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Vaccine Response and Efficacy Studies

Focus on Flu Responding to the 2009 H1N1 pandemic Spring 2009 opened with a global threat – the first pandemic flu in 40 years for which there was no known public immunity. The novel H1N1 influenza A virus challenged public health professionals and diagnosticians across the globe. Focus Diagnostics, Quest Diagnostics' infectious disease company, introduced the first commercially available diagnostic test in the United States within weeks of the announcement. Focus worked closely with vaccine developers responding to a global flu strain emerging outside the normal course of seasonal influenza.

Standardized with WHO and CDC reference methods Custom assay development and validation ILI and Efficacy studies

  • HAI (hemagglutination inhibition)
  • Microneutralization
  • Antigen Validation
  • SRH (single radial hemolysin

  • Antibody subclasses
  • Multianalyte assays
  • Functional assays

  • Real-time PCR
  • Subtyping PCR
  • Culture (rapid and conventional)
  • Genotyping (sequencing)
  • Strain typing
  • Antiviral phenotyping

Vaccine Response Studies

Vaccine/Pathogen

Testing Method

Smallpox (vaccinia)

Microneutralization

Japanese Encephalitis Virus PRNT
Influenza (flu) vaccine(s) Hemagglutination inhibition
Poliovirus Viral neutralization
Pneumococcus Opsonophagocytosis
West Nile Virus PRNT, IFA
St. Louis Encephalitis Virus, La Crosse Virus PRNT, IFA
First FDA Clearance of a 2009 H1N1 Test Given to Focus Diagnostics


FDA Issues Another Emergency Use Authorization for Commercial H1N1 Flu Test to Quest Diagnostics’ Focus Diagnostics


Focus Diagnostics provides the first commercial test for detecting the 2009 H1N1 influenza virus that the FDA has authorized for emergency use.


 
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