Targeted spatial proteomic analysis of CD8

cytotoxic T lymphocytes (CTL) head and neck (H&N) cancer immune check point myeloid cell spatial proteomics tonsillar cancer

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2023
Historique:
received: 05 07 2023
accepted: 03 11 2023
medline: 4 12 2023
pubmed: 4 12 2023
entrez: 4 12 2023
Statut: epublish

Résumé

Tonsillar cancer is caused by high-risk human papillomavirus (HPV), tobacco smoking, and alcohol abuse. Aspects of the patient's immune response to this disease have arisen as prognostic factors and treatment targets, reflecting differences in the type and protein expression profile of immune cells. Because tonsillar cancers are heterogenous lesions such data need to be spatially resolved. In this study, we aim to explore inter-patient and intra-tumoral sources of variation in tonsillar cancer using immunofluorescence and targeted spatial proteomics to interrogate a cohort of 105 patients. Furthermore, we assess prognostic factors and elucidate molecular targets. We have used CD8, CD11c, and Pan-cytokeratin (PanCK) to quantify and locate immune cells driving antigen-specific cellular immunity. Guided by immunofluorescence information, we selected 355 CD8 Quantitative analysis of immunofluorescence in combination with clinical data revealed that the abundance of total CD8 Our findings highlight the relevance of analyzing aspects of tumor micro-architecture in the search of prognostic markers and molecular targets for tonsillar cancer. The abundance of intra-tumoral CD8

Sections du résumé

Background UNASSIGNED
Tonsillar cancer is caused by high-risk human papillomavirus (HPV), tobacco smoking, and alcohol abuse. Aspects of the patient's immune response to this disease have arisen as prognostic factors and treatment targets, reflecting differences in the type and protein expression profile of immune cells. Because tonsillar cancers are heterogenous lesions such data need to be spatially resolved.
Methods UNASSIGNED
In this study, we aim to explore inter-patient and intra-tumoral sources of variation in tonsillar cancer using immunofluorescence and targeted spatial proteomics to interrogate a cohort of 105 patients. Furthermore, we assess prognostic factors and elucidate molecular targets. We have used CD8, CD11c, and Pan-cytokeratin (PanCK) to quantify and locate immune cells driving antigen-specific cellular immunity. Guided by immunofluorescence information, we selected 355 CD8
Results UNASSIGNED
Quantitative analysis of immunofluorescence in combination with clinical data revealed that the abundance of total CD8
Conclusion UNASSIGNED
Our findings highlight the relevance of analyzing aspects of tumor micro-architecture in the search of prognostic markers and molecular targets for tonsillar cancer. The abundance of intra-tumoral CD8

Identifiants

pubmed: 38044986
doi: 10.3389/fonc.2023.1253418
pmc: PMC10691541
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1253418

Informations de copyright

Copyright © 2023 Altunbulakli, Jimenez, Askmyr, Sobti, Swoboda, Greiff and Lindstedt.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Can Altunbulakli (C)

Department of Immunotechnology, Lund University, Lund, Sweden.

David G Jimenez (DG)

Department of Immunotechnology, Lund University, Lund, Sweden.

David Askmyr (D)

Department of Otorhinolaryngology (ORL), Head & Neck Surgery, Skåne University Hospital, Lund, Sweden.
Department of Clinical Sciences, Lund University, Lund, Sweden.

Aastha Sobti (A)

Department of Immunotechnology, Lund University, Lund, Sweden.

Sabine Swoboda (S)

Department of Otorhinolaryngology (ORL), Head & Neck Surgery, Skåne University Hospital, Lund, Sweden.
Department of Clinical Sciences, Lund University, Lund, Sweden.

Lennart Greiff (L)

Department of Otorhinolaryngology (ORL), Head & Neck Surgery, Skåne University Hospital, Lund, Sweden.
Department of Clinical Sciences, Lund University, Lund, Sweden.

Malin Lindstedt (M)

Department of Immunotechnology, Lund University, Lund, Sweden.
Department of Otorhinolaryngology (ORL), Head & Neck Surgery, Skåne University Hospital, Lund, Sweden.

Classifications MeSH