Respiratory Effects of Exposure to Aerosol From the Candidate Modified-Risk Tobacco Product THS 2.2 in an 18-Month Systems Toxicology Study With A/J Mice

Author:

Titz Bjoern1,Sewer Alain1,Luettich Karsta1ORCID,Wong Ee Tsin2,Guedj Emmanuel1,Nury Catherine1,Schneider Thomas3,Xiang Yang1,Trivedi Keyur1,Vuillaume Grégory1,Leroy Patrice1,Büttner Ansgar4,Martin Florian1,Ivanov Nikolai V1,Vanscheeuwijck Patrick1,Hoeng Julia1,Peitsch Manuel C1

Affiliation:

1. PMI R&D, Philip Morris Products S.A, CH-2000 Neuchâtel, Switzerland

2. Philip Morris International Research Laboratories Pte. Ltd, Singapore 117406

3. Biognosys AG, 8952 Schlieren, Switzerland

4. Histovia GmbH, 51491 Overath, Germany

Abstract

Abstract Smoking cessation is the most effective measure for reducing the risk of smoking-related diseases. However, switching to less harmful products (modified-risk tobacco products [MRTP]) can be an alternative to help reduce the risk for adult smokers who would otherwise continue to smoke. In an 18-month chronic carcinogenicity/toxicity study in A/J mice (OECD Test Guideline 453), we assessed the aerosol of Tobacco Heating System 2.2 (THS 2.2), a candidate MRTP based on the heat-not-burn principle, compared with 3R4F cigarette smoke (CS). To capture toxicity- and disease-relevant mechanisms, we complemented standard toxicology endpoints with in-depth systems toxicology analyses. In this part of our publication series, we report on integrative assessment of the apical and molecular exposure effects on the respiratory tract (nose, larynx, and lungs). Across the respiratory tract, we found changes in inflammatory response following 3R4F CS exposure (eg, antimicrobial peptide response in the nose), with both shared and distinct oxidative and xenobiotic responses. Compared with 3R4F CS, THS 2.2 aerosol exerted far fewer effects on respiratory tract histology, including adaptive tissue changes in nasal and laryngeal epithelium and inflammation and emphysematous changes in the lungs. Integrative analysis of molecular changes confirmed the substantially lower impact of THS 2.2 aerosol than 3R4F CS on toxicologically and disease-relevant molecular processes such as inflammation, oxidative stress responses, and xenobiotic metabolism. In summary, this work exemplifies how apical and molecular endpoints can be combined effectively for toxicology assessment and further supports findings on the reduced respiratory health risks of THS 2.2 aerosol.

Funder

Philip Morris International

Publisher

Oxford University Press (OUP)

Subject

Toxicology

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