Affiliation:
1. Department of Pathology Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
2. Graduate Program in Immunology Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
3. Stanford Medicine Stanford University School of Medicine Stanford California U.S.A.
4. Department of Otolaryngology‐Head and Neck Surgery Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
5. Department of Oncology Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
6. Department of Obstetrics and Gynecology Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
7. Molecular Microbiology and Immunology Johns Hopkins University School of Medicine Baltimore Maryland U.S.A.
Abstract
ObjectivesRecurrent respiratory papillomatosis (RRP) is caused by human papilloma virus (HPV) infection of the aerodigestive tract that significantly impacts quality‐of‐life including the ability to communicate and breathe. Treatment was traditionally limited to serial ablative procedures in the O.R. with possible local adjuvant therapy, but new systemic therapies, such as Vascular endothelial growth factor (VEGF) inhibitors, are showing significant promise. This study aims to determine whether rationale exists for combination therapeutic approaches using VEGF inhibitors and/or immune checkpoint blockade.MethodsUsing fresh specimens from the O.R., we performed flow cytometry on papilloma, normal adjacent tissue, and blood. Papilloma and surrounding tissue were examined for expression of PD‐L1, PD‐L2, Galectin‐9, VEGFR2, and VEGFR3. CD8+ and CD4+ T cells were assayed for expression of PD‐1, TIGIT, LAG3, and TIM3.ResultsOur data shows that papilloma tissue exhibits significantly higher levels of PD‐L1 and PD‐L2 compared to adjacent tissue. Elevated levels of the VEGF receptor VEGFR3 were also observed in papilloma tissue. When examining T cells within the papilloma, elevated PD‐1 and TIGIT expression was observed on CD8+ T cells, while levels of PD‐1, TIGIT, and TIM3 were elevated on CD4+ T cells compared to PBMCs. Heterogenous marker expression was observed between individuals.ConclusionsOur analysis shows that RRP tissue shows elevated levels of multiple immune check point targets and VEGFR3, with varied patterns unique to each papilloma patient. Some of these immune checkpoint markers already have novel immunotherapies available or in development, providing molecular rationale to offer these systemic treatments to selected patients affected by RRP alongside VEGF inhibitors. Laryngoscope, 2024
Funder
National Institutes of Health