Technology ID
TAB-2773
Diagnostic Antigens for the Identification of Latent Tuberculosis Infection
E-Numbers
E-249-2013-1
E-249-2013-2
Lead Inventor
Quinn, Frederick (CDC)
Co-Inventors
Deslauriers, Manon (CDC)
Birkness, Kristin (CDC)
King, Peter (CDC)
Beall, Bernard (CDC)
Applications
Vaccines
Research Materials
Occupational Safety and Health
Diagnostics
Consumer Products
Therapeutic Areas
Infectious Disease
Immunology
Geriatrics
Development Stages
Pre-Clinical (in vitro)
Development Status
- In vitro data available
- In vivo data available (human)
Research Products
Antibodies
Lead IC
CDC
ICs
CDC
CDC researchers have developed technology for sero-diagnosis of typically symptomless latent stage tuberculosis disease, posing a threat to individuals under immunosuppressive or anti-inflammatory therapies. Specifically, this diagnostic approach exploits M. tuberculosis secreted latency specific antigens, such as alpha-crystallin, in the blood or urine of patients. This type of test could easily be developed into an inexpensive dip-stick format with high specificity (no cross-reactivity with other mycobacteria), rapidity, and sensitivity (fewer bacteria needed for a positive identification). Because secreted antigens are recognized more readily by the immune system, serum-derived antibodies to these antigens can correspondingly be used for diagnostic or research use.
Commercial Applications
- Development of a latent tuberculosis diagnostic
- Improvements to current diagnostics
- Public health/tuberculosis monitoring programs
- Screening elderly patients before beginning anti-inflammatory and/or anti-arthritis therapy
Competitive Advantages
- Rapid and inexpensive diagnostic for latent stage tuberculosis
- Specific for latent form, unlike current IGRA/TST diagnostics
- Easily developed as a cost effective dip-stick test
- Provides high specificity (no cross-reactivity with other mycobacteria) and sensitivity (fewer bacteria needed for a positive identification)
Licensing Contact: