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dc.creatorCoukos, G. (George)-
dc.creatorVries, J. (Jolanda) de-
dc.creatorMelero, I. (Ignacio)-
dc.creatorSancho, D. (David)-
dc.creatorNeyns, B. (Bart)-
dc.creatorBol, K.F. (Kalijn F.)-
dc.creatorSchreibelt, G. (Gerty)-
dc.creatorRabold, K. (Katrin)-
dc.creatorWculek, S.K. (Stefanie K.)-
dc.creatorSchwarze, J.K. (Julia Katharina)-
dc.creatorDzionek, A. (Andrzej)-
dc.creatorTeijeira, A. (Álvaro)-
dc.creatorKandalaft, L.E. (Lana E.)-
dc.creatorRomero, P.J. (Pedro J.)-
dc.date.accessioned2021-11-10T13:33:56Z-
dc.date.available2021-11-10T13:33:56Z-
dc.date.issued2019-
dc.identifier.citationBol, K.F. (Kalijn F.); Schreibelt, G. (Gerty); Rabold, K. (Katrin); et al. "The clinical application of cancer immunotherapy based on naturally circulating dendritic cells". Journal for ImmunoTherapy of Cancer. 7 (1), 2019, 109es_ES
dc.identifier.issn2051-1426-
dc.identifier.urihttps://hdl.handle.net/10171/62525-
dc.description.abstractDendritic cells (DCs) can initiate and direct adaptive immune responses. This ability is exploitable in DC vaccination strategies, in which DCs are educated ex vivo to present tumor antigens and are administered into the patient with the aim to induce a tumor-specific immune response. DC vaccination remains a promising approach with the potential to further improve cancer immunotherapy with little or no evidence of treatment-limiting toxicity. However, evidence for objective clinical antitumor activity of DC vaccination is currently limited, hampering the clinical implementation. One possible explanation for this is that the most commonly used monocyte-derived DCs may not be the best source for DC-based immunotherapy. The novel approach to use naturally circulating DCs may be an attractive alternative. In contrast to monocyte-derived DCs, naturally circulating DCs are relatively scarce but do not require extensive culture periods. Thereby, their functional capabilities are preserved, the reproducibility of clinical applications is increased, and the cells are not dysfunctional before injection. In human blood, at least three DC subsets can be distinguished, plasmacytoid DCs, CD141+ and CD1c+ myeloid/conventional DCs, each with distinct functional characteristics. In completed clinical trials, either CD1c+ myeloid DCs or plasmacytoid DCs were administered and showed encouraging immunological and clinical outcomes. Currently, also the combination of CD1c+ myeloid and plasmacytoid DCs as well as the intratumoral use of CD1c+ myeloid DCs is under investigation in the clinic. Isolation and culture strategies for CD141+ myeloid DCs are being developed. Here, we summarize and discuss recent clinical developments and future prospects of natural DC-based immunotherapy.es_ES
dc.description.sponsorshipThis work was supported by EU grant PROCROP (635122).es_ES
dc.language.isospaes_ES
dc.publisherBMJes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/635122/EU-
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectPlasmacytoid dendritic cellses_ES
dc.subjectVaccinationes_ES
dc.subjectImmunotherapyes_ES
dc.subjectCanceres_ES
dc.subjectCross-presenting dendritic cellses_ES
dc.subjectConventional dendritic cellses_ES
dc.subjectMyeloid dendritic cellses_ES
dc.subjectDendritic cellses_ES
dc.subjectNatural dendritic cellses_ES
dc.titleThe clinical application of cancer immunotherapy based on naturally circulating dendritic cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.description.noteThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.es_ES
dc.identifier.doi10.1186/s40425-019-0580-6-
dadun.citation.number1es_ES
dadun.citation.publicationNameJournal for ImmunoTherapy of Canceres_ES
dadun.citation.startingPage109es_ES
dadun.citation.volume7es_ES

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