Collapse of the Plasmacytoid Dendritic Cell Compartment in Advanced Cutaneous Melanomas by Components of the Tumor Cell Secretome.
Adult
Aged
Aged, 80 and over
Chemokines
/ immunology
Dendritic Cells
/ immunology
Disease Progression
Female
Humans
Male
Melanoma
/ genetics
Middle Aged
Proto-Oncogene Proteins B-raf
/ genetics
Proto-Oncogene Proteins p21(ras)
/ genetics
Sentinel Lymph Node
/ immunology
Skin Neoplasms
/ genetics
Young Adult
Melanoma, Cutaneous Malignant
Journal
Cancer immunology research
ISSN: 2326-6074
Titre abrégé: Cancer Immunol Res
Pays: United States
ID NLM: 101614637
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
07
03
2018
revised:
16
08
2018
accepted:
01
11
2018
pubmed:
8
11
2018
medline:
5
3
2020
entrez:
8
11
2018
Statut:
ppublish
Résumé
Melanoma is an immunogenic neoplasm infiltrated by T cells, although these adaptive T cells usually fail to eradicate the tumor. Plasmacytoid dendritic cells (PDCs) are potent regulators of the adaptive immune response and can eliminate melanoma cells via TLR-mediated effector functions. The PDC compartment is maintained by progressively restricted bone marrow progenitors. Terminally differentiated PDCs exit the bone marrow into the circulation, then home to lymph nodes and inflamed peripheral tissues. Infiltration by PDCs is documented in various cancers. However, their role within the melanoma immune contexture is not completely known. We found that in locoregional primary cutaneous melanoma (PCM), PDC infiltration was heterogeneous, occurred early, and was recurrently localized at the invasive margin, the site where PDCs interact with CD8
Identifiants
pubmed: 30401679
pii: 2326-6066.CIR-18-0141
doi: 10.1158/2326-6066.CIR-18-0141
doi:
Substances chimiques
Chemokines
0
KRAS protein, human
0
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Proto-Oncogene Proteins p21(ras)
EC 3.6.5.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
12-28Commentaires et corrections
Type : ErratumIn
Informations de copyright
©2018 American Association for Cancer Research.