Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/40141
Title: Seroconversion rate after primary vaccination with two doses of BNT162b2 versus mRNA-1273 in solid organ transplant recipients: a systematic review and meta-analysis
Authors: Verleye, Arno
Wijtvliet, Veerle
ABRAMS, Steven 
Hellemans, Rachel
Bougrea, Rania
Massart, Annick
Pipeleers, Lissa
Wissing, Karl Martin
Ariën, Kevin K
De Winter, Benedicte Y
Van Damme, Pierre
Abramowicz, Daniel
Ledeganck, Kristien J
Issue Date: 2022
Publisher: 
Source: Nephrology, dialysis, transplantation, 37 (8) , p. 1566 -1575
Abstract: Background.Inthegeneralpopulation,theseroconversion rateafterprimaryvaccinationwithtwodosesofanantisevereacuterespiratorysyndromecoronavirus2messenger RNA(mRNA)vaccinereachesnearly100%,withsignificantly higherantibodytitersaftermRNA-1273vaccinationcompared toBNT162b2vaccination.Hereweperformedasystematic reviewandmeta-analysistocomparetheantibodyresponse aftertwo-dosemRNA-1273versusBNT162b2vaccinationin solidorgantransplant(SOT)recipients. Methods.Asystematicliteraturereviewwasperformedusing PubMed,WebofScienceandtheCochraneLibraryand originalresearchpaperswereincludedforameta-analysisto calculatevaccine-specificseroconversionratesforeachofthe mRNAvaccines.Next,thepooledrelativeseroconversionrate wasestimated. Results.Eightstudiesthatdescribedthedevelopmentofantibodiesagainstreceptor-bindingdomain(RBD)and/orspike proteinwereeligibleformeta-analysis.Twoofthesestudies alsoreportedantibodytiters.Themeta-analysisrevealedlower seroconversionratesinSOTrecipientsvaccinatedwithtwo dosesofBNT162b2{44.3%[95%confidenceinterval(CI) 34.1–54.7]}ascomparedwithpatientsvaccinatedwithtwo dosesofmRNA-1273[58.4%(95%CI47.2–69.2)].Therelative seroconversionratewas0.795(95%CI0.732–0.864). Conclusions.Thissystematicreviewandmeta-analysis indicatesthatinSOTrecipients,higherseroconversionrates wereobservedaftervaccinationwithmRNA-1273compared withBNT162b2.
Document URI: http://hdl.handle.net/1942/40141
ISSN: 0931-0509
e-ISSN: 1460-2385
DOI: 10.1093/ndt/gfac174
Rights: The Author(s) 2022.Published by Oxford University Presson behalf of the ERA. Allrights reserved. For permissions, please e-mail: journals.permissions@oup.com. Free access
Category: A1
Type: Journal Contribution
Validations: vabb 2024
Appears in Collections:Research publications

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