Analysis of tumor-infiltrating CD103 resident memory T-cell content in recurrent laryngeal squamous cell carcinoma.
Antigens, CD
/ immunology
CD4-Positive T-Lymphocytes
/ immunology
CD8-Positive T-Lymphocytes
/ immunology
Carcinoma, Squamous Cell
/ immunology
Disease-Free Survival
Female
Head and Neck Neoplasms
/ immunology
Humans
Immunologic Memory
/ immunology
Integrin alpha Chains
/ immunology
Lymphocytes, Tumor-Infiltrating
/ immunology
Male
Middle Aged
Multivariate Analysis
Neoplasm Recurrence, Local
Prognosis
CD103
HNSCC
Larynx
Resident memory
T-cell
Journal
Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
received:
19
05
2018
accepted:
04
10
2018
pubmed:
27
10
2018
medline:
26
2
2019
entrez:
27
10
2018
Statut:
ppublish
Résumé
Recurrent laryngeal squamous cell carcinomas (LSCCs) are associated with poor outcomes, without reliable biomarkers to identify patients who may benefit from adjuvant therapies. Given the emergence of tumor-infiltrating lymphocytes (TIL) as a biomarker in head and neck squamous cell carcinoma, we generated predictive models to understand the utility of CD4 Tissue microarrays were constructed from salvage laryngectomy specimens of 183 patients with recurrent/persistent LSCC and independently stained for CD4 High tumor CD103 An immune profile driven by CD103
Sections du résumé
BACKGROUND
BACKGROUND
Recurrent laryngeal squamous cell carcinomas (LSCCs) are associated with poor outcomes, without reliable biomarkers to identify patients who may benefit from adjuvant therapies. Given the emergence of tumor-infiltrating lymphocytes (TIL) as a biomarker in head and neck squamous cell carcinoma, we generated predictive models to understand the utility of CD4
METHODS
METHODS
Tissue microarrays were constructed from salvage laryngectomy specimens of 183 patients with recurrent/persistent LSCC and independently stained for CD4
RESULTS
RESULTS
High tumor CD103
CONCLUSIONS
CONCLUSIONS
An immune profile driven by CD103
Identifiants
pubmed: 30361882
doi: 10.1007/s00262-018-2256-3
pii: 10.1007/s00262-018-2256-3
pmc: PMC6375747
mid: NIHMS996721
doi:
Substances chimiques
Antigens, CD
0
Integrin alpha Chains
0
alpha E integrins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
213-220Subventions
Organisme : NIH HHS
ID : F31-DE-027600-01
Pays : United States
Organisme : NIDCR NIH HHS
ID : U01 DE025184
Pays : United States
Organisme : NIDCR NIH HHS
ID : F31 DE027600
Pays : United States
Organisme : NIH HHS
ID : R01-CA194536
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA140044
Pays : United States
Organisme : NIDCD NIH HHS
ID : T32 DC005356
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA046592
Pays : United States
Organisme : NIH HHS
ID : U01-DE025184
Pays : United States
Organisme : NIH HHS
ID : P30-CA046592
Pays : United States
Organisme : NIH HHS
ID : T32-DC535615
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA194536
Pays : United States
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