Prognostic significance of myeloid immune cells and their spatial distribution in the colorectal cancer microenvironment.
Aged
Colorectal Neoplasms
/ immunology
Female
Fluorescent Antibody Technique
Granulocytes
/ immunology
HLA-DR Antigens
/ analysis
Humans
Lewis X Antigen
/ analysis
Lipopolysaccharide Receptors
/ analysis
Male
Microscopy, Fluorescence
Middle Aged
Monocytes
/ immunology
Phenotype
Predictive Value of Tests
Prognosis
Prospective Studies
Sialic Acid Binding Ig-like Lectin 3
/ analysis
Tumor Microenvironment
/ immunology
United States
anti-tumor immunity
colorectal cancer
innate immunity
myeloid cells
spatial analysis
tumor microenvironment
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:
04 2021
04 2021
Historique:
accepted:
18
03
2021
entrez:
1
5
2021
pubmed:
2
5
2021
medline:
18
12
2021
Statut:
ppublish
Résumé
Myeloid cells represent an abundant yet heterogeneous cell population in the colorectal cancer microenvironment, and their roles remain poorly understood. We used multiplexed immunofluorescence combined with digital image analysis to identify CD14 Higher intraepithelial ( Myeloid cell populations occur in spatially distinct distributions and exhibit divergent, subset-specific prognostic significance in colorectal cancer, with mature CD14
Sections du résumé
BACKGROUND
Myeloid cells represent an abundant yet heterogeneous cell population in the colorectal cancer microenvironment, and their roles remain poorly understood.
METHODS
We used multiplexed immunofluorescence combined with digital image analysis to identify CD14
RESULTS
Higher intraepithelial (
CONCLUSIONS
Myeloid cell populations occur in spatially distinct distributions and exhibit divergent, subset-specific prognostic significance in colorectal cancer, with mature CD14
Identifiants
pubmed: 33931472
pii: jitc-2020-002297
doi: 10.1136/jitc-2020-002297
pmc: PMC8098931
pii:
doi:
Substances chimiques
CD14 protein, human
0
CD33 protein, human
0
HLA-DR Antigens
0
Lewis X Antigen
0
Lipopolysaccharide Receptors
0
Sialic Acid Binding Ig-like Lectin 3
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NCI NIH HHS
ID : R35 CA197735
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA118553
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA248857
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA167552
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA137178
Pays : United States
Organisme : NIDDK NIH HHS
ID : K24 DK098311
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA186107
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA169141
Pays : United States
Organisme : NCI NIH HHS
ID : R03 CA197879
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA127003
Pays : United States
Organisme : NCI NIH HHS
ID : K07 CA190673
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA222940
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA230873
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA087969
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA055075
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA151993
Pays : United States
Organisme : NCI NIH HHS
ID : K07 CA188126
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA167552
Pays : United States
Informations de copyright
© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: SAV reports grants from Finnish Cultural Foundation and Orion Research Foundation sr during the conduct of the study. KF reports other from Uehera Memorial Foundation (overseas scholarship) during the conduct of the study. ATC reports grants and personal fees from Bayer Pharma AG and personal fees from Pfizer Inc. and Boehringer Ingelheim outside the submitted work. RN is currently an employee and shareholder of Pfizer Inc. She contributed to this study before she was employed by Pfizer Inc. CSF reports consulting role for Agios, Amylin Pharmaceuticals, Astra-Zeneca, Bain Capital, CytomX Therapeutics, Daiichi-Sankyo, Eli Lilly, Entrinsic Health, Evolveimmune Therapeutics, Genentech, Merck, Taiho, and Unum Therapeutics; he also serves as a Director for CytomX Therapeutics and owns unexercised stock options for CytomX and Entrinsic Health; he is a cofounder of Evolveimmune Therapeutics and has equity in this private company; he has provided expert testimony for Amylin Pharmaceuticals and Eli Lilly. JAM reports personal fees from COTA Healthcare and Taiho Pharmaceutical (for NCCN Grant Review Panel) outside the submitted work. MG reports grants from Bristol-Myers Squibb, Merck, and Servier outside the submitted work. JAN reports grants from NanoString and Illumina outside the submitted work. The other authors declare that they have no conflicts of interest.
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