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The aim of this study is to investigate the mechanisms whereby leukocytes are recruited to the lung in chronic obstructive pulmonary disease (COPD) and cause tissue destruction. The hypothesis is that in COPD more leukocytes enter the lung and it is these cells that are responsible for the degradation of lung tissue. We, the researchers at Imperial College London, will isolate leukocytes from the blood of patients with COPD, healthy smokers and normal subjects and measure the movement of the leukocytes to chemoattractants. We will examine further, which cell surface receptors are responsible for this trafficking of cells. Furthermore, the differentiation of these cells in vitro will be compared with cells from healthy smokers and normal subjects. Specifically, the expression of enzymes that are responsible for tissue destruction and the cell surface receptors on these cells will be investigated. The objective is to identify the mechanisms whereby leukocytes from COPD patients behave differently to cells from healthy smokers and normal subjects with a view to identify novel targets for drug therapy.
Chemotaxis experiments will be performed in order to ascertain the migratory characteristics of leukocytes towards specific chemoattractants. Comparisons of cells from different subjects will be compared. In addition, the effects of various pharmaceutical interventions on this mechanism will also be addressed and compared within subject groups. In some experiments, cells will be differentiated in vitro and their cellular expression and regulation of inflammatory mediators and chemoattractants examined. Again comparisons will be made between subject groups and the efficacy of various pharmacological agents on these cells
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| COPD | Patients with COPD - no intervention | ||
| Smokers without COPD | Smokers without COPD - no intervention | ||
| Non-smokers | Non-smokers with no history of respiratory disease - no intervention |
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| Measure | Description | Time Frame |
|---|---|---|
| Effective Concentration (EC 50) of GRO Alpha | Migration response of PBMC to Chemokine EC 50 represents the concentration of a drug that is required for 50% inhibition in vitro | 2 hours |
| Effective Concentration of IL-8 | Migration response of PBMC to Chemokine EC 50 represents the concentration of a drug that is required for 50% inhibition in vitro | 2 hours |
| Effective Concentration of MCP-1 | Migration response of PBMC to Chemokine | 2 hours |
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Inclusion Criteria:
Healthy Non-Smoking Subjects. All normal volunteers will meet the following criteria:
COPD Subjects. COPD is diagnosed according to American Thoracic Society, European Respiratory Society and British Thoracic Society guidelines. All COPD volunteers will meet the following criteria:
Healthy Smokers. All healthy smoking volunteers in trials will meet the following criteria:
Exclusion Criteria:
Subjects will not be included in this study if they meet any of the following exclusion criteria:
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Patients who had taken inhaled or oral steroids or who had suffered an exacerbation of their airway disease in the previous 6 weeks were excluded.
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| Name | Affiliation | Role |
|---|---|---|
| Louise E Donnelly, PhD | Imperial College London | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Royal Brompton Hospital/NHLI Imperial College London | London | SW3 6LY | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 15155777 | Result | Traves SL, Smith SJ, Barnes PJ, Donnelly LE. Specific CXC but not CC chemokines cause elevated monocyte migration in COPD: a role for CXCR2. J Leukoc Biol. 2004 Aug;76(2):441-50. doi: 10.1189/jlb.1003495. Epub 2004 May 20. |
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| ID | Title | Description |
|---|---|---|
| FG000 | COPD | Patients with COPD - no intervention |
| FG001 | Smokers Without COPD | Smokers without COPD - no intervention |
| FG002 | Non-smokers | Non-smokers with no history of respiratory disease - no intervention |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | COPD | Patients with COPD - no intervention |
| BG001 | Smokers Without COPD | Smokers without COPD - no intervention |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Effective Concentration (EC 50) of GRO Alpha | Migration response of PBMC to Chemokine EC 50 represents the concentration of a drug that is required for 50% inhibition in vitro | Posted | Mean | Standard Error | ng/ml | 2 hours |
|
2 hours
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | COPD | Patients with COPD - no intervention | 0 |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Professor Louise Donnelly | Imperial College London | +442075947895 | l.donnelly@imperial.ac.uk |
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| ID | Term |
|---|---|
| D029424 | Pulmonary Disease, Chronic Obstructive |
| D004646 | Emphysema |
| D029481 | Bronchitis, Chronic |
| ID | Term |
|---|---|
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D002908 | Chronic Disease |
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Blood
| BG002 |
| Non-smokers |
Non-smokers with no history of respiratory disease - no intervention |
| BG003 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race and Ethnicity Not Collected | Race and Ethnicity were not collected from any participant. | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Smoking History | Mean | Standard Deviation | pack/years |
|
| FEV1 (% predicted) | Mean | Standard Deviation | % predicted |
|
|
|
|
| Primary | Effective Concentration of IL-8 | Migration response of PBMC to Chemokine EC 50 represents the concentration of a drug that is required for 50% inhibition in vitro | Posted | Mean | Standard Error | ng/ml | 2 hours |
|
|
|
|
| Primary | Effective Concentration of MCP-1 | Migration response of PBMC to Chemokine | Posted | Mean | Standard Error | ng/ml | 2 hours |
|
|
|
|
| 37 |
| 0 |
| 37 |
| 0 |
| 37 |
| EG001 | Smokers Without COPD | Smokers without COPD - no intervention | 0 | 33 | 0 | 33 | 0 | 33 |
| EG002 | Non-smokers | Non-smokers with no history of respiratory disease - no intervention | 0 | 30 | 0 | 30 | 0 | 30 |
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| D020969 |
| Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001991 | Bronchitis |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
| D001982 | Bronchial Diseases |
| Male |
|