Quantitative and qualitative impairments in dendritic cell subsets of patients with ovarian or prostate cancer.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
08 2020
Historique:
received: 20 03 2020
accepted: 16 04 2020
pubmed: 27 6 2020
medline: 31 12 2020
entrez: 27 6 2020
Statut: ppublish

Résumé

Dendritic cells (DCs) are the most efficient antigen-presenting cells, hence initiating a potent and cancer-specific immune response. This ability (mainly using monocyte-derived DCs) has been exploited in vaccination strategies for decades with limited clinical efficacy. Another alternative would be the use of conventional DCs (cDCs) of which at least three subsets circulate in human blood: cDC1s (CD141 Whole blood samples from patients with OvC or PrC and healthy donors (HDs) were evaluated by flow cytometry for the phenotypic and functional characterisation of DC subsets. In both patient groups, the frequency of total CD141 cDC1s are reduced in patients with OvC, and CD141

Sections du résumé

BACKGROUND
Dendritic cells (DCs) are the most efficient antigen-presenting cells, hence initiating a potent and cancer-specific immune response. This ability (mainly using monocyte-derived DCs) has been exploited in vaccination strategies for decades with limited clinical efficacy. Another alternative would be the use of conventional DCs (cDCs) of which at least three subsets circulate in human blood: cDC1s (CD141
PATIENTS AND METHODS
Whole blood samples from patients with OvC or PrC and healthy donors (HDs) were evaluated by flow cytometry for the phenotypic and functional characterisation of DC subsets.
RESULTS
In both patient groups, the frequency of total CD141
CONCLUSIONS
cDC1s are reduced in patients with OvC, and CD141

Identifiants

pubmed: 32590296
pii: S0959-8049(20)30240-9
doi: 10.1016/j.ejca.2020.04.036
pii:
doi:

Substances chimiques

Antigens, Surface 0
CA-125 Antigen 0
CLEC9a protein, human 0
Lectins, C-Type 0
MUC16 protein, human 0
Membrane Proteins 0
Receptors, Mitogen 0
THBD protein, human 0
TLR3 protein, human 0
Thrombomodulin 0
Toll-Like Receptor 3 0
Poly I-C O84C90HH2L

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

173-182

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement None declared.

Auteurs

Beatris Mastelic-Gavillet (B)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Apostolos Sarivalasis (A)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.

Leyder Elena Lozano (LE)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Tania Wyss (T)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland; Bioinformatics Core Facility, Swiss Institute of Bioinformatics (SIB), Lausanne, Switzerland.

Susana Inoges (S)

Division of Immunology and Immunotherapy, Center for Applied Medical Researckh, University of Navarra, Pamplona, Spain; Instituto de Investigación Sanitaria de Navarra, Pamplona, Spain; University Clinic, University of Navarra, Pamplona, Spain; Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain.

Ingrid Jolanda Monique de Vries (IJM)

Department of Tumour Immunology, Radboud Institute of Molecular Life Sciences, Geert Grooteplein 26-28, 6525 GA, Nijmegen, the Netherlands; Department of Medical Oncology, Radboudumc, Geert Grooteplein Zuid 10, 6525, GA, Nijmegen, the Netherlands.

Florence Dartiguenave (F)

Urology Research Unit, Department of Urology, CHUV, Switzerland.

Patrice Jichlinski (P)

Urology Research Unit, Department of Urology, CHUV, Switzerland.

Laurent Derrè (L)

Urology Research Unit, Department of Urology, CHUV, Switzerland.

George Coukos (G)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Ignacio Melero (I)

Division of Immunology and Immunotherapy, Center for Applied Medical Researckh, University of Navarra, Pamplona, Spain; Instituto de Investigación Sanitaria de Navarra, Pamplona, Spain; University Clinic, University of Navarra, Pamplona, Spain; Centro de Investigación Biomédica en Red Cáncer, Madrid, Spain.

Alexandre Harari (A)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Pedro Romero (P)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland.

Selena Viganó (S)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland. Electronic address: selena.vigano@chuv.ch.

Lana Elias Kandalaft (LE)

Department of Oncology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland; Ludwig Institute for Cancer Research, University of Lausanne, Lausanne, Switzerland. Electronic address: lana.kandalaft@chuv.ch.

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