Publication:
Is It Feasible to Use CMV-Specific T-Cell Adoptive Transfer as Treatment Against Infection in SOT Recipients?

dc.contributor.authorGarcia-Rios, Estefani
dc.contributor.authorNuévalos, Marcos
dc.contributor.authorMancebo, Francisco Jose
dc.contributor.authorPerez-Romero, Pilar
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)es_ES
dc.contributor.funderRETICS-Investigación en Patología Infecciosa (REIPI-ISCIII) (España)es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.date.accessioned2021-12-03T13:39:03Z
dc.date.available2021-12-03T13:39:03Z
dc.date.issued2021-04-23
dc.description.abstractDuring the last decade, many studies have demonstrated the role of CMV specific T-cell immune response on controlling CMV replication and dissemination. In fact, it is well established that transplanted patients lacking CMV-specific T-cell immunity have an increased occurrence of CMV replication episodes and CMV-related complications. In this context, the use of adoptive transfer of CMV-specific T-cells has been widely investigated and applied to Hematopoietic Stem Cell Transplant patients and may be useful as a therapeutic alternative, to reconstitute the CMV specific T-cell response and to control CMV viremia in patients receiving a transplantation. However, only few authors have explored the use of T-cell adoptive transfer in SOT recipients. We propose a novel review in which we provide an overview of the impact of using CMV-specific T-cell adoptive transfer on the control of CMV infection in SOT recipients, the different approaches to stimulate, isolate and expand CMV-specific T-cells developed over the years and a discussion of the possible use of CMV adoptive cellular therapy in this SOT population. Given the timeliness and importance of this topic, we believe that such an analysis will provide important insights into CMV infection and its treatment/prevention.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis study was supported by the Spanish Ministry of Science, Innovation and University, Instituto de Salud Carlos III Grant/Award Numbers: PI17CIII-00014 (MPY110/18); DTS18CIII/00006 (MPY127/19); PI20-009 (MPY303/20). This work was supported by Plan Nacional de I + D+i 2013‐2016 and Instituto de Salud Carlos III, Subdirección General de Redes y Centros de Investigación Cooperativa, Ministry of Science, Innovation and University, Spanish Network for Research in Infectious Diseases (REIPI RD16/0016/0009), co-financed by European Development Regional Fund ‘A way to achieve Europe’. EG-R is supported by the Sara Borrell Program (CD18CIII/00007), Instituto de Salud Carlos III, Ministerio de Ciencia, Innovación y Universidades. FM is supported by the PFIS Program (F18III/00013), Instituto de Salud Carlos III, Ministerio de Ciencia, Innovación y Universidades. MN is supported by the FPU program (FPU19/05927), Ministerio de Ciencia, Innovación y Universidades.es_ES
dc.format.page657144es_ES
dc.format.volume12es_ES
dc.identifier.citationFront. Immunol. 2021 Apr 23;12:657144.es_ES
dc.identifier.doi10.3389/fimmu.2021.657144es_ES
dc.identifier.e-issn1664-3224es_ES
dc.identifier.journalFrontiers In Immunologyes_ES
dc.identifier.pubmedID33968058es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/13483
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/MPY110/18es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/MPY127/19es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/MPY303/20es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0016/0009es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CD18CIII/00007es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/F18III/00013es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/FPU19/05927es_ES
dc.relation.publisherversionhttps://doi.org/10.3389/fimmu.2021.657144es_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.subjectCMV treatmentes_ES
dc.subjectCMV-specific immune responsees_ES
dc.subjectT-cell adoptive transferes_ES
dc.subjectCellular therapyes_ES
dc.subjectCytomegaloviruses_ES
dc.subject.meshAdoptive Transferes_ES
dc.subject.meshCytokineses_ES
dc.subject.meshCytomegaloviruses_ES
dc.subject.meshCytomegalovirus Infectionses_ES
dc.subject.meshDisease Managementes_ES
dc.subject.meshDisease Susceptibilityes_ES
dc.subject.meshHumanses_ES
dc.subject.meshImmunotherapy, Adoptivees_ES
dc.subject.meshOrgan Transplantationes_ES
dc.subject.meshT-Cell Antigen Receptor Specificityes_ES
dc.subject.meshT-Lymphocyteses_ES
dc.subject.meshTreatment Outcomees_ES
dc.titleIs It Feasible to Use CMV-Specific T-Cell Adoptive Transfer as Treatment Against Infection in SOT Recipients?es_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication50b540df-28b6-4182-a1ee-d7ee50b0114e
relation.isAuthorOfPublicationa8701781-127b-4e2f-af69-7b47489dafb3
relation.isAuthorOfPublication619c44d6-0adf-4ccf-9b6a-66663bad5429
relation.isAuthorOfPublication.latestForDiscovery50b540df-28b6-4182-a1ee-d7ee50b0114e

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