Immune Cell Deconvolution Reveals Possible Association of γδ T Cells with Poor Survival in Head and Neck Squamous Cell Carcinoma

Author:

Parikh Anuraag S.12,Li Yize34ORCID,Mazul Angela5,Yu Victoria X.1,Thorstad Wade6,Rich Jason5,Paniello Randal C.5,Caruana Salvatore M.1,Troob Scott H.1,Jackson Ryan S.5,Pipkorn Patrik5,Zolkind Paul5,Qi Zongtai5,Adkins Douglas3,Ding Li3478,Puram Sidharth V.578ORCID

Affiliation:

1. Department of Otolaryngology—Head and Neck Surgery, Columbia University Irving Medical Center, New York, NY 10032, USA

2. Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY 10032, USA

3. Department of Medicine, Division of Oncology, Washington University in St. Louis, St. Louis, MO 63110, USA

4. McDonnell Genome Institute, Washington University in St. Louis, St. Louis, MO 63108, USA

5. Department of Otolaryngology—Head and Neck Surgery, Washington University School of Medicine, St. Louis, MO 63108, USA

6. Department of Radiation Oncology, Washington University in St. Louis, St. Louis, MO 63110, USA

7. Siteman Cancer Center, Washington University in St. Louis, St. Louis, MO 63108, USA

8. Department of Genetics, Washington University School of Medicine, St. Louis, MO 63108, USA

Abstract

(1) Background: The role of rare immune cell subtypes in many solid tumors, chief among them head and neck squamous cell carcinoma (HNSCC), has not been well defined. The objective of this study was to assess the association between proportions of common and rare immune cell subtypes and survival outcomes in HNSCC. (2) Methods: In this cohort study, we utilized a deconvolution approach based on the CIBERSORT algorithm and the LM22 signature matrix to infer proportions of immune cell subtypes from 517 patients with untreated HPV-negative HNSCC from The Cancer Genome Atlas. We performed univariate and multivariable survival analysis, integrating immune cell proportions with clinical, pathologic, and genomic data. (3) Results: We reliably deconvolved 22 immune cell subtypes in most patients and found that the most common immune cell types were M0 macrophages, M2 macrophages, and memory resting CD4 T cells. In the multivariable analysis, we identified advanced N stage and the presence of γδ T cells as independently predictive of poorer survival. (4) Conclusions: We uncovered that γδ T cells in the tumor microenvironment were a negative predictor of survival among patients with untreated HNSCC. Our findings underscore the need to better understand the role of γδ T cells in HNSCC, including potential pro-tumorigenic mechanisms, and whether their presence may predict the need for alternative therapy approaches.

Funder

V Foundation

Cancer Research Foundation

Barnes Jewish Hospital Foundation

NCI

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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