Show simple item record

dc.contributor.authorMartin-Vicente, Maria 
dc.contributor.authorCarrasco, Itziar
dc.contributor.authorMuñoz-Gómez, María José 
dc.contributor.authorHernanz Lobo, Alicia
dc.contributor.authorMas-Lloret, Vicente 
dc.contributor.authorVigil-Vázquez, Sara
dc.contributor.authorVazquez-Alcaraz, Monica 
dc.contributor.authorManzanares, Angela
dc.contributor.authorCano, Olga 
dc.contributor.authorAlonso, Roberto
dc.contributor.authorSepulveda-Crespo, Daniel 
dc.contributor.authorTarancon-Diez, Laura
dc.contributor.authorMuñoz-Fernández, María Ángeles
dc.contributor.authorMuñoz-Chapuli, Mar
dc.contributor.authorResino, Salvador 
dc.contributor.authorNavarro, Maria Luisa
dc.contributor.authorMartinez, Isidoro 
dc.date.accessioned2024-02-06T08:00:18Z
dc.date.available2024-02-06T08:00:18Z
dc.date.issued2023-06
dc.identifier.citationBirth. 2023 Jun;50(2):418-427.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17491
dc.description.abstractIntroduction: Pregnant women are vulnerable to severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection. Neutralizing antibodies against the SARS-CoV-2 spike (S) protein protect from severe disease. This study analyzes the antibody titers to SARS-CoV-2 S protein in pregnant women and their newborns at delivery, and six months later. Methods: We conducted a prospective study on pregnant women with confirmed SARS-CoV-2 infection and newborns. Antibody (IgG, IgM, and IgA) titers were determined using immunoassays in serum and milk samples. An angiotensin-converting enzyme 2 (ACE2) receptor-binding inhibition assay to the S protein was performed on the same serum and milk samples. Results: At birth, antibodies to SARS-CoV-2 spike protein were detected in 81.9% of mothers' sera, 78.9% of cord blood samples, and 63.2% of milk samples. Symptomatic women had higher antibody titers (IgG, IgM, and IgA) than the asymptomatic ones (P < 0.05). At six months postpartum, IgG levels decreased drastically in children's serum (P < 0.001) but remained high in mothers' serum. Antibody titers correlated positively with its capacity to inhibit the ACE2-spike protein interaction at baseline in maternal sera (R2 = 0.203; P < 0.001), cord sera (R2 = 0.378; P < 0.001), and milk (R2 = 0.564; P < 0.001), and at six months in maternal sera (R2 = 0.600; P < 0.001). Conclusions: High antibody levels against SARS-CoV-2 spike protein were found in most pregnant women. Due to the efficient transfer of IgG to cord blood and high IgA titers in breast milk, neonates may be passively immunized to SARS-CoV-2 infection. Our findings could guide newborn management and maternal vaccination policies.es_ES
dc.description.sponsorshipThis study was supported by grants from Instituto de Salud Carlos III (ISCII; grant numbers COV20_00808). The study was also funded by the Centro de Investigación Biomédica en Red (CIBER) de Enfermedades Infecciosas (CB21/13/00044 and CB21/13/00077). DSC is a “Sara Borrell” researcher from ISCIII (grant number CD20CIII/00001) and has been supported by a fellowship award from Fundación ONCE “Oportunidad al Talento”.es_ES
dc.language.isoenges_ES
dc.publisherWiley es_ES
dc.type.hasVersionSMURes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntibodyes_ES
dc.subjectBreast milkes_ES
dc.subjectCord bloodes_ES
dc.subjectNewbornes_ES
dc.subjectPregnantes_ES
dc.subjectSARS-CoV-2es_ES
dc.subjectSpike glycoproteines_ES
dc.subject.meshCOVID-19es_ES
dc.subject.meshPregnancy Complications, Infectious es_ES
dc.subject.meshInfant, Newborn es_ES
dc.subject.meshPregnancy es_ES
dc.subject.meshFemale es_ES
dc.subject.meshChild es_ES
dc.subject.meshHumans es_ES
dc.subject.meshMothers es_ES
dc.subject.meshSpike Glycoprotein, Coronaviruses_ES
dc.subject.meshAngiotensin-Converting Enzyme 2es_ES
dc.subject.meshProspective Studies es_ES
dc.subject.meshSARS-CoV-2es_ES
dc.subject.meshImmunoglobulin A es_ES
dc.subject.meshImmunoglobulin G es_ES
dc.subject.meshImmunoglobulin M es_ES
dc.titleAntibody levels to SARS-CoV-2 spike protein in mothers and children from delivery to six months lateres_ES
dc.typeresearch articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID35802776es_ES
dc.format.volume50es_ES
dc.format.number2es_ES
dc.format.page418-427es_ES
dc.identifier.doi10.1111/birt.12667es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas) es_ES
dc.contributor.funderFundación ONCE es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1523-536Xes_ES
dc.relation.publisherversionhttps://doi.org/10.1111/birt.12667es_ES
dc.identifier.journalBirth (Berkeley, Calif.)es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/COV20/00808es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB21/13/00044es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB21/13/00077es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CD20CIII/00001es_ES


Files in this item

Acceso Abierto
Thumbnail

This item appears in the following Collection(s)

Show simple item record

Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This item is licensed under a: Attribution-NonCommercial-NoDerivatives 4.0 Internacional