Association of Suppressive Myeloid Cell Enrichment with Aggressive Oropharynx Squamous Cell Carcinoma

Author:

Yang Changlin1ORCID,Garg Rekha2,Fredenburg Kristanna3,Weidert Frances1,Mendez-Gomez Hector1,Amdur Robert4,Lee Ji-Hyun5,Ku Jamie6,Kresak Jesse3,Staras Stephanie7ORCID,Sikora Andrew G.8,Wang Lily9,McGrail Daniel10,Mitchell Duane1,Sayour Elias1,Silver Natalie610

Affiliation:

1. Department of Neurosurgery, University of Florida, Gainesville, FL 32608, USA

2. Department of Pediatrics, University of Florida, Gainesville, FL 32603, USA

3. Department of Pathology, University of Florida, Gainesville, FL 32610, USA

4. Department of Radiation Oncology, University of Florida, Gainesville, FL 32608, USA

5. Department of Biostatistics, University of Florida, Gainesville, FL 32603, USA

6. Head and Neck Institute, Cleveland Clinic, Cleveland, OH 44106, USA

7. Department of Health Outcomes and Biomedical Informatics, University of Florida, Gainesville, FL 32610, USA

8. Department of Head and Neck Surgery, MD Anderson Cancer Center, University of Texas, Houston, TX 77030, USA

9. Translational Hematology and Oncology, Cleveland Clinic, Cleveland, OH 44195, USA

10. Lerner Research Institute, Cleveland Clinic, Center of Immunotherapy and Precision Immuno-Oncology, Cleveland, OH 44106, USA

Abstract

Background: While immune-cell infiltrated tumors, such as human papillomavirus positive (HPV+) ororpharyngeal squamous cell carcinomas (OPSCC) have been associated with an improved clinical prognosis, there is evidence to suggest that OPSCCs are also subjected to increased immunoregulatory influence. The objective of this study was to assess whether patients with clinically aggressive OPSCC have a distinct immunosuppressive immune signature in the primary tumor. Methods: This retrospective case-control study analyzed 37 pre-treatment tissue samples from HPV+ and HPV-negative OPSCC patients treated at a single institution. The cases were patients with known disease recurrence and the controls were patients without disease recurrence. An mRNA-expression immune-pathway profiling was performed, and correlated to clinical outcomes. The TCGA head and neck cancer database was utilized to make comparisons with the institutional cohort. Results: In our cohort, HPV-negative and HPV+ patients with known disease recurrence both had significantly increased suppressive monoctyte/macrophage and granulocyte cell-expression-profile enrichment. Similar findings were found in the TCGA cohort when comparing HPV-negative to positive patients. Conclusions: our study demonstrates that patients with recurrent HPV+ OPSCC had suppressive monocyte/macrophage and granulocyte immune-cell enrichment, similar to those seen in the more aggressive HPV-negative OPSCC.

Funder

NIH/NIDCR

NCI/NIDCR sponsored

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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