Marked up-regulation of T lymphocytes and expression of interleukin-9 in bronchial biopsies from patients With chronic bronchitis with obstruction
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
14605067
DOI
10.1378/chest.124.5.1909
PII: S0012-3692(15)33429-2
Knihovny.cz E-zdroje
- MeSH
- antigeny CD3 analýza MeSH
- antigeny diferenciační myelomonocytární metabolismus MeSH
- bronchy patologie MeSH
- CD antigeny metabolismus MeSH
- chemokin CCL11 MeSH
- chemokiny CC metabolismus MeSH
- chronická bronchitida komplikace metabolismus patologie MeSH
- chronická obstrukční plicní nemoc komplikace metabolismus patologie MeSH
- cytokiny metabolismus MeSH
- eozinofily patologie MeSH
- hybridizace in situ MeSH
- imunohistochemie MeSH
- interleukin-9 biosyntéza MeSH
- jehlová biopsie MeSH
- krevní proteiny metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- makrofágy patologie MeSH
- neutrofily patologie MeSH
- pankreatická elastasa metabolismus MeSH
- proteiny eozinofilních granul MeSH
- ribonukleasy metabolismus MeSH
- T-lymfocyty metabolismus MeSH
- upregulace * MeSH
- zánět MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD3 MeSH
- antigeny diferenciační myelomonocytární MeSH
- CCL11 protein, human MeSH Prohlížeč
- CD antigeny MeSH
- CD68 antigen, human MeSH Prohlížeč
- chemokin CCL11 MeSH
- chemokiny CC MeSH
- cytokiny MeSH
- interleukin-9 MeSH
- krevní proteiny MeSH
- pankreatická elastasa MeSH
- proteiny eozinofilních granul MeSH
- ribonukleasy MeSH
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.
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