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In vitro neutralizing activity of BNT162b2 mRNA-induced antibodies against full B.1.351 SARS-CoV-2 variant.

dc.contributor.authorSerrano-Conde, Esther
dc.contributor.authorLeyva, Alba
dc.contributor.authorFuentes, Ana
dc.contributor.authorde Salazar, Adolfo
dc.contributor.authorChueca, Natalia
dc.contributor.authorPerez-Castro, Sonia
dc.contributor.authorRegueiro, Benito
dc.contributor.authorRojas, Almudena
dc.contributor.authorMendoza, Joaquin
dc.contributor.authorRojas, Jose
dc.contributor.authorGarcia, Federico
dc.date.accessioned2023-05-03T13:29:41Z
dc.date.available2023-05-03T13:29:41Z
dc.date.issued2021-12-08
dc.description.abstractSARS-CoV-2 variation represents a serious challenge to current COVID-19 vaccines. Recent reports suggest that B.1.351 and other variants may escape the neutralization activity of the antibodies generated by current vaccines. Ninety-nine healthcare workers undertaking BNT162b2 mRNA vaccination were sampled at baseline, on the day of the second dose, and 14 days after the latter. Neutralization activity against SARS-CoV-2 B.1, B.1.1.7 and B.1.351 was investigated using a Vero-E6 model. Eleven of the study participants had prior infection with SARS-CoV-2. Neutralization titers against the B.1 and the B.1.1.7 variants were not statistically different and were significantly higher than titers against the B.1.351 variant across pre-exposed and non-pre-exposed vaccinated individuals (p 1/80 after a single dose, while only 11% of non-exposed vaccinated individuals had titers >1/80. BNT162b2 mRNA-induced antibodies show a lower in vitro neutralizing activity against B.1.351 variant compared to neutralization against B.1.1.7 or B.1 variants. Interestingly, for individuals pre-exposed to SARS-CoV-2, one dose of BNT162b2 mRNA may be adequate to produce neutralizing antibodies against B.1.1.7 and B.1, while two doses of BNT162b2 mRNA provide optimal neutralizing antibody response against B.1.351 too.
dc.description.versionSi
dc.identifier.citationSerrano-Conde E, Leyva A, Fuentes A, de Salazar A, Chueca N, Pérez-Castro S, et al. In vitro neutralizing activity of BNT162b2 mRNA-induced antibodies against full B.1.351 SARS-CoV-2 variant. Transbound Emerg Dis. 2022 Sep;69(5):2649-2655.
dc.identifier.doi10.1111/tbed.14417
dc.identifier.essn1865-1682
dc.identifier.pmid34910373
dc.identifier.unpaywallURLhttps://doi.org/10.22541/au.163881397.76967489/v1
dc.identifier.urihttp://hdl.handle.net/10668/20020
dc.issue.number5
dc.journal.titleTransboundary and emerging diseases
dc.journal.titleabbreviationTransbound Emerg Dis
dc.language.isoen
dc.organizationHospital Universitario San Cecilio
dc.organizationInstituto de Investigación Biosanitaria de Granada (ibs.GRANADA)
dc.page.number2
dc.provenanceRealizada la curación de contenido 18/07/2024
dc.publisherHindawi Limited
dc.pubmedtypeJournal Article
dc.relation.publisherversionhttps://doi.org/10.1111/tbed.14417
dc.rights.accessRightsRestricted Access
dc.subjectB.1
dc.subjectB.1.1.7
dc.subjectB.1.351
dc.subjectBNT162b2 mRNA
dc.subjectSARS-CoV-2
dc.subjectneutralization
dc.subjectvariants
dc.subject.decsARN Mensajero
dc.subject.decsAnimales
dc.subject.decsAnticuerpos antivirales
dc.subject.decsAnticuerpos neutralizantes
dc.subject.decsGlicoproteína de la espiga del coronavirus
dc.subject.decsGlicoproteínas de membrana Humanos
dc.subject.decsProteínas del envoltorio viral
dc.subject.decsPruebas de neutralización
dc.subject.decsSARS-CoV-2
dc.subject.decsVacuna BNT162
dc.subject.decsVacunas contra la COVID-19
dc.subject.meshAnimals
dc.subject.meshAntibodies, Neutralizing
dc.subject.meshAntibodies, Viral
dc.subject.meshBNT162 Vaccine
dc.subject.meshCOVID-19
dc.subject.meshCOVID-19 Vaccines
dc.subject.meshHumans
dc.subject.meshMembrane Glycoproteins
dc.subject.meshNeutralization Tests
dc.subject.meshRNA, Messenger
dc.subject.meshSARS-CoV-2
dc.subject.meshSpike Glycoprotein, Coronavirus
dc.subject.meshViral Envelope Proteins
dc.titleIn vitro neutralizing activity of BNT162b2 mRNA-induced antibodies against full B.1.351 SARS-CoV-2 variant.
dc.typeresearch article
dc.type.hasVersionSMUR
dc.volume.number69
dspace.entity.typePublication

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