Increased Abundances of CD16

HPV PD-L1 T cells head and neck cancer monocyte subsets oropharyngeal cancer

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
09 Jun 2022
Historique:
received: 09 05 2022
revised: 07 06 2022
accepted: 08 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 25 6 2022
Statut: epublish

Résumé

Patients with human papilloma virus (HPV)-related oropharyngeal cancer have a better prognosis than nonvirally associated patients, most likely because of better immune responses. Increased infiltration of T lymphocytes into the oropharyngeal tumor tissue has been observed, but the dynamics of circulating lymphocytes and monocytes are not fully understood. The aim of this study was to understand the population dynamics of circulating monocyte subsets in oropharyngeal cancer (OPC) patients with regard to the clinicopathological parameters and accompanying immunological consequences in view of the CD4/CD8 T cell subset composition, and the expression of checkpoint pathway proteins programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1). The abundance of circulating monocyte subsets and peripheral blood CD4/CD8 T cells of oropharyngeal cancer patients and their PD-L1 and PD-1 expression levels were analyzed by flow cytometry. The studied oropharyngeal cancer patients revealed heterogeneous individual redistributions of CD14 We conclude that oropharyngeal cancer, as a malignancy from a lymphoid-tissue-rich anatomical region, has a strong systemic impact on the differentiation and regulation of circulating innate and adaptive immune cells. Further comprehensive investigations are required for the possible future usability of the described immunological alterations as bioliquid parameters for prognosis or therapy response prediction.

Sections du résumé

BACKGROUND BACKGROUND
Patients with human papilloma virus (HPV)-related oropharyngeal cancer have a better prognosis than nonvirally associated patients, most likely because of better immune responses. Increased infiltration of T lymphocytes into the oropharyngeal tumor tissue has been observed, but the dynamics of circulating lymphocytes and monocytes are not fully understood. The aim of this study was to understand the population dynamics of circulating monocyte subsets in oropharyngeal cancer (OPC) patients with regard to the clinicopathological parameters and accompanying immunological consequences in view of the CD4/CD8 T cell subset composition, and the expression of checkpoint pathway proteins programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1).
MATERIALS AND METHODS METHODS
The abundance of circulating monocyte subsets and peripheral blood CD4/CD8 T cells of oropharyngeal cancer patients and their PD-L1 and PD-1 expression levels were analyzed by flow cytometry.
RESULTS RESULTS
The studied oropharyngeal cancer patients revealed heterogeneous individual redistributions of CD14
CONCLUSION CONCLUSIONS
We conclude that oropharyngeal cancer, as a malignancy from a lymphoid-tissue-rich anatomical region, has a strong systemic impact on the differentiation and regulation of circulating innate and adaptive immune cells. Further comprehensive investigations are required for the possible future usability of the described immunological alterations as bioliquid parameters for prognosis or therapy response prediction.

Identifiants

pubmed: 35740384
pii: biomedicines10061363
doi: 10.3390/biomedicines10061363
pmc: PMC9219638
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Christian Idel (C)

Department of Otorhinolaryngology, University of Luebeck, 23538 Luebeck, Germany.

Christina Polasky (C)

Department of Otorhinolaryngology, University of Luebeck, 23538 Luebeck, Germany.

Julika Ribbat-Idel (J)

Department of Pathology, University of Luebeck, 23538 Luebeck, Germany.

Kristin Loyal (K)

Department of Otorhinolaryngology, University of Luebeck, 23538 Luebeck, Germany.

Sven Perner (S)

Department of Pathology, University of Luebeck, 23538 Luebeck, Germany.

Dirk Rades (D)

Department of Radiation Oncology, University of Luebeck, 23538 Luebeck, Germany.

Karl-Ludwig Bruchhage (KL)

Department of Otorhinolaryngology, University of Luebeck, 23538 Luebeck, Germany.

Ralph Pries (R)

Department of Otorhinolaryngology, University of Luebeck, 23538 Luebeck, Germany.

Classifications MeSH