SBIR-STTR Award

Development of a Peptidomic Rapid Point-Of-Care Tb Diagnostic
Award last edited on: 4/15/2019

Sponsored Program
STTR
Awarding Agency
NIH : NIAID
Total Award Amount
$1,560,055
Award Phase
2
Solicitation Topic Code
855
Principal Investigator
R Sam Niedbala

Company Information

TB Biosciences Inc

205 Webster Street
Bethlehem, PA 18015
   (800) 882-9923
   N/A
   www.tbbiosciences.com

Research Institution

New York University

Phase I

Contract Number: 1R41AI091049-01
Start Date: 7/1/2010    Completed: 6/30/2012
Phase I year
2010
Phase I Amount
$262,427
The goals of this proposal are to devise rapid serological tests that can replace the sputum smear test for the diagnosis of active TB and meets the WHO specifications to replace microscopy in resource-limited countries based on immunodominant peptides from three M. tb cell-wall proteins. Although direct smear microscopy is highly specific, the test is tedious, time-consuming, requires multiple patient visits before diagnosis, and has limited sensitivity. The Company's approach is based on the prior identification of three cell wall proteins of M. tuberculosis (PTRP, PE-PGRS51 and LipC) that are highly immunogenic in TB subjects, but not in individuals with latent TB infection (LTBI). The identified immunodominant epitopes were mapped and combinations of immunodominant peptides derived from these proteins are predicted to detect >95% of smear positive TB patients. Specifically we plan to devise microplate ELISA assay(s) based on the peptide combinations demonstrating maximum sensitivity and specificity for detection of anti- TB antibodies in sera, and to verify the performance of the assays with a panel of sera from cohorts of TB-negative subjects (Aim #1); to translate the microplate ELISA assay to a lateral flow point-of- care format using the 9 immunodominant individual peptides previously identified (Aim #2); and to identify the best peptide combination(s) to use in a multiplexed lateral flow device to result in maximum sensitivity and specificity. This assay will be validated with large-panels of clinical samples (Aim #3). During Phase 2, we plan to further validate and refine the rapid test with samples from diverse geographic sites and advance commercialization of both the microplate and rapid lateral flow assays. Testing will be performed with both serum and oral fluids samples. This will allow the Company to determine if it is necessary to have region-specific tests or if one combinatorial test is appropriate worldwide. The development of a non-invasive salivary and/or serum diagnostic test for active TB will fill an urgent need in resource-limited areas.

Public Health Relevance:
The work proposed will ultimately lead to development of an inexpensive, robust, and rapid diagnostic ELISA test and point-of-care device for active TB infections. No reliable rapid test for TB currently exists and this assay would represent a major advance.

Thesaurus Terms:
Afb; Aids Virus; Abbreviations; Acid Fast; Acid Fast Bacillae; Acid Fast Bacillae Staining Method; Acquired Immune Deficiency Syndrome Virus; Acquired Immunodeficiency Syndrome Virus; Antibodies; Antigenic Determinants, Immunodominant; Area; Assay; Bacillus; Bacillus (Bacterium); Bedside Testings; Bioassay; Biologic Assays; Biological Assay; Blood Serum; Caring; Cell Wall; Clinical; Country; Detection; Development; Devices; Diagnosis; Diagnostic; Diagnostic Tests; Directly Observed Therapy; Elisa; Emergencies; Emergency Situation; Enzyme-Linked Immunosorbent Assay; Foundations; Geographic Area; Geographic Locations; Geographic Region; Geographical Location; Goals; Hiv; Htlv-Iii; Heating; Human Immunodeficiency Viruses; Human T-Cell Leukemia Virus Type Iii; Human T-Cell Lymphotropic Virus Type Iii; Human T-Lymphotropic Virus Type Iii; Immunodominant Determinants; Immunodominant Domains; Immunodominant Epitopes; Immunodominant Regions; Immunodominant Sites; Individual; Infection; Lav-Htlv-Iii; Lateral; Lead; Lip; Lip Structure; Liquid Substance; Low Income; Lymphadenopathy-Associated Virus; M. Tb; M. Tuberculosis; M.Tb; M.Tuberculosis; Maps; Mesh Descriptors Class 4; Microscopic; Microscopy; Mycobacterial Infection; Mycobacterium Infections; Mycobacterium Tuberculosis; Oral; Patients; Pb Element; Peptides; Performance; Phase; Programs (Pt); Programs [publication Type]; Proteins; Reporting; Research Resources; Research Training; Resources; Salivary; Sampling; Sensitivity And Specificity; Serologic Tests; Serological Tests; Serum; Site; Sputum; Testing; Testings, Bedside; Time; Translating; Translatings; Tropical Disease; Virus-Hiv; Visit; Who; Wit; Work; World Health Organization; Base; Cohort; Combinatorial; Commercialization; Fluid; Gene Product; Geographic Site; Heavy Metal Pb; Heavy Metal Lead; Immunogenic; Innovate; Innovation; Innovative; Language Translation; Latent Infection; Liquid; Meetings; New Diagnostics; Next Generation Diagnostics; Novel Diagnostics; Point Of Care; Point Of Care Testing; Programs; Public Health Relevance; Serology; Success; Tool

Phase II

Contract Number: 5R41AI091049-02
Start Date: 7/1/2010    Completed: 1/31/2015
Phase II year
2011
(last award dollars: 2014)
Phase II Amount
$1,297,628

The goals of this proposal are to devise rapid serological tests that can replace the sputum smear test for the diagnosis of active TB and meets the WHO specifications to replace microscopy in resource-limited countries based on immunodominant peptides from three M. tb cell-wall proteins. Although direct smear microscopy is highly specific, the test is tedious, time-consuming, requires multiple patient visits before diagnosis, and has limited sensitivity. The Company's approach is based on the prior identification of three cell wall proteins of M. tuberculosis (PTRP, PE-PGRS51 and LipC) that are highly immunogenic in TB subjects, but not in individuals with latent TB infection (LTBI). The identified immunodominant epitopes were mapped and combinations of immunodominant peptides derived from these proteins are predicted to detect >95% of smear positive TB patients. Specifically we plan to devise microplate ELISA assay(s) based on the peptide combinations demonstrating maximum sensitivity and specificity for detection of anti- TB antibodies in sera, and to verify the performance of the assays with a panel of sera from cohorts of TB-negative subjects (Aim #1); to translate the microplate ELISA assay to a lateral flow point-of- care format using the 9 immunodominant individual peptides previously identified (Aim #2); and to identify the best peptide combination(s) to use in a multiplexed lateral flow device to result in maximum sensitivity and specificity. This assay will be validated with large-panels of clinical samples (Aim #3). During Phase 2, we plan to further validate and refine the rapid test with samples from diverse geographic sites and advance commercialization of both the microplate and rapid lateral flow assays. Testing will be performed with both serum and oral fluids samples. This will allow the Company to determine if it is necessary to have region-specific tests or if one combinatorial test is appropriate worldwide. The development of a non-invasive salivary and/or serum diagnostic test for active TB will fill an urgent need in resource-limited areas.

Public Health Relevance:
The work proposed will ultimately lead to development of an inexpensive, robust, and rapid diagnostic ELISA test and point-of-care device for active TB infections. No reliable rapid test for TB currently exists and this assay would represent a major advance.

Public Health Relevance Statement:
Narrative The work proposed will ultimately lead to development of an inexpensive, robust, and rapid diagnostic ELISA test and point-of-care device for active TB infections. No reliable rapid test for TB currently exists and this assay would represent a major advance.

NIH Spending Category:
Infectious Diseases; Rare Diseases; Tuberculosis

Project Terms:
Abbreviations; Acid Fast Bacillae Staining Method; Antibodies; Area; Bacillus (bacterium); base; Bedside Testings; Biological Assay; Caring; Cell Wall; Clinical; cohort; combinatorial; commercialization; Country; Detection; Development; Devices; Diagnosis; Diagnostic; Diagnostic tests; Directly Observed Therapy; Emergency Situation; Enzyme-Linked Immunosorbent Assay; Foundations; Geographic Locations; Goals; Heating; HIV; Immunodominant Epitopes; immunogenic; Individual; Infection; innovation; latent infection; Lateral; Lead; Lip structure; Liquid substance; Low income; Maps; meetings; Microscopic; Microscopy; Mycobacterium Infections; Mycobacterium tuberculosis; novel diagnostics; Oral; Patients; Peptides; Performance; Phase; point of care; programs; Proteins; public health relevance; Reporting; Research Training; Resources; Salivary; Sampling; Sensitivity and Specificity; Serologic tests; Serum; Site; Sputum; success; Testing; Time; tool; Translating; Tropical Disease; Visit; Wit; Work; World Health Organization