RESEARCH BACKGROUND \& RATIONALE
Chronic rhinosinusitis (CRS) can manifest as T2 and/or non-T2 inflammation patterns, independently of the presence or absence of nasal polyps (NP). Certain aspects of CRS, such as NP formation, have been associated with epigenetic processes. Numerous studies support a role for epigenetics in the development and chronicity of other T2 diseases e.g. asthma and allergic rhinitis (North, Ann Allergy Asthma Immunol, 2011).
An insight into T2 disease pathogenesis may have been afforded by the "real-world" experiences during the COVID19 pandemic. Viral containment measures deployed in 2020 predictably reduced the frequency of most common respiratory viruses, reducing invasive respiratory infections along with exacerbations of asthma and COPD, which are typically triggered by viral respiratory infections (Linden, Eur Respir Rev, 2019; Mikhail, Ann Allergy Asthma Immunol, 2019). Unexpectedly, chronic inflammation of the upper airways was also reduced. Chronic otitis media with effusion and adenoiditis plummeted, and over half of the children on the waiting list for surgery the investigators removed because of spontaneous improvement. This was accompanied by anecdotal observations of a reduction in consultations for chronic rhinosinusitis with nasal polyposis (CRSwNP).
The investigators thus propose that T2 disease represents a unique facet of the inflammatory disease spectrum whereby dysfunction develops following interaction with a viral pathogen maintaining persistent effects via epigenetic mechanisms or chronic infection.
Detailed Research Plan Current understanding of T2 disease pathophysiology leaves early steps of pathogenesis largely unexplained. The investigators believe T2 disease is a result of epigenetic imprinting which reduces T1 response to injury or pathogens via impairment of Interferon (IFN) signaling components, leading to unopposed T2 signaling.
Furthermore, the investigators suspect that this dysfunction is produced by viral infection, which may persist in the host in latent form, or which may continue to exert its effects via epigenetic modifications of the host genome. In consequence, the investigators propose to comprehensively characterize the epigenetic modulations present in T2 inflammation, with a focus on demonstrating the link with viral infections. To reach our goal, the investigators will characterize T2 disease by combining DNA methylation status, chromatin accessibility and gene expression profiling to determine genes and epigenetic changes potentially important in the pathogenesis of T2 disease. The investigators will leverage the massive change in societal viral exposure imposed by pandemic measures as a unique experimental condition by comparing contemporary results with a biobank of pre- pandemic material. In addition to shedding new light on the pathogenesis, defining the epigenetic and virome portrait of T2 disease will improve new diagnostic and therapeutic targets, and potentially, identify implicated viruses.
Research strategy The investigators will identify epigenetic patterns and viruses associated with T2 CRSwNP patients . Taking advantage of an existing and extensive biobank of cells from tissue and biopsy samples, the investigators will compare epigenetics and viruses present pre-lockdown and per- pandemic in CRS and healthy patients. The population (detailed in the next section) includes healthy subjects, CRS patients under treatment in remission, and diseased patients undergoing endoscopic sinus surgery (ESS). The investigators aim to assess an equal number of both biological sexes to analyse potential differences. Sample size is based on previous transcriptomics experience. This observational study will not require any additional treatment to patients.
Experimental design
I) TYPE 2 AND METHYLATION:
Primary epithelial cells from CRSwNP biopsy samples (N=24) and control primary nasal epithelial cells from patients undergoing endoscopic pituitary surgery (N=16) Population: The investigators will use frozen dissociated cells from our biobank in earliest possible format (P0 or P1) to preserve original viruses and epigenetic marks. Polyp samples from T2 CRSwNP will be selected according to clinical phenotype together with blood test and histology.
II) PATIENTS IN REMISSION Methods: Experiments A, B and C will all use the following method for analysing brushing samples from the nasal cavity. (N=36) A) Establishing the virome and methylation profile in healthy upper airway cells. (N=12) B) What do healthy sinuses look like under medical treatment (N=12) C) Does reducing T2 inflammation with dupilumab work by increasing IFN activity or by reducing methylation in IFN pathway?
III) HOW DOES SURGERY EXERT AN EFFECT ON TYPE 2? Primary cross-sectional analysis and then compared to evolution at 4 months post-surgery Population: Patients undergoing ESS for CRSwNP, including at least 30% of subjects with aspirin sensitivity.
Phase I: At time of ESS (n= 24, plus 6 for validation of brushing) Methods: Patients will undergo a biopsy of the anterior ethmoid sinus. These will be undergo assessment using transcriptomic tools, including Single cell multiomes .
Phase II: 4 months post-ESS (n=the same 24 paired subjects. The same cohort of patients will be assessed at the four-month timepoint. Evolution of disease will be assessed according to CSO HNS standards into "Optimal" "Sub-optimal" or "Unacceptable" results. A brushing will be used for sampling and subjected to the same analyses as above.
