Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
50 participants
OBSERVATIONAL
2007-01-31
2007-11-30
Brief Summary
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We hypothesise that a dysfunction of Tregs underlies the development of the inflammatory response in COPD. This could be either due to a decreased presence of Tregs in COPD, or to an altered function of Tregs possibly caused by a decreased HO-1 expression and/or an altered TGFβ regulation.
Detailed Description
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The important role of neutrophils, macrophages and cytotoxic T cells is well established in this respect, yet the role of CD4 T cells and B cells has only recently (re)attracted attention. We detected the presence of lymphoid follicles in lung tissue of COPD patients, consisting of B cells surrounded by T cells. Recently, we have found the presence of Foxp3 positive T cells as a component of these lymphoid follicles in COPD. Since Foxp3 is a distinctive marker of regulatory T cells (Tregs), this finding suggests that Tregs are involved in the inflammatory response in COPD.
Tregs are important in controlling immunological tolerance and preventing auto-immune responses by inhibiting T-cell responses. Dysfunction of Tregs can lead to auto-immune diseases, allergy and chronic inflammatory diseases. However, nothing is known so far about their contribution to the chronic inflammatory response in COPD. Recent studies show that, next to direct inhibition by cell-cell contact, the inhibitory effects of Tregs are mediated by heme oxygenase-1 (HO-1) expression and membrane bound TGFβ.
We hypothesise that a dysfunction of regulatory T cells underlies the development of the inflammatory response in COPD. This could be due to a decreased presence of Tregs in COPD, or to an altered function of Tregs. The latter may be due to a decreased HO-1 expression, as we have shown in macrophages of COPD patients compared to those in healthy controls, and/or an altered TGFβ regulation, a cytokine that plays a prime role in COPD.
Conditions
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Keywords
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Study Design
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PROSPECTIVE
Interventions
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Withdrawal of medication
Eligibility Criteria
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Inclusion Criteria
* Clinical diagnosed COPD
* No allergies
* Post-bronchodilator FEV1 \< 80% predicted, and post-bronchodilator FEV1/FVC \< 70%
* No use of (inhaled) corticosteroids in the 6 weeks preceding the study
* Age \> 40
* Smokers and ex- smokers \> 10 pack years
* Ex-smokers have to have quitted smoking for at least one year
* No other major current health problems
* Informed consent Healthy controls
* No signs of pulmonary disease
* No allergies or hyperreactivity
* No other major current health problems
* FEV1 \> 90 % predicted, FEV1/FVC \> 70%
* Age \> 40
* Never smokers, i.e. no cigarettes last year, and maximal 5 pack years
* Smokers and ex- smokers \> 10 pack years
* Ex-smokers have to have quitted smoking for at least one year
* Informed consent
Exclusion Criteria
* Addiction to alcohol or drugs
* COPD exacerbation in the 6 weeks preceding the study
40 Years
MALE
Yes
Sponsors
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Groningen Research Institute for Asthma and COPD
OTHER
Principal Investigators
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Huib AM Kerstjens, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
UMCG, department of pulmonary diseases
Locations
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University Medical Center Groningen
Groningen, , Netherlands
Countries
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Other Identifiers
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METc2006-135
Identifier Type: -
Identifier Source: org_study_id