Regulatory T-Cell Distribution within Lung Compartments in COPD

COPD. 2017 Oct;14(5):533-542. doi: 10.1080/15412555.2017.1346069. Epub 2017 Jul 26.

Abstract

The importance of the adaptive immune response, specifically the role of regulatory T (Treg) cells in controlling the obstruction progression in smokers, has been highlighted. To quantify the adaptive immune cells in different lung compartments, we used lung tissues from 21 never-smokers without lung disease, 22 current and/or ex-smokers without lung disease (NOS) and 13 current and/or ex-smokers with chronic obstructive pulmonary disease (COPD) for histological analysis. We observed increased T, B, IL-17 and BAFF+ cells in small and large airways of COPD individuals; however, in the NOS, we only observed increase in T and IL-17+ cells only in small airways. A decrease in the density of Treg+, TGF-β+ and IL-10+ in small and large airways was observed only in COPD individuals. In the lymphoid tissues, Treg, T,B-cells and BAFF+ cells were also increased in COPD; however, changes in Treg inhibitory associated cytokines were not observed in this compartment. Therefore, our results suggest that difference in Treg+ cell distributions in lung compartments and the decrease in TGF-β+ and IL-10+ cells in the airways may lead to the obstruction in smokers.

Keywords: Adaptive immunity; COPD; T-cells; TGF-β; interleukin-10; regulatory T-cells.

MeSH terms

  • Adaptive Immunity
  • Adult
  • Aged
  • B-Cell Activating Factor / metabolism
  • B-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Female
  • Forced Expiratory Volume
  • Humans
  • Interleukin-10 / metabolism
  • Interleukin-17 / metabolism
  • Lung / immunology*
  • Lymphocyte Count
  • Lymphoid Tissue / immunology*
  • Male
  • Middle Aged
  • Pulmonary Disease, Chronic Obstructive / immunology*
  • Pulmonary Disease, Chronic Obstructive / pathology
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Smoking / immunology*
  • Smoking / pathology
  • Smoking / physiopathology
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Transforming Growth Factor beta / metabolism
  • Vital Capacity

Substances

  • B-Cell Activating Factor
  • Interleukin-17
  • TNFSF13B protein, human
  • Transforming Growth Factor beta
  • Interleukin-10