Reproducibility of Serologic Assays for Influenza Virus A (H5N1)
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Public Domain
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Aug 2009
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File Language:
English
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Alternative Title:Emerg Infect Dis
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Description:Hemagglutination-inhibition (HI) and neutralization are used to evaluate vaccines against influenza virus A (H5N1); however, poor standardization leads to interlaboratory variation of results. A candidate antibody standard (07/150) was prepared from pooled plasma of persons given clade 1 A/Vietnam/1194/2004 vaccine. To test human and sheep antiserum, 15 laboratories used HI and neutralization and reassortant A/Vietnam/1194/2004, A/turkey/Turkey/1/2005 (clade 2.2), and A/Anhui/1/2005 (clade 2.3.4) viruses. Interlaboratory variation was observed for both assays, but when titers were expressed relative to 07/150, overall percentage geometric coefficient of variation for A/Vietnam/1194/2004 was reduced from 125% to 61% for HI and from 183% to 81% for neutralization. Lack of reduced variability to clade 2 antigens suggested the need for clade-specific standards. Sheep antiserum as a standard did not reliably reduce variability. The World Health Organization has established 07/150 as an international standard for antibody to clade 1 subtype H5 and has an assigned potency of 1,000 IU/ampoule.
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Subjects:
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Source:Emerg Infect Dis. 15(8):1250-1259.
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Document Type:
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Name as Subject:
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Volume:15
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Issue:8
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Main Document Checksum:urn:sha256:5f2fb930f732ca43871eadb60e9de9182d2501b3e3a582ca606ed1ee48be15b7
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File Type:
Supporting Files
File Language:
English
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Emerging Infectious Diseases