Immune Trait Shifts in Association With Tobacco Smoking: A Study in Healthy Women

• Published in: Frontiers in immunology Vol. 12; p. 637974
• Main Authors: Piaggeschi, Giulia, Rolla, Simona, Rossi, Niccolò, Brusa, Davide, Naccarati, Alessio, Couvreur, Simon, Spector, Tim D., Roederer, Mario, Mangino, Massimo, Cordero, Francesca, Falchi, Mario, Visconti, Alessia
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 09.03.2021
• Subjects: Adult; Aged; B-Lymphocytes - immunology; CD4 Lymphocyte Count; CD4-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - immunology; epidemiology; Female; Humans; immune cell subset frequencies; immune traits; Immunologic Memory - immunology; Immunology; Inflammation - immunology; leukocyte-shift; Lymphocyte Activation - immunology; Lymphocyte Subsets - immunology; Middle Aged; Monocytes - immunology; Smoking - adverse effects; Smoking - immunology; Smoking Cessation; tobacco smoking exposure; epidemiology; immune cell subset frequencies; immune traits; leukocyte-shift; tobacco smoking exposure
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2021.637974

Tobacco smoking is known to impact circulating levels of major immune cells populations, but its effect on specific immune cell subsets remains poorly understood. Here, using high-resolution data from 223 healthy women (25 current and 198 never smokers), we investigated the association between smoking status and 35,651 immune traits capturing immune cell subset frequencies. Our results confirmed that active tobacco smoking is associated with increased frequencies of circulating CD8+ T cells expressing the CD25 activation marker. Moreover, we identified novel associations between smoking status and relative abundances of CD8+ CD25+ memory T cells, CD8+ memory T cells expressing the CCR4 chemokine receptor, and CD4+CD8+ (double-positive) CD25+ T cells. We also observed, in current smokers, a decrease in the relative frequencies of CD4+ T cells expressing the CD38 activation marker and an increase in class-switched memory B cell isotypes IgA, IgG, and IgE. Finally, using data from 135 former female smokers, we showed that the relative frequencies of immune traits associated with active smoking are usually completely restored after smoking cessation, with the exception of subsets of CD8+ and CD8+ memory T cells, which persist partially altered. Our results are consistent with previous findings and provide further evidence on how tobacco smoking shapes leukocyte cell subsets proportion toward chronic inflammation.