Related Experiment Video
Updated: Oct 23, 2025

09:02
Infection of Primary Nasal Epithelial Cells Grown at an Air-Liquid Interface to Characterize Human Coronavirus-Host Interactions
Published on: September 22, 2023
1.7K
Respiratory epithelial cell responses to SARS-CoV-2 in COVID-19
James P Bridges1,2, Eszter K Vladar3, Hua Huang4
1Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, National Jewish Health, Denver, Colorado, USA bridgesj@njhealth.org.
Thorax
|August 18, 2021
Summary
This review contrasts COVID-19 progression in the upper airways and gas exchange regions of the lung. Distinct cellular targets and immune responses necessitate tailored therapies for each site.
Area of Science:
- Pulmonary Medicine
- Virology
- Immunology
Background:
- COVID-19 presents varied clinical stages impacting therapeutic strategies.
- Understanding disease progression in the pulmonary epithelium is crucial.
- Distinct cellular compositions and immune responses exist in conducting airways versus gas exchange regions.
Purpose of the Study:
- To provide background on COVID-19 progression within the pulmonary epithelium.
- To discuss therapeutic options based on infection location.
- To contrast infection dynamics in conducting airways and gas exchange lung portions.
Main Methods:
- Review of scientific literature on SARS-CoV-2 infection.
- Comparative analysis of cellular targets and immune responses.
- Discussion of therapeutic implications for different lung regions.
Main Results:
- SARS-CoV-2 targets ciliated cells in nasal airways, impairing mucociliary clearance with suppressed innate immunity.
- Alveolar type II cells are primary targets in gas exchange regions, leading to damage and potential acute respiratory distress syndrome.
- Asymptomatic individuals can transmit the virus despite productive infection.
Conclusions:
- Distinct therapeutic approaches are suggested for upper airway versus alveolar SARS-CoV-2 infections.
- Alveolar damage and hyperinflammation are key targets for severe COVID-19 therapies.
- Alveolar type II cell progenitor function may influence long-term lung sequelae.

