# Connecting the Airways: Current Trends in United Airway Diseases

**Authors:** Benedetta Bondi, Martina Buscema, Federico Di Marco, Carlo Conti, Andrea Caviglia, Lorenzo Fucci, Anna Maria Riccio, Marcello Mincarini, Martina Ottoni, Fulvio Braido, Rikki Frank Canevari, Diego Bagnasco

PMC · DOI: 10.3390/jpm16010021 · 2026-01-04

## TL;DR

This paper discusses how upper and lower airway diseases are interconnected and should be treated as a unified system.

## Contribution

It emphasizes the importance of a multidisciplinary approach for diagnosing and managing united airway diseases.

## Key findings

- Type 2 inflammation is central to many united airway disease phenotypes.
- Epithelial barrier dysfunction initiates shared inflammatory processes.
- Biologic therapies are effective for severe T2-high disease.

## Abstract

The concept of united airway disease (UAD) highlights the bidirectional relationship between inflammatory disorders of the upper airways—such as allergic rhinitis and chronic rhinosinusitis with or without nasal polyps (CRSwNP/CRSsNP)—and lower airway diseases, most notably asthma. This paradigm is supported by epidemiological, embryological, and immunological evidence demonstrating that airway inflammation represents a single, interconnected process rather than isolated compartmental pathology. Central to many UAD phenotypes is type 2 (T2) inflammation, driven by cytokines including IL-4, IL-5, and IL-13, and mediated by effector cells such as eosinophils and group 2 innate lymphoid cells (ILC2s). Epithelial barrier dysfunction often serves as the initiating trigger for this shared inflammatory cascade by production of TSLP, IL-25 and IL-33. Optimal diagnosis and management of UAD require an integrated, multidisciplinary framework. Clinical evaluation remains essential for patient characterization but must be complemented by pheno-endotypic assessment using imaging (CT), allergy testing, biomarker profiling (FeNO, blood eosinophils, IgE), and pulmonary function testing (spirometry, impulse oscillometry). Therapeutic strategies are layered, targeting both symptom control and inflammation across airway compartments. Standard approaches include intranasal and inhaled corticosteroids as well as saline irrigations, while severe T2-high disease increasingly benefits from biologic therapies (anti-IL-5/IL-5R, anti-IL-4R, anti-TSLP), which reduce dependence on systemic corticosteroids and surgical interventions such as endoscopic sinus surgery (ESS). Emerging precision-medicine models, particularly the “treatable traits” approach, further underscore the need to view the airway as a unified system. Collectively, these insights reinforce the clinical imperative of addressing upper and lower airway disease as a continuum, ensuring that inflammation in one district is neither overlooked nor treated in isolation.

## Linked entities

- **Proteins:** IL4 (interleukin 4), IL5 (interleukin 5), IL13 (interleukin 13), TSLP (thymic stromal lymphopoietin), IL25 (interleukin 25), IL33 (interleukin 33)
- **Diseases:** allergic rhinitis (MONDO:0011786), asthma (MONDO:0004979)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL5RA (interleukin 5 receptor subunit alpha) [NCBI Gene 3568] {aka CD125, CDw125, HSIL5R3, IL5R}, IL25 (interleukin 25) [NCBI Gene 64806] {aka IL17E}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL4R (interleukin 4 receptor) [NCBI Gene 3566] {aka CD124, IL-4RA, IL4RA}
- **Diseases:** airway inflammation (MESH:D007249), allergy (MESH:D004342), Airway Diseases (MESH:D029424), chronic rhinosinusitis (MESH:D000092562), allergic rhinitis (MESH:D065631), asthma (MESH:D001249), nasal polyps (MESH:D009298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12843504/full.md

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Source: https://tomesphere.com/paper/PMC12843504