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Authordc.contributor.authorClavero, René
Authordc.contributor.authorParra Lucares, Alfredo Andrés
Authordc.contributor.authorMéndez Valdés, Gabriel Andrés
Authordc.contributor.authorVilla, Eduardo
Authordc.contributor.authorBravo Espinoza, Karin Constanza
Authordc.contributor.authorMondaca, Evelyn
Authordc.contributor.authorAranda, Josseline
Authordc.contributor.authorBrignardello, Rose
Authordc.contributor.authorGajardo, Cynthia
Authordc.contributor.authorOrdenes, Angélica
Authordc.contributor.authorColombo, Evelyn
Authordc.contributor.authorTapia, Jessica
Authordc.contributor.authorEtcheverry, Andoni
Authordc.contributor.authorZúñiga, José
Authordc.contributor.authorToro Cabrera, Luis Alejandro
Admission datedc.date.accessioned2023-07-18T18:35:35Z
Available datedc.date.available2023-07-18T18:35:35Z
Publication datedc.date.issued2022
Cita de ítemdc.identifier.citationVaccines 2022, 10, 1542es_ES
Identifierdc.identifier.other10.3390/vaccines10091542
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/194807
Abstractdc.description.abstractThe CoronaVac vaccine is the most used anti-SARS-CoV-2 vaccine worldwide. Previous data indicate that this vaccine produces a lower immune response than RNA vaccines such as BNT162b2. End-stage renal disease (ESRD) patients have an increased rate of COVID-19 and a reduced immune response to vaccinations. Currently, there is little data on this population's immune response induced by CoronaVac. Methods: This study involved a prospective cohort of ESRD patients in chronic hemodialysis who received a two-dose immunization scheme of either CoronaVac (Sinovac Biotech) or BNT162b2 vaccines (Pfizer-BioNTech). We measured the plasma levels of anti-SARS-CoV-2 IgG antibodies. We determined antibody titers before immunization, 2 and 4 months after two doses, plus 4 months after a booster dose. Results: We evaluated 208 patients in three hemodialysis centers. The mean age was 62.6 +/- 15.6 years, of whom 91 were female (41.75%). Eighty-one patients (38.94%) received the BNT162b2 vaccine and 127 (61.06%) received the CoronaVac vaccine. Patients who received the BNT162b2 vaccine had a higher humoral response compared to those who received the CoronaVac vaccine (4 months after the second dose: BNT162b2: 88.89%, CoronaVac: 51.97%, p < 0.001; 4 months after the booster: BNT162b2: 98.77%, CoronaVac: 86.61%, p < 0.001). Conclusions: Our results suggest that the CoronaVac vaccine induced a lower humoral response than the BNT162b2 vaccine in ESRD patients on hemodialysis.es_ES
Patrocinadordc.description.sponsorshipFONDECYT Regular of the Agencia Nacional de Investigacion y Desarrollo (ANID) 1221571es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherMDPIes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceVaccineses_ES
Keywordsdc.subjectRenal dialysises_ES
Keywordsdc.subjectHemodialysises_ES
Keywordsdc.subjectSARS-CoV-2es_ES
Keywordsdc.subjectImmune responseantibodyes_ES
Keywordsdc.subjectCOVID-19 (Enfermedad)es_ES
Keywordsdc.subjectCOVID-19-UCHes_ES
Títulodc.titleHumoral immune response of BNT162b2 and CoronaVac vaccinations in hemodialysis patients: a multicenter prospective cohortes_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publícación WoSes_ES


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States