Multi-scaled transcriptomics of chronically inflamed nasal epithelium reveals immune-epithelial dynamics and tissue remodeling in nasal polyp formation

Chronic rhinosinusitis (CRS) is a common chronic inflammatory disease of the sinonasal cavity affecting millions worldwide. Its complex pathophysiology remains poorly understood, with emerging evidence implicating interactions between diverse immune and epithelial cells in disease progression. We applied single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics to both dissociated and intact human tissues from individuals with CRS with and without nasal polyps and compared them with controls. We revealed mechanisms of macrophage-eosinophil recruitment, CD4<sup>+</sup> and CD8<sup>+</sup> T cell dysregulation, and mast cell enrichment. We identified key immune-epithelial interactions in tissue remodeling, particularly involving basal progenitor and tuft cells. A distinct basal cell trajectory was implicated in nasal polyp formation. Orthogonal validation with spatial transcriptomics from >100 individuals with CRS revealed conserved tissue remodeling features. Our study provides insights into CRS pathophysiology, highlighting immune-epithelial interactions as potential therapeutic targets in chronic inflammation, also serving as a resource for dissecting immune disease mechanisms.

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Publication Details

Journal
Immunity
Published
2025-09-13
DOI
https://doi.org/10.1016/j.immuni.2025.08.009
Citations
3
Primary Topic
Nasal Surgery and Airway Studies
Type
article
Field-Weighted Citation Impact
6.02
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article

Multi-scaled transcriptomics of chronically inflamed nasal epithelium reveals immune-epithelial dynamics and tissue remodeling in nasal polyp formation

Zihai Li, Matt Lechner, Angela Yang, Dawn T. Bravo et al.
3 citations
Immunity
Nasal Surgery and Airway Studies
6.02
article

Multi-scaled transcriptomics of chronically inflamed nasal epithelium reveals immune-epithelial dynamics and tissue remodeling in nasal polyp formation

Zihai Li, Matt Lechner, Angela Yang, Dawn T. Bravo, David Zarabanda, Nicole A. Borchard, Bokai Zhu, Vassiliki A. Boussiotis, Jonathan B. Overdevest, Qin Ma, Sizun Jiang, John A. Coller, Dingani Nkosi, Garry P. Nolan, Katie M. Phillips, Te‐Huei Yeh, Ivan T. Lee, Maria Serena Longhi, Tsuguhisa Nakayama, Cankun Wang, Dan H. Barouch, Axel Eluid Renteria, Dhananjay Wagh, Jayakar V. Nayak, Carol H. Yan, Chun‐Kang Liao, Sachi S. Dholakia, Jason Yeung, Peter H. Hwang, Yuzhou Chang, Yao Yu Yeo, Guanrui Liao, Philip A. Gall, Michael T. Chang, Zara M. Patel, Dayoung Kim
article en
3 citations

Abstract

Chronic rhinosinusitis (CRS) is a common chronic inflammatory disease of the sinonasal cavity affecting millions worldwide. Its complex pathophysiology remains poorly understood, with emerging evidence implicating interactions between diverse immune and epithelial cells in disease progression. We applied single-cell RNA sequencing (scRNA-seq) and spatial transcriptomics to both dissociated and intact human tissues from individuals with CRS with and without nasal polyps and compared them with controls. We revealed mechanisms of macrophage-eosinophil recruitment, CD4<sup>+</sup> and CD8<sup>+</sup> T cell dysregulation, and mast cell enrichment. We identified key immune-epithelial interactions in tissue remodeling, particularly involving basal progenitor and tuft cells. A distinct basal cell trajectory was implicated in nasal polyp formation. Orthogonal validation with spatial transcriptomics from >100 individuals with CRS revealed conserved tissue remodeling features. Our study provides insights into CRS pathophysiology, highlighting immune-epithelial interactions as potential therapeutic targets in chronic inflammation, also serving as a resource for dissecting immune disease mechanisms.

ImmunityVol. 58(10)
Brigham and Women's Hospital (US), Beth Israel Deaconess Medical Center (US), Harvard University (US), VA Palo Alto Health Care System (US), The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (US), University of California San Diego (US), Dana-Farber Cancer Institute (US), National Taiwan University Hospital (TW), University College London (GB), The Ohio State University (US), University of Cincinnati (US), National Yunlin University of Science and Technology (TW), Columbia University (US), Stanford University (US)
Openalex Percentile: Top 3%
Nasal Surgery and Airway Studies
6.02
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