Effects of combustible cigarettes and heated tobacco products on immune cell-driven inflammation in chronic obstructive respiratory diseases

Author:

Kastratovic Nikolina12,Cekerevac Ivan134,Sekerus Vanesa56,Markovic Vladimir17,Arsenijevic Aleksandar17,Volarevic Ana18,Harrell Carl Randall9,Jakovljevic Vladimir10,Djonov Valentin11,Volarevic Vladislav12712ORCID

Affiliation:

1. Center for Research on Harmful Effects of Biological and Chemical Hazards, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

2. Department of Genetics, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

3. Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

4. Pulmonology Clinic, University Clinical Center Kragujevac , Kragujevac 34000, Serbia

5. Institute for Pulmonary Diseases of Vojvodina , Sremska Kamenica 21204, Serbia

6. Department of Biochemistry, Faculty of Medicine, University of Novi Sad , Novi Sad 21000, Serbia

7. Department of Microbiology and Immunology, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

8. Department of Psychology, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

9. Regenerative Processing Plant, LLC , Palm Harbor, FL, United States

10. Department of Physiology, Center of Excellence for Redox Balance Research in Cardiovascular and Metabolic Disorders, Faculty of Medical Sciences, University of Kragujevac , Kragujevac 34000, Serbia

11. Institute of Anatomy, University of Bern , Bern 3012, Switzerland

12. Faculty of Pharmacy Novi Sad , Novi Sad 21000, Serbia

Abstract

Abstract Since long-term effects of heated tobacco products (HTP) on the progression of chronic obstructive pulmonary disease (COPD) are unknown, we used COPD mice model to compare immune cell-dependent pathological changes in the lungs of animals which were exposed to HTP or combustible cigarettes (CCs). We also performed intracellular staining and flow cytometry analysis of immune cells which were present in the blood of CCs and HTP users who suffered from immune cell-driven chronic obstructive respiratory diseases. CCs enhanced NLRP3 inflammasome-dependent production of inflammatory cytokines in lung-infiltrated neutrophils and macrophages and increased influx of cytotoxic Th1, Th2, and Th17 lymphocytes in the lungs of COPD mice. Similarly, CCs promoted generation of inflammatory phenotype in circulating leukocytes of COPD patients. Opposite to CCs, HTP favored expansion of immunosuppressive, IL-10-producing, FoxP3-expressing T, NK, and NKT cells in inflamed lungs of COPD mice. Compared with CCs, HTP had weaker capacity to promote synthesis of inflammatory cytokines in lung-infiltrated immune cells. Significantly lower number of inflammatory neutrophils, monocytes, Th1, Th2, and Th17 lymphocytes were observed in the blood of patients who consumed HTP than in the blood of CCs users, indicating different effects of CCs and HTP on immune cells’ phenotype and function.

Funder

Foundation for a Smoke-Free World

Ministry of Science Republic of Serbia

Faculty of Medical Sciences University of Kragujevac

Publisher

Oxford University Press (OUP)

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