The clinical application of cancer immunotherapy based on naturally circulating dendritic cells.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
18 04 2019
Historique:
received: 11 02 2019
accepted: 26 03 2019
entrez: 20 4 2019
pubmed: 20 4 2019
medline: 8 7 2020
Statut: epublish

Résumé

Dendritic 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

Identifiants

pubmed: 30999964
doi: 10.1186/s40425-019-0580-6
pii: 10.1186/s40425-019-0580-6
pmc: PMC6471787
doi:

Substances chimiques

Antigens, CD1 0
CD1C protein, human 0
Cancer Vaccines 0
Glycoproteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

109

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Auteurs

Kalijn F Bol (KF)

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
Department of Medical Oncology, Radboud university medical centre, Nijmegen, the Netherlands.

Gerty Schreibelt (G)

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.

Katrin Rabold (K)

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
Radiotherapy & OncoImmunology Laboratory, Radboud university medical centre, Nijmegen, the Netherlands.

Stefanie K Wculek (SK)

Immunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares `Carlos III`, Madrid, Spain.

Julia Katharina Schwarze (JK)

Department of Medical Oncology, Universitair Ziekenhuis Brussel, Brussels, Belgium.

Andrzej Dzionek (A)

Miltenyi Biotec GmbH, Bergisch-Gladbach, Germany.

Alvaro Teijeira (A)

Center for Applied Medical Research, University of Navarra, Pamplona, Spain.

Lana E Kandalaft (LE)

Department of Oncology, Lausanne University Hospital, Lausanne, Switzerland.

Pedro Romero (P)

Department of Oncology, Lausanne University Hospital, Lausanne, Switzerland.

George Coukos (G)

Department of Oncology, Lausanne University Hospital, Lausanne, Switzerland.

Bart Neyns (B)

Department of Medical Oncology, Universitair Ziekenhuis Brussel, Brussels, Belgium.

David Sancho (D)

Immunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares `Carlos III`, Madrid, Spain.

Ignacio Melero (I)

Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
CIBERONC, Madrid, Spain.

I Jolanda M de Vries (IJM)

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands. Jolanda.deVries@radboudumc.nl.
Department of Medical Oncology, Radboud university medical centre, Nijmegen, the Netherlands. Jolanda.deVries@radboudumc.nl.

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