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Published on: October 22, 2020
Inflammatory phenotype modulation in the respiratory tract and systemic circulation of e-cigarette users: a pilot
Ibrahim M Sayed1, Jorge A Masso-Silva2,3, Ankita Mittal3
1Department of Pathology, University of California San Diego, La Jolla, California.
Chronic e-cigarette use alters immune responses, decreasing airway defenses and impairing monocyte function. Reducing e-cigarette use may help restore these critical host defenses against infection.
Area of Science:
- Immunology
- Respiratory Medicine
- Toxicology
Background:
- E-cigarette use is widespread, but its long-term health effects, particularly on inflammation and immunity, remain unclear.
- Understanding the impact of e-cigarette aerosol inhalation on host defenses is crucial for public health.
Purpose of the Study:
- To investigate changes in the inflammatory profile and monocyte function in chronic e-cigarette users.
- To evaluate the effects of reduced e-cigarette use on these inflammatory markers and immune cell responses.
Main Methods:
- A longitudinal pilot study involving e-cigarette users and healthy controls.
- Analysis of saliva, sputum, and blood samples for 38 proteins using multiplex assays.
- Assessment of circulating monocyte inflammatory responses to bacterial lipopolysaccharide.
Main Results:
- E-cigarette users showed decreased immunomodulatory proteins in airways and elevated cytokines/chemokines in circulation compared to controls.
- Specific alterations included lower IL-1 receptor antagonist (IL-1Ra) in saliva, higher IL-1Ra and GRO in sputum, and elevated TNFβ and VEGF in plasma.
- Monocytes from e-cigarette users exhibited blunted IL-8 and IL-6 release, indicating impaired response to bacterial challenge.
Conclusions:
- Chronic inhalation of e-cigarette aerosols significantly alters the inflammatory state in airways and systemic circulation.
- These alterations raise concerns for increased susceptibility to inflammatory and infectious diseases in long-term e-cigarette users.
- Reduced e-cigarette use may partially reverse some of these detrimental immune effects.
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