 3rd Street
Los Angeles, CA 90057
   (213) 989-7418
   info@neshertech.com
   www.neshertech.com
Location: Single
Congr. District: 34
County: Los Angeles

Phase I

Contract Number: 1R43AR068888-01
Start Date: 8/1/15    Completed: 1/31/16
Phase I year
2015
Phase I Amount
$150,000
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with worldwide distribution. Despite medical treatment, morbidity and mortality from renal disease are still common in lupus patients. However, early diagnosis and prompt treatment can significantly improve long-term prognosis. Anti-double stranded (ds) DNA autoantibodies are a serologic hallmark of patients with SLE. In addition, circulating microRNAs (miRNAs) have been shown recently to be systematically altered, unveiling miRNA signatures with diagnostic utility. Growing evidence suggests that a multi-marker strategy, containing a combination of biomarkers with high clinical sensitivity and specificity, may enhance diagnostic and prognostic accuracy in the future compared to single marker tests. To support efforts of identifying the most informative biomarker panels, reliable next- generation platform technologies are needed that permit multiplexed detection of both protein and nucleic acid targets in small samples and are suitable for automation and integration into the clinical laboratory work flow. Nesher Technologies, Inc. (NTI) has exclusively licensed the intellectual property for an ultrasensitive and - specific biodetection technology, developed at the UCLA Single Molecule Biophysics Lab (headed by Prof. Shimon Weiss), with high single-well multiplexing potential, minimal sample requirements, and simplified handling procedures (no separation/washing and amplification steps). It is based on alternating laser excitation (ALEX) single molecule fluorescence spectroscopy, whereby target recognition molecules are tagged with different color fluorescent dyes (and quenchers). NTI recently achieved extension from 2-color to 4-color ALEX, substantially expanding its multiplexing power, and demonstrated diagnostic utility for direct protein as well as miRNA quantification. Furthermore, recent work by Profs. Steve Quake and Shimon Weiss shows i) combination of microfluidics-based sample handling with ALEX spectroscopy, termed "single molecule optofluidics", and ii) enhanced throughput using a multi-foci excitation/detection geometry. NTI's long-term goal is to develop rapid, highly multiplexed, ultrasensitive and -specific, as well as fully automated, nucleic acid- and protein-based diagnostic tests that require minimal sample sizes. Here, we propose assay development and clinical validation of a next-generation test with significantly improved diagnostic, prognostic, and treatment- guiding properties, implementing a panel of autoantibody and miRNA biomarkers, and overcoming limitations of current SLE testing. Our Specific Aims are: 1. Initial reagent development for a multiplex miRNA & autoantibody-based next-generation test for SLE 2. Separate as well as multiplexed biomarker detection and quantification using spiked samples 3. ALEX-based analysis of 42 archived clinical samples and cross-validation to ELISA and qPCR methods SBIR Phase II will propose assay expansion to include more markers, miniaturization, and development of a user-friendly, "sample in - answer out" diagnostic system offering significant cost and patient sample savings.

Public Health Relevance Statement:


Public Health Relevance:
Systemic lupus erythematosus (SLE), an autoimmune disease with an unpredictable course involving flares and remissions adversely affecting organ functions, remains associated with an appreciably shortened life span. As current single-marker tests for SLE are inadequate, there will be a great need for a versatile next- generation platform technology to detect and quantify panels of diagnostic and prognostic protein and nucleic acid biomarkers as they become available, in order to better assist in establishing early diagnosis of SLE, refine prognosis, guide management, target treatment, and finally improve patient survival. Based on patent- protected alternating laser excitation (ALEX) single molecule fluorescence spectroscopy, Nesher Technologies, Inc. intends to make its single molecule detection (SMD) platform technology robust and easy to use for diagnostic labs as well as the broad research community, and proposes to develop a next-generation test for SLE, monitoring a panel of microRNA and autoantibody biomarkers present in very small patient samples, thereby translating cutting-edge innovations in nanobiotechnology into benefits for the society at large by saving human lives and reducing healthcare costs.

NIH Spending Category:
Autoimmune Disease; Bioengineering; Biotechnology; Lupus; Prevention

Project Terms:
Acute Disease; Affect; Affinity; Antibodies; Antinuclear Antibodies; Antiphospholipid Antibodies; Archives; Area; Autoantibodies; Autoimmune Diseases; Automation; base; Binding (Molecular Function); Biological Assay; Biological Markers; Biophysics; Blinded; Body Fluids; circulating microRNA; Clinical; clinical assay development; Clinical Sensitivity; Color; Communities; Complex; Conduct Clinical Trials; cost; Detection; Development; Diagnosis; Diagnostic; diagnostic panel; Diagnostic tests; Disease remission; DNA; ds-DNA; Dyes; Early Diagnosis; Energy Transfer; Enzyme-Linked Immunosorbent Assay; Evaluation; Evaluation Studies; Exclusion; Flare; Fluorescence; Fluorescence Spectroscopy; Fluorescent Dyes; fluorophore; Future; Geometry; Goals; Head; Health Care Costs; Human; Immune; improved; Individual; innovation; Intellectual Property; interest; Kidney Diseases; Kinetics; Label; Laboratories; Lasers; Legal patent; Licensing; Longevity; Lupus; Measures; Medical; Methodology; Methods; Microfluidics; MicroRNAs; Miniaturization; Monitor; Morbidity - disease rate; Mortality Vital Statistics; nanobiotechnology; nanolitre; next generation; Noise; novel marker; novel therapeutics; Nucleic Acids; Organ; Outcome; outcome forecast; Pathogenesis; Patient Monitoring; Patients; Phase; Plasma; Procedures; prognostic; Property; prospective; Proteins; prototype; public health relevance; Reagent; Research; research clinical testing; Research Design; Risk; sample collection; Sample Size; Sampling; Savings; Sensitivity and Specificity; Serological; single molecule; Site; Small Business Innovation Research Grant; Societies; Solutions; Sorting - Cell Movement; Spectrum Analysis; Stratification; System; systemic autoimmune disease; Systemic Lupus Erythematosus; Technical Expertise; Technology; Testing; Therapeutic immunosuppression; Time; tool; Translating; Tumor Markers; user-friendly; Validation; virtual; Wor

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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