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    A novel multiplex poliovirus binding inhibition assay applicable for large serosurveillance and vaccine studies, without the use of live poliovirus.

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    Authors
    Schepp, Rutger M
    Berbers, Guy A M
    Ferreira, José A
    Reimerink, Johan H
    van der Klis, Fiona R
    Type
    Article
    Language
    en
    
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    Title
    A novel multiplex poliovirus binding inhibition assay applicable for large serosurveillance and vaccine studies, without the use of live poliovirus.
    Published in
    J Virol Methods 2017, 241:15-23
    Publiekssamenvatting
    Large-scale serosurveillance or vaccine studies for poliovirus using the "gold standard" WHO neutralisation test (NT) are very laborious and time consuming. With the polio eradication at hand and with the removal of live attenuated Sabin strains from the oral poliovirus vaccine (OPV), starting with type 2 (as of April 2016), laboratories will need to conform to much more stringent laboratory biosafety regulations when handling live poliovirus strains. In this study, a poliovirus binding inhibition multiplex immunoassay (polio MIA) using inactivated poliovirus vaccine (IPV-Salk) was developed for simultaneous quantification of serum antibodies directed to all three poliovirus types. Our assay shows a good correlation with the NT and an excellent correlation with the ELISA-based binding inhibition assay (POBI). The assay is highly type-specific and reproducible. Additionally, serum sample throughput increases about fivefold relative to NT and POBI and the amount of serum needed is reduced by more than 90%. In conclusion, the polio MIA can be used as a safe and high throughput application, especially for large-scale surveillance and vaccine studies, reducing laboratory time and serum amounts needed.
    DOI
    10.1016/j.jviromet.2016.12.006
    PMID
    27988324
    URI
    http://hdl.handle.net/10029/620973
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jviromet.2016.12.006
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