Technology ID
              TAB-2672
          Human Influenza Virus Real-time RT-PCR Detection and Characterization Panel
E-Numbers
          E-331-2013-0
              Lead Inventor
          Lindstrom, Stephen
              Lead IC
          CDC
              Co-Inventors
          Klimov, Alexander
          Cox, Nancy
          Loftin, Lamorris
              ICs
          CDC
              Applications
          Therapeutics
          Research Materials
          Occupational Safety and Health
          Diagnostics
          Consumer Products
              Therapeutic Areas
          Infectious Disease
              Development Stages
          Pre-Clinical (in vitro)
              Development Status
              In vitro data available
          This invention relates to methods of rapidly detecting influenza, including differentiating between type and subtype.  Unlike culture and serological tests requiring 5 to 14 days for completion, CDC researchers developed a rapid, accurate assay, which is easily adapted to kit form.  This assay also requires less labor input than immunoassays. These methods can be used to quickly identify a broad variety of influenza types and subtypes, including viruses that may be involved in pandemics (such as H5N1, for example).
      
  Commercial Applications
              - Influenza diagnostic using clinical specimens
- High-throughput screenings
- Influenza surveillance programs
Competitive Advantages
              - Already FDA approved
- Especially useful for H5N1 screening
- Sensitive detection
- Specific discrimination of influenza subtypes
- Easily formatted as kit or array
- Faster than culturing and serological identification methods
- Less laborious and more objective than immunoassays
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