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dc.creatorKontopoulou K., Ainatzoglou A., Ifantidou A., Nakas C.T., Gkounti G., Adamopoulos V., Papadopoulos N., Papazisis G.en
dc.date.accessioned2023-01-31T08:44:05Z
dc.date.available2023-01-31T08:44:05Z
dc.date.issued2021
dc.identifier10.1099/JMM.0.001387
dc.identifier.issn00222615
dc.identifier.urihttp://hdl.handle.net/11615/75092
dc.description.abstractReal-world data regarding the effectiveness, safety and immunogenicity of the Pfizer-BioNTech BNT162b2 mRNA vaccine are accumulating in the literature, suggesting that this vaccine generates high titres of S1-binding IgG antibodies that exhibit potent virus neutralization capacity. This is the first phase IV immunogenicity study to recruit a large number of Greek healthcare workers (n=425) including 63 previously-infected subjects. We measured titres of neutralizing IgGs against the receptor-binding domain of the S1 subunit of the spike protein of SARS-CoV-2 14 days post-immunization with the first dose, employing the SARS-CoV-2 IgG II Quant assay. A total of 92.24 % of our study cohort received a positive assay outcome and titres varied with age. Post-hoc analysis revealed that although titres did not significantly differ among participants aged 20-49 years, a significant decline was marked in the age group of 50-59 years, which was further accentuated in subjects aged over 60. Antibody titres escalated significantly among the previously-infected, indicating the potential booster effect of the first dose in that group. © 2021 The Authors.en
dc.language.isoenen
dc.sourceJournal of Medical Microbiologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85114089219&doi=10.1099%2fJMM.0.001387&partnerID=40&md5=65eb48ac6739a2cf3c03e59c35582d26
dc.subjectbnt 162b 2en
dc.subjectcomirnatyen
dc.subjectimmunoglobulin Gen
dc.subjectmessenger RNAen
dc.subjectneutralizing antibodyen
dc.subjectvirus spike proteinen
dc.subjectbnt 162 vaccineen
dc.subjectadulten
dc.subjectantibody titeren
dc.subjectArticleen
dc.subjectchillen
dc.subjectcohort analysisen
dc.subjectcontrolled studyen
dc.subjectcoronavirus disease 2019en
dc.subjectdrug efficacyen
dc.subjectdrug safetyen
dc.subjectevidence based practiceen
dc.subjectfatigueen
dc.subjectfemaleen
dc.subjectfeveren
dc.subjectGreeceen
dc.subjectheadacheen
dc.subjecthealth care personnelen
dc.subjecthumanen
dc.subjecthumoral immunityen
dc.subjectimmunizationen
dc.subjectinjection site painen
dc.subjectmaleen
dc.subjectmiddle ageden
dc.subjectmyalgiaen
dc.subjectoutcome assessmenten
dc.subjectreceptor bindingen
dc.subjectSevere acute respiratory syndrome coronavirus 2en
dc.subjectvaccine immunogenicityen
dc.subjectyoung adulten
dc.subjectadministration and dosageen
dc.subjectageden
dc.subjectdiagnosisen
dc.subjectepidemiologyen
dc.subjecthealth care personnelen
dc.subjectimmunologyen
dc.subjectprevention and controlen
dc.subjectreceiver operating characteristicen
dc.subjectvaccinationen
dc.subjectvirologyen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectCOVID-19en
dc.subjectCOVID-19 Vaccinesen
dc.subjectFemaleen
dc.subjectGreeceen
dc.subjectHealth Personnelen
dc.subjectHumansen
dc.subjectImmunogenicity, Vaccineen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectOutcome Assessment, Health Careen
dc.subjectROC Curveen
dc.subjectSARS-CoV-2en
dc.subjectVaccinationen
dc.subjectYoung Adulten
dc.subjectMicrobiology Societyen
dc.titleImmunogenicity after the first dose of the BNT162b2 mRNA Covid-19 vaccine: Real-world evidence from Greek healthcare workersen
dc.typejournalArticleen


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