Prognostic impact of intra- and peritumoral immune cell subpopulations in head and neck squamous cell carcinomas – Comprehensive analysis of the TCGA-HNSC cohort and immunohistochemical validation on 101 patients Journal Article


Authors: Knebel, M.; Körner, S.; Kühn, J. P.; Wemmert, S.; Brust, L.; Smola, S.; Wagner, M.; Bohle, R. M.; Morris, L. G. T.; Pandey, A.; Schick, B.; Linxweiler, M.
Article Title: Prognostic impact of intra- and peritumoral immune cell subpopulations in head and neck squamous cell carcinomas – Comprehensive analysis of the TCGA-HNSC cohort and immunohistochemical validation on 101 patients
Abstract: Background: Due to the expanding role of immune checkpoint inhibition in the treatment of head and neck squamous cell carcinoma, understanding immunological processes in the tumor microevironment (TME) has strong translational importance. Though analytical methods for a comprehensive analysis of the immunological TME have constantly improved and expanded over the past years the prognostic relevance of immune cell composition in head and neck cancer TME largely remains ambiguous with most studies focusing on one or a small subset of immune cells. Methods: The overall survival (OS) of the TCGA-HNSC patient cohort comprising 513 head and neck cancer patients was correlated with a total of 29 different immune metrics including a wide spectrum of immune cell subpopulations as well as immune checkpoint receptors and cytokines using RNAseq based immune deconvolution analyses. The most significant predictors of survival among these 29 immune metrics were validated on a separate HNSCC patient cohort (n=101) using immunohistochemistry: CD3, CD20+CXCR5, CD4+CXCR5, Foxp3 and CD68. Results: Overall immune infiltration irrespective of immune cell composition showed no significant correlation with the patients’ overall survival in the TCGA-HNSC cohort. However, when focusing on different immune cell subpopulations, naïve B cells (p=0.0006), follicular T-helper cells (p<0.0001), macrophages (p=0.0042), regulatory T cells (p=0.0306), lymphocytes (p=0.0001), and cytotoxic T cells (p=0.0242) were identified as highly significant predictors of improved patient survival. Using immunohistochemical detection of these immune cells in a second independent validation cohort of 101 HNSCC patients, we confirmed the prognostic relevance of follicular T helper cells, cytotoxic T cells and lymphocytes. In multivariable analysis, HPV negativity and advanced UICC stages were identified as additional prognostic biomarkers associated with poor outcome. Conclusion: Our study highlights the prognostic relevance of the immunological tumor environment in head and neck cancer and demonstrates that a more detailed analysis of immune cell composition and immune cell subtypes is necessary to accurately prognosticate. We observed the highest prognostic relevance for lymphocytes, cytotoxic T cells, and follicular T helper cells, suggesting further investigations focusing on these specific immune cell subpopulations not only as predictors of patient prognosis but also as promising targets of new immunotherapeutic strategies. Copyright © 2023 Knebel, Körner, Kühn, Wemmert, Brust, Smola, Wagner, Bohle, Morris, Pandey, Schick and Linxweiler.
Keywords: immunohistochemistry; adult; controlled study; human tissue; middle aged; major clinical study; overall survival; cd3 antigen; transcription factor foxp3; biological marker; cell infiltration; smoking; b lymphocyte; b-lymphocytes; cd20 antigen; regulatory t lymphocyte; immunotherapy; head and neck neoplasms; cytotoxic t lymphocyte; t-lymphocytes, helper-inducer; cd4 antigen; macrophage; lymphocyte; immunocompetent cell; head and neck tumor; helper cell; cd68 antigen; head and neck squamous cell carcinoma; tumor microenvironment; cell composition; chemokine receptor cxcr5; the cancer genome atlas; deconvolution; humans; prognosis; human; male; female; article; rna sequencing; squamous cell carcinoma of head and neck; prognostic biomarkers; hnscc (head and neck squamous cell carcinoma); immunological tumor microenvironment
Journal Title: Frontiers in Immunology
Volume: 14
ISSN: 1664-3224
Publisher: Frontiers Media S.A.  
Date Published: 2023-01-01
Start Page: 1172768
Language: English
DOI: 10.3389/fimmu.2023.1172768
PUBMED: 37383237
PROVIDER: scopus
PMCID: PMC10294051
DOI/URL:
Notes: Article -- Source: Scopus
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  1. Luc Morris
    282 Morris