Publication:
Persistent Immunity against SARS-CoV-2 in Individuals with Oncohematological Diseases Who Underwent Autologous or Allogeneic Stem Cell Transplantation after Vaccination

dc.contributor.authorRodríguez-Mora, Sara
dc.contributor.authorPérez-Lamas, Lucía
dc.contributor.authorSainero, Miriam Solera
dc.contributor.authorTorres, Montserrat
dc.contributor.authorSánchez-Menéndez, Clara
dc.contributor.authorCorona, Magdalena
dc.contributor.authorMateos, Elena
dc.contributor.authorCasado-Fernández, Guiomar
dc.contributor.authorAlcamí, José
dc.contributor.authorGarcía-Pérez, Javier
dc.contributor.authorPerez-Olmeda, Mayte
dc.contributor.authorMurciano-Antón, María Aranzazu
dc.contributor.authorLópez-Jiménez, Javier
dc.contributor.authorGarcía-Gutiérrez, Valentín
dc.contributor.authorCoiras, Mayte
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderNational Institutes of Health (Estados Unidos)
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas)
dc.contributor.funderInstituto Ramón y Cajal de Investigación Sanitaria (España)es_ES
dc.date.accessioned2023-05-11T08:13:29Z
dc.date.available2023-05-11T08:13:29Z
dc.date.issued2023-02
dc.description.abstractThe high morbimortality due to SARS-CoV-2 infection in oncohematological diseases (OHD) and hematopoietic stem cell transplant (HSCT) recipients in the pre-vaccine era has made vaccination a priority in this group. After HSCT, the immune responses against common vaccines such as tetanus, varicella, rubella, and polio may be lost. However, the loss of immunity developed by COVID-19 vaccination after HSCT has not been completely defined. In this study, both humoral and cellular immunity against SARS-CoV-2 were analyzed in 29 individuals with OHD who were vaccinated before receiving allogeneic (n = 11) or autologous (n = 18) HSCT. All participants had low but protective levels of neutralizing IgGs against SARS-CoV-2 after HSCT despite B-cell lymphopenia and immaturity. Although antibody-dependent cellular cytotoxicity was impaired, direct cellular cytotoxicity was similar to healthy donors in participants with autologous-HSCT, in contrast to individuals with allogeneic–HSCT, which severely deteriorated. No significant changes were observed in the immune response before and after HSCT. During follow-up, all reported post-HSCT SARS-CoV-2 infections were mild. This data emphasizes that COVID-19 vaccination is effective, necessary, and safe for individuals with OHD and also supports the persistence of some degree of immune protection after HSCT, at least in the short term, when patients cannot yet be revaccinated.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by projects PI21/00877 and PI22CIII/00059, funded by the Strategic Action in Health of the Instituto de Salud Carlos III (SICIII) and co-funded by European Regional Development Fund (ERDF), “A way to make Europe”; the Coordinated Research Activities at the National Center of Microbiology (CNM, Instituto de Salud Carlos III) (COV20_00679) to promote an integrated response against SARS-CoV-2 in Spain (Spanish Ministry of Science and Innovation) that is coordinated by Dr Inmaculada Casas (WHO National Influenza Center of the CNM); a generous donation provided by Chiesi España, S.A.U. (Barcelona, Spain); and the Spanish Ministry of Science and Innovation (PID2019-110275RB-I00). The work of Sara Rodríguez-Mora is financed by NIH grant R01AI143567. The work of Montserrat Torres and Guiomar Casado are financed by CIBERINFEC, co-financed by ERDF, “A way to make Europe”. The work of Clara Sánchez-Menéndez is financed by Programa Investigo, FIBio HRC-IRYCIS, co-financed by ERDF, “A way to make Europe”.es_ES
dc.format.page2344es_ES
dc.format.volume15es_ES
dc.identifier.citationCancers. 2023,15:2344.es_ES
dc.identifier.doi10.3390/cancers15082344es_ES
dc.identifier.e-issn2072-6694es_ES
dc.identifier.journalCancerses_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16050
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2019-110275RB-I00es_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III///PI21 - Proyectos de investigacion en salud (AES 2021). Modalidad proyectos de investigación en salud. (2021)/PI21/00877es_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III///PI22-ISCIII Proyectos de I+D+I en salud (AES 2022).Intramurales (2022)/PI22CIII/00059es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/COV20_00679es_ES
dc.relation.publisherversionhttps://doi.org/10.3390/cancers15082344es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCOVID-19 vaccinees_ES
dc.subjectAutologous transplantationes_ES
dc.subjectAllogeneic transplantationes_ES
dc.subjectCytotoxic responsees_ES
dc.subjectHumoral responsees_ES
dc.titlePersistent Immunity against SARS-CoV-2 in Individuals with Oncohematological Diseases Who Underwent Autologous or Allogeneic Stem Cell Transplantation after Vaccinationes_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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