Qualification of the Hemagglutination Inhibition Assay in Support of Pandemic Influenza Vaccine Licensure

Author:

Noah Diana L.123,Hill Heather123,Hines David123,White E. Lucile123,Wolff Mark C.123

Affiliation:

1. Southern Research Institute, 2000 9th Avenue South, Birmingham, Alabama

2. EMMES Corporation, 401 North Washington St., Suite 700, Rockville, Maryland 20850

3. CBR International Corporation, 2905 Wilderness Place, Suite 202, Boulder, Colorado 80301

Abstract

ABSTRACT Continued outbreaks of highly pathogenic avian influenza over the past decade have spurred global efforts to develop antivirals and vaccines. As part of vaccine development, standard methods are needed for determining serum antibody titers in response to vaccination. Hemagglutination inhibition (HAI) assays are appropriate for assessing the immunogenicity of pandemic influenza vaccines in support of license approval. We demonstrate that a rigorous qualification of the HAI assay for H5N1 influenza virus, evaluating for precision, intermediate precision, linearity, range, specificity, and robustness, satisfies the intent of regulatory guidance for assay validation despite the lack of availability of specific reference standard antigens and antisera.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

Reference7 articles.

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5. Stephenson, I., J. M. Wood, K. G. Nicholson, A. Charlett, and M. C. Zambon. 2004. Detection of anti-H5 responses in human sera by HAI using horse erythrocytes following MF59-adjuvanted influenza A/Duck/Singapore/97 vaccine. Virus Res.103:91-95.

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