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The current status of mesenchymal stromal cells: controversies, unresolved issues and some promising solutions to improve their therapeutic efficacy

dc.contributor.authorGarcía Bernal, David
dc.contributor.authorGarcía Arranz, Mariano
dc.contributor.authorYáñez, Rosa
dc.contributor.authorHervás Salcedo, Rosario
dc.contributor.authorCortés Rubio, José Alfonso
dc.contributor.authorFernández García, María
dc.contributor.authorHernando Rodríguez, Miriam
dc.contributor.authorQuintana Bustamante, Óscar
dc.contributor.authorBueren, Juan A.
dc.contributor.authorGarcía Olmo, Damián
dc.contributor.authorMoraleda, Jose María
dc.contributor.authorSegovia, Jose Carlos
dc.contributor.authorZapata González, Agustín
dc.date.accessioned2023-06-17T09:15:58Z
dc.date.available2023-06-17T09:15:58Z
dc.date.issued2021-03-16
dc.description.abstractMesenchymal stromal cells (MSCs) currently constitute the most frequently used cell type in advanced therapies with different purposes, most of which are related with inflammatory processes. Although the therapeutic efficacy of these cells has been clearly demonstrated in different disease animal models and in numerous human phase I/II clinical trials, only very few phase III trials using MSCs have demonstrated the expected potential therapeutic benefit. On the other hand, diverse controversial issues on the biology and clinical applications of MSCs, including their specific phenotype, the requirement of an inflammatory environment to induce immunosuppression, the relevance of the cell dose and their administration schedule, the cell delivery route (intravascular/systemic vs. local cell delivery), and the selected cell product (i.e., use of autologous vs. allogeneic MSCs, freshly cultured vs. frozen and thawed MSCs, MSCs vs. MSC-derived extracellular vesicles, etc.) persist. In the current review article, we have addressed these issues with special emphasis in the new approaches to improve the properties and functional capabilities of MSCs after distinct cell bioengineering strategies.en
dc.description.departmentDepto. de Biología Celular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII)/Fondo Europeo de Desarrollo Regional
dc.description.sponsorshipComunidad de Madrid
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/68226
dc.identifier.citationGarcía-Bernal D, García-Arranz M, Yáñez RM, Hervás-Salcedo R, Cortés A, Fernández-García M, et al. The Current Status of Mesenchymal Stromal Cells: Controversies, Unresolved Issues and Some Promising Solutions to Improve Their Therapeutic Efficacy. Front Cell Dev Biol 2021;9:650664. https://doi.org/10.3389/fcell.2021.650664.
dc.identifier.doi10.3389/fcell.2021.650664
dc.identifier.essn2296-634X
dc.identifier.officialurlhttps//doi.org/10.3389/fcell.2021.650664
dc.identifier.relatedurlhttps://www.frontiersin.org/articles/10.3389/fcell.2021.650664/full
dc.identifier.urihttps://hdl.handle.net/20.500.14352/8502
dc.issue.number650664
dc.journal.titleFrontiers in Cell and Developmental Biology
dc.language.isoeng
dc.page.final18
dc.page.initial1
dc.publisherFrontiers Media
dc.relation.projectID(RTI2018-093938-B-I00)
dc.relation.projectID(RD16/0011/0001, RD16/0011/0002, RD16/0011/0011, and RD16/0011/0013)
dc.relation.projectIDAvancell-CM (S2017/BMD-3692)
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu576.3
dc.subject.cdu615.361.018.1
dc.subject.keywordMSC bioengineering
dc.subject.keywordMSC homing
dc.subject.keywordMSC immunomodulation
dc.subject.keywordMSC preconditioning
dc.subject.keywordMSC therapeutic efficacy
dc.subject.ucmBiología celular (Biología)
dc.subject.unesco2407 Biología Celular
dc.titleThe current status of mesenchymal stromal cells: controversies, unresolved issues and some promising solutions to improve their therapeutic efficacyen
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
relation.isAuthorOfPublicationfd0e8629-0146-46ce-9ba3-4e4d7e6239da
relation.isAuthorOfPublication.latestForDiscoveryfd0e8629-0146-46ce-9ba3-4e4d7e6239da

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