학술논문

Determinants of SARS-CoV-2 entry and replication in airway mucosal tissue and susceptibility in smokers
Document Type
article
Source
Cell Reports Medicine. 2(10)
Subject
Dental/Oral and Craniofacial Disease
Tobacco
Prevention
Biodefense
Pneumonia & Influenza
Emerging Infectious Diseases
Infectious Diseases
Pneumonia
Tobacco Smoke and Health
Clinical Research
Vaccine Related
Lung
2.1 Biological and endogenous factors
Aetiology
2.2 Factors relating to the physical environment
Infection
Respiratory
Good Health and Well Being
Aged
Aged
80 and over
Angiotensin-Converting Enzyme 2
COVID-19
Female
Gene Expression Regulation
Humans
Male
Middle Aged
Nasal Cavity
Respiratory Mucosa
SARS-CoV-2
Serine Endopeptidases
Smokers
Trachea
Viral Tropism
ACE2
IFN-β1
TMPRSS2
ciliated epithelial cell
nasal cavity
smoking
trachea
upper airway
Language
Abstract
Understanding viral tropism is an essential step toward reducing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transmission, decreasing mortality from coronavirus disease 2019 (COVID-19) and limiting opportunities for mutant strains to arise. Currently, little is known about the extent to which distinct tissue sites in the human head and neck region and proximal respiratory tract selectively permit SARS-CoV-2 infection and replication. In this translational study, we discover key variabilities in expression of angiotensin-converting enzyme 2 (ACE2) and transmembrane serine protease 2 (TMPRSS2), essential SARS-CoV-2 entry factors, among the mucosal tissues of the human proximal airways. We show that SARS-CoV-2 infection is present in all examined head and neck tissues, with a notable tropism for the nasal cavity and tracheal mucosa. Finally, we uncover an association between smoking and higher SARS-CoV-2 viral infection in the human proximal airway, which may explain the increased susceptibility of smokers to developing severe COVID-19. This is at least partially explained by differences in interferon (IFN)-β1 levels between smokers and non-smokers.