Marked up-regulation of T lymphocytes and expression of interleukin-9 in bronchial biopsies from patients With chronic bronchitis with obstruction

Chest. 2003 Nov;124(5):1909-15. doi: 10.1378/chest.124.5.1909.

Abstract

Study objective: To examine the differences in the inflammatory cell and cytokine profile between patients with chronic bronchitis (CB) with and without airway obstruction compared to control subjects.

Design: We used bronchial biopsy samples from the patients and control subjects and analyzed them for the presence of CD3 T cells, CD68, major basic protein (MBP), elastase, and tryptase, as well as expression of messenger RNA (mRNA) coding for interleukin (IL)-4, IL-5, interferon (IFN)-gamma, IL-9, eotaxin, and IFN-gamma-inducible protein (IP)-10. The techniques of immunocytochemistry and in situ hybridization were used. Results were expressed as the number of immunoreactive and mRNA-positive cells per field.

Results: Increased number of elastase, CD68, and MBP-positive cells (n = 9, p < 0.01) was demonstrated in both groups of patients with CB compared to control subjects. In patients with CB and obstruction, the number of elastase, CD68, and the number of CD3-positive cells was significantly increased compared to patients with CB without obstruction (n = 9, p < 0.01). IFN-gamma mRNA expression was increased in both groups of patients with CB compared to control subjects (n = 9, p < 0.01). IL-9 mRNA was significantly increased only in patients with CB and obstruction (n = 9, p < 0.01). Co-localization studies demonstrated > 80% of all IL-9-positive cells to be CD3-positive T cells. IP-10 mRNA was significantly increased in both groups of patients with CB compared to control subjects (n = 9, p < 0.01).

Conclusions: These results indicate a differential expression of inflammatory markers and cytokine mRNA in patients with obstructive CB. Increased presence of T lymphocytes and up-regulation of IL-9 and IP-10 mRNA expression in the bronchial biopsy samples may contribute to the airway obstruction in these patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Biopsy, Needle
  • Blood Proteins / metabolism
  • Bronchi / pathology*
  • Bronchitis, Chronic / complications
  • Bronchitis, Chronic / metabolism*
  • Bronchitis, Chronic / pathology
  • CD3 Complex / analysis
  • Chemokine CCL11
  • Chemokines, CC / metabolism
  • Cytokines / metabolism
  • Eosinophil Granule Proteins
  • Eosinophils / pathology
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Inflammation
  • Interleukin-9 / biosynthesis*
  • Macrophages / pathology
  • Male
  • Middle Aged
  • Neutrophils / pathology
  • Pancreatic Elastase / metabolism
  • Pulmonary Disease, Chronic Obstructive / complications
  • Pulmonary Disease, Chronic Obstructive / metabolism*
  • Pulmonary Disease, Chronic Obstructive / pathology
  • Ribonucleases / metabolism
  • T-Lymphocytes / metabolism*
  • Up-Regulation*

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Blood Proteins
  • CCL11 protein, human
  • CD3 Complex
  • CD68 antigen, human
  • Chemokine CCL11
  • Chemokines, CC
  • Cytokines
  • Eosinophil Granule Proteins
  • Interleukin-9
  • Ribonucleases
  • Pancreatic Elastase