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dc.creatorVoulgaridi I., Sarrou S., Dadouli A., Peristeri A.-M., Nasika A., Onoufriadis I., Kyritsi M.A., Anagnostopoulos L., Theodoridou A., Avakian I., Pappa D., Konstantinou A.-K., Papadamou G., Mouchtouri V.A., Petinaki E., Speletas M., Hadjichristodoulou C.en
dc.date.accessioned2023-01-31T11:37:14Z
dc.date.available2023-01-31T11:37:14Z
dc.date.issued2022
dc.identifier10.3390/vaccines10081268
dc.identifier.issn2076393X
dc.identifier.urihttp://hdl.handle.net/11615/80751
dc.description.abstractThe aim of the study was to compare mRNA vaccine BNT162b2 with adenovirus vector- based vaccines in terms of presence of adverse reactions, immunogenicity, and protection against COVID-19. A total of 270 individuals were enrolled, of which 135 were vaccinated with adenovirus vector-based vaccines and compared with 135 age- and sex-matched participants who received the BNT162b2 mRNA vaccine. Serum sampling was performed on all participants on days 21, 42, 90, and 180 following the first dose, to evaluate anti-spike IgG and IgA responses. Antibodies were quantified by chemiluminescent microplate and ELISA assays. We demonstrate that both mRNA and adenovirus vector-based vaccines caused mild side-effects and were effective in inducing adequate antibody responses against SARS-CoV-2, although BNT162b2 was superior concerning the intensity of antibody responses and protection against severe COVID-19. Moreover, we identify that IgG and IgA responses depended primarily on both history of previous COVID-19 infection and vaccination platform used, with individuals immunized with a single-dose vaccine having lower antibody titers over time. Lastly, all vaccine platforms had limited side-effects, with the most frequent pain at the injection site. Our results provide useful information regarding antibody responses after vaccination with different vaccine platforms, which can be useful for public health vaccination strategies. © 2022 by the authors.en
dc.language.isoenen
dc.sourceVaccinesen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85137408713&doi=10.3390%2fvaccines10081268&partnerID=40&md5=41ca03edc64237f2b80e568f3c3922b8
dc.subjectad26.cov2.s vaccineen
dc.subjectnovokininen
dc.subjectsynthetic peptideen
dc.subjecttozinameranen
dc.subjectunclassified drugen
dc.subjectvaxzevriaen
dc.subjectalternative medicineen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectantibody responseen
dc.subjectantibody titeren
dc.subjectantiinflammatory activityen
dc.subjectantioxidant activityen
dc.subjectarticleen
dc.subjectArticleen
dc.subjectbinding affinityen
dc.subjectchemoluminescenceen
dc.subjectcolumn chromatographyen
dc.subjectdrug efficacyen
dc.subjectdrug metabolismen
dc.subjectdrug therapyen
dc.subjectenzyme linked immunosorbent assayen
dc.subjectfood frequency questionnaireen
dc.subjectgene expressionen
dc.subjecthigh performance liquid chromatographyen
dc.subjecthumoral immunityen
dc.subjectimmunogenicityen
dc.subjectlimit of quantitationen
dc.subjectliquid chromatographyen
dc.subjectliquid chromatography-mass spectrometryen
dc.subjectlow drug doseen
dc.subjectmass spectrometryen
dc.subjectmorbidityen
dc.subjectmouseen
dc.subjectmultiple reaction monitoringen
dc.subjectMycobacterium butyricumen
dc.subjectneurite outgrowthen
dc.subjectnonhumanen
dc.subjectparticle sizeen
dc.subjectpeptide synthesisen
dc.subjectphytochemistryen
dc.subjectprotein expressionen
dc.subjectprotein purificationen
dc.subjectpublic healthen
dc.subjectrheumatoid arthritisen
dc.subjectscoring systemen
dc.subjectSevere acute respiratory syndrome coronavirus 2en
dc.subjectspikeen
dc.subjectsustained drug releaseen
dc.subjectvaccinationen
dc.subjectWestern blottingen
dc.subjectMDPIen
dc.titleIntensity of Humoral Immune Responses, Adverse Reactions, and Post-Vaccination Morbidity after Adenovirus Vector-Based and mRNA Anti-COVID-19 Vaccinesen
dc.typejournalArticleen


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