Publication:
Detection of dengue cases by serological testing in a dengue vaccine efficacy trial: Utility for efficacy evaluation and impact of future vaccine introduction

dc.contributor.authorEric Plennevauxen_US
dc.contributor.authorArunee Sabchareonen_US
dc.contributor.authorKriengsak Limkittikulen_US
dc.contributor.authorPornthep Chanthavanichen_US
dc.contributor.authorChukiat Sirivichayakulen_US
dc.contributor.authorAnnick Moureauen_US
dc.contributor.authorMark Boazen_US
dc.contributor.authorT. Anh Wartelen_US
dc.contributor.authorMelanie Savilleen_US
dc.contributor.authorAlain Bouckenoogheen_US
dc.contributor.otherSanofi Pasteur SAen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSanofi Pasteuren_US
dc.contributor.otherClinical Sciences and Medical Affairs Asiaen_US
dc.date.accessioned2018-12-11T02:15:30Z
dc.date.accessioned2019-03-14T08:04:10Z
dc.date.available2018-12-11T02:15:30Z
dc.date.available2019-03-14T08:04:10Z
dc.date.issued2016-05-23en_US
dc.description.abstract© 2016 Elsevier Ltd. Background: Dengue diagnosis confirmation and surveillance are widely based on serological assays to detect anti-dengue IgM or IgG antibodies since such tests are affordable/user-friendly. The World Health Organization identified serological based diagnosis as a potential tool to define probable dengue cases in the context of vaccine trials, while acknowledging that this may have to be interpreted with caution. Methods: In a phase IIb randomized, placebo-controlled trial assessing the efficacy of a tetravalent dengue vaccine (CYD-TDV) in Thai schoolchildren, case definition was based on virological confirmation by either serotype-specific RT-PCRs or by NS1-antigen ELISA (Clinicaltrials.gov NCT00842530). Here, we characterized suspected dengue cases using IgM and IgG ELISA to assess their utility in evaluating probable dengue cases in the context of vaccine efficacy trials, comparing virologically-confirmed and serologically diagnosed dengue in the vaccine and placebo groups. Serologically probable cases were defined as: (1) IgM positive acute- or convalescent-phase samples, or (2) IgG positive acute-phase sample and ≥4-fold IgG increase between acute and convalescent-phase samples. Results: Serological diagnosis had good sensitivity (97.1%), but low specificity (85.1%) compared to virological confirmation. A high level of false positivity through serology diagnosis particularly in the 2 months post-vaccination was observed, and is most likely related to detection of the immune response to the dengue vaccine. This lack of specificity and bias with vaccination demonstrates the limitation of using IgM and IgG antibody responses to explore vaccine efficacy. Conclusion: Reliance on serological assessments would lead to a significant number of false positives during routine clinical practice and surveillance following the introduction of the dengue vaccine.en_US
dc.identifier.citationVaccine. Vol.34, No.24 (2016), 2707-2712en_US
dc.identifier.doi10.1016/j.vaccine.2016.04.028en_US
dc.identifier.issn18732518en_US
dc.identifier.issn0264410Xen_US
dc.identifier.other2-s2.0-84963936272en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/43098
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84963936272&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleDetection of dengue cases by serological testing in a dengue vaccine efficacy trial: Utility for efficacy evaluation and impact of future vaccine introductionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84963936272&origin=inwarden_US

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