Co-Inventors
Kristin Birkness (CDC)
Manon Deslauriers (CDC)
Peter King (CDC)
Development Status
- In vitro data available
- In vivo data available (human)
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)