Chronic rhinosinusitis with polyps (CRSwNP) is a significant health problem in the United States. This disorder, which is often particularly recalcitrant to medical and surgical therapy, is characterized by persistent eosinophilic inflammation of the sinonasal mucosa, with thickened secretions that are frequently colonized with micro-organisms. The cellular and molecular mechanisms that underlie CRSwNP remain poorly understood. The epithelium of nose and sinuses participates actively in host immunity, serving as a barrier and first line of defense against inhaled pathogens and other potential threats. In previous studies, we investigated how sinonasal epithelial cells (SNEC) contribute to CRSwNP through production of innate pro-eosinophilic mediators and by bidirectional communication with other immune cells. Our research using human tissue and mouse models have suggested that SNEC are triggered by epithelial damage to produce mediators that promote eosinophilic inflammation. We hypothesize that this pathway, involving innate lymphoid cells (ILCs), is a normal aspect of healing and repair. Our latest findings suggest that the populations of ILCs and epithelial basal progenitor cells differ in CRSwNP. To test the hypotheses regarding basal cell and ILC interaction, we will initially, in aim 1, examine sinus mucosa from patients with chronic sinus inflammatory disease to define subtypes of basal progenitor cells and explore their innate immune function and pro-eosinophilic mediator expression. We will also employ novel cell culture models to understand the properties of basal cell populations.
In aim 2, we will explore type 2 ILCs in CRSwNP and their interaction with basal cell populations, using cell culture models. Finally, in aim 3, we will investigate the innate immune activity of polyp basal cells in a modified cell culture model, and we will utilize genetically-modified mice and nasal inflammation models to explore the role of innate immune regulation of basal cells in healing and persistence of eosinophilic inflammation after injury. These studies will significantly advance current knowledge about CRSwNP and create an opportunity to develop innovative therapies for this debilitating and costly medical condition.

Public Health Relevance

Chronic rhinosinusitis with nasal polyps is a common and costly condition in the US that is often recalcitrant to current medical and surgical treatments. Our research has shown that the lining cells of the sinus mucous membrane produce factors that may be important in polyp inflammation, which we propose to further investigate in human sinus tissue and animal models. If successful, this work will improve our understanding of chronic rhinosinusitis with polyps and lead to a new opportunity to develop effective drugs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI132590-03
Application #
9864049
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Dong, Gang
Project Start
2018-03-07
Project End
2023-02-28
Budget Start
2020-03-01
Budget End
2021-02-28
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205