Smoking reduces circulating CD26hi CD161hi MAIT cells in healthy individuals and patients with multiple sclerosis

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Cecilie Ammitzbøll
  • Lars Börnsen
  • Jeppe Romme Christensen
  • Rikke Ratzer
  • Birgitte Romme Nielsen
  • Helle B Søndergaard
  • Marina R von Essen
  • Sellebjerg, Finn Thorup

Upon chronic cigarette smoke exposure, inhaled antigens and irritants cause altered lung immune homeostasis. Circulating immune cells are affected, and smoking is associated with an increased risk of developing various disorders, including multiple sclerosis (MS). This study was conducted to determine the impact of smoking on circulating immune cell subsets. Furthermore, we determined whether any smoking-associated changes were related to MS. With the use of flow cytometry, CFSE assays, and ELISpot assays, we analyzed circulating immune cell phenotypes and quantified antigen-induced proliferation and cytokine secretion in smokers and nonsmokers in a cohort of 100 healthy individuals (HI). In addition, we analyzed immune cell subsets associated with smoking in 2 independent cohorts of patients with MS. In HI smokers compared with nonsmokers, we found increased blood cell counts of granulocytes, monocytes, and lymphocytes. These cells were not more proinflammatory, autoreactive, or EBV reactive compared with cells from nonsmokers. Phenotypic differences were seen in plasmacytoid dendritic cells (pDCs) and CD8+T cells as higher percentages of ICOS ligand (ICOSL)+pDCs and lower percentages of CD26hiCD161hiCD8+T cells and CCR6+CD8+T cells in smokers compared with nonsmokers. In supplemental analyses, we showed that CD26hiCD161hiCD8+T cells were mainly mucosal-associated invariant T cells (MAITs). Comparable frequencies of ICOSL+pDCs, CCR6+CD8+T cells, and CD26hiCD161hiCD8+T cells were found between HI and MS patients who were nonsmokers. Our findings suggest general proinflammatory effects from smoking combined with skewing of specific cell populations in HI and MS patients. The function of these cell populations needs further investigation.

TidsskriftJournal of Leukocyte Biology
Udgave nummer5
Sider (fra-til)1211-1220
StatusUdgivet - maj 2017

ID: 194909964