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Do alternative tobacco products induce less adverse respiratory risk than cigarettes?

RATIONALE: Due to the relatively short existence of alternative tobacco products, gaps exist in our current understanding of their long-term respiratory health effects. We therefore undertook the first-ever side-by-side comparison of the impact of chronic inhalation of aerosols emitted from electron...

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Autores principales: Bhat, Tariq A., Kalathil, Suresh G., Leigh, Noel, Hutson, Alan, Goniewicz, Maciej L., Thanavala, Yasmin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617138/
https://www.ncbi.nlm.nih.gov/pubmed/37907902
http://dx.doi.org/10.1186/s12931-023-02568-2
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author Bhat, Tariq A.
Kalathil, Suresh G.
Leigh, Noel
Hutson, Alan
Goniewicz, Maciej L.
Thanavala, Yasmin M.
author_facet Bhat, Tariq A.
Kalathil, Suresh G.
Leigh, Noel
Hutson, Alan
Goniewicz, Maciej L.
Thanavala, Yasmin M.
author_sort Bhat, Tariq A.
collection PubMed
description RATIONALE: Due to the relatively short existence of alternative tobacco products, gaps exist in our current understanding of their long-term respiratory health effects. We therefore undertook the first-ever side-by-side comparison of the impact of chronic inhalation of aerosols emitted from electronic cigarettes (EC) and heated tobacco products (HTP), and combustible cigarettes (CC) smoke. OBJECTIVES: To evaluate the potential differential effects of alternative tobacco products on lung inflammatory responses and efficacy of vaccination in comparison to CC. METHODS: Mice were exposed to emissions from EC, HTP, CC, or air for 8 weeks. BAL and lung tissue were analyzed for markers of inflammation, lung damage, and oxidative stress. Another group was exposed for 12 weeks and vaccinated and challenged with a bacterial respiratory infection. Antibody titers in BAL and sera and pulmonary bacterial clearance were assessed. MAIN RESULTS: EC- and HTP-aerosols significantly augmented lung immune cell infiltrates equivalent to that achieved following CC-exposure. HTP and CC significantly increased neutrophil numbers compared to EC. All products augmented numbers of B cells, T cells, and pro-inflammatory IL17A(+) T cells in the lungs. Decreased lung antioxidant activity and lung epithelial and endothelial damage was induced by all products. EC and HTP differentially augmented inflammatory cytokines/chemokines in the BAL. Generation of immunity following vaccination was impaired by EC and HTP but to a lesser extent than CC, with a CC > HTP > EC hierarchy of suppression of pulmonary bacterial clearance. CONCLUSIONS: HTP and EC-aerosols induced a proinflammatory pulmonary microenvironment, lung damage, and suppressed efficacy of vaccination. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-023-02568-2.
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spelling pubmed-106171382023-11-01 Do alternative tobacco products induce less adverse respiratory risk than cigarettes? Bhat, Tariq A. Kalathil, Suresh G. Leigh, Noel Hutson, Alan Goniewicz, Maciej L. Thanavala, Yasmin M. Respir Res Research RATIONALE: Due to the relatively short existence of alternative tobacco products, gaps exist in our current understanding of their long-term respiratory health effects. We therefore undertook the first-ever side-by-side comparison of the impact of chronic inhalation of aerosols emitted from electronic cigarettes (EC) and heated tobacco products (HTP), and combustible cigarettes (CC) smoke. OBJECTIVES: To evaluate the potential differential effects of alternative tobacco products on lung inflammatory responses and efficacy of vaccination in comparison to CC. METHODS: Mice were exposed to emissions from EC, HTP, CC, or air for 8 weeks. BAL and lung tissue were analyzed for markers of inflammation, lung damage, and oxidative stress. Another group was exposed for 12 weeks and vaccinated and challenged with a bacterial respiratory infection. Antibody titers in BAL and sera and pulmonary bacterial clearance were assessed. MAIN RESULTS: EC- and HTP-aerosols significantly augmented lung immune cell infiltrates equivalent to that achieved following CC-exposure. HTP and CC significantly increased neutrophil numbers compared to EC. All products augmented numbers of B cells, T cells, and pro-inflammatory IL17A(+) T cells in the lungs. Decreased lung antioxidant activity and lung epithelial and endothelial damage was induced by all products. EC and HTP differentially augmented inflammatory cytokines/chemokines in the BAL. Generation of immunity following vaccination was impaired by EC and HTP but to a lesser extent than CC, with a CC > HTP > EC hierarchy of suppression of pulmonary bacterial clearance. CONCLUSIONS: HTP and EC-aerosols induced a proinflammatory pulmonary microenvironment, lung damage, and suppressed efficacy of vaccination. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-023-02568-2. BioMed Central 2023-10-31 2023 /pmc/articles/PMC10617138/ /pubmed/37907902 http://dx.doi.org/10.1186/s12931-023-02568-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Bhat, Tariq A.
Kalathil, Suresh G.
Leigh, Noel
Hutson, Alan
Goniewicz, Maciej L.
Thanavala, Yasmin M.
Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title_full Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title_fullStr Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title_full_unstemmed Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title_short Do alternative tobacco products induce less adverse respiratory risk than cigarettes?
title_sort do alternative tobacco products induce less adverse respiratory risk than cigarettes?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10617138/
https://www.ncbi.nlm.nih.gov/pubmed/37907902
http://dx.doi.org/10.1186/s12931-023-02568-2
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