Nasal Epithelial Cells/Blood Lymphocyte Markers for Cystic Fibrosis (CF)/CF Pulmonary Exacerbations
Status: | Completed |
---|---|
Conditions: | Pulmonary |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 15 - Any |
Updated: | 2/17/2019 |
Start Date: | September 2006 |
End Date: | September 2011 |
Use of Nasal Epithelial Cells and Blood Lymphocytes to Identify Markers for Cystic Fibrosis and Cystic Fibrosis Pulmonary Exacerbations
Study Hypothesis: We hypothesize that cellular markers from nasal epithelial cells and blood
lymphocytes can serve as potential biomarkers reflect the underlying inflammatory state of
the lung and will be helpful in determining the presence of a CF pulmonary exacerbation and
its overall severity.
lymphocytes can serve as potential biomarkers reflect the underlying inflammatory state of
the lung and will be helpful in determining the presence of a CF pulmonary exacerbation and
its overall severity.
Cystic fibrosis (CF) is the most common lethal genetic disease in the US afflicting
approximately 30,000 people. Chronic disease of the respiratory tract, which is responsible
for early death, affects both the upper and lower airways.
We propose to utilize cells (blood lymphocytes and nasal epithelial cells) that are readily
accessible and are known to express the cystic fibrosis transmembrane conductance regulator
(CFTR) and therefore candidates to express markers of the downstream consequences of CFTR
deficiency.
A marker that indicates the inflammatory state of the lung would be useful to identify
infective/inflammatory exacerbations as opposed to worsening due to pulmonary vascular
disease or simply upper airway infection. This marker might help to guide therapy for
intensity and duration. Evidence in mice suggest that lymphocytes may be a driving force for
inflammation in the CF lung, particularly during exacerbations, and also that human CF
lymphocytes have dysfunctional production of cytokines.
Specific Aims:
To identify markers in nasal epithelial cells or blood lymphocytes that distinguish CF
patients from those with functional CFTR (healthy volunteers and patients with asthma). If
successful this could become a marker for CFTR correction by drugs or other systemic
therapies.
To identify markers in blood lymphocytes that will identify inflammatory status (ie,
distinguish an active exacerbation from return to clinical stability) in CF patients. This
could become a marker for infectious exacerbations of CF airway disease.
approximately 30,000 people. Chronic disease of the respiratory tract, which is responsible
for early death, affects both the upper and lower airways.
We propose to utilize cells (blood lymphocytes and nasal epithelial cells) that are readily
accessible and are known to express the cystic fibrosis transmembrane conductance regulator
(CFTR) and therefore candidates to express markers of the downstream consequences of CFTR
deficiency.
A marker that indicates the inflammatory state of the lung would be useful to identify
infective/inflammatory exacerbations as opposed to worsening due to pulmonary vascular
disease or simply upper airway infection. This marker might help to guide therapy for
intensity and duration. Evidence in mice suggest that lymphocytes may be a driving force for
inflammation in the CF lung, particularly during exacerbations, and also that human CF
lymphocytes have dysfunctional production of cytokines.
Specific Aims:
To identify markers in nasal epithelial cells or blood lymphocytes that distinguish CF
patients from those with functional CFTR (healthy volunteers and patients with asthma). If
successful this could become a marker for CFTR correction by drugs or other systemic
therapies.
To identify markers in blood lymphocytes that will identify inflammatory status (ie,
distinguish an active exacerbation from return to clinical stability) in CF patients. This
could become a marker for infectious exacerbations of CF airway disease.
Stable CF Patients:
Inclusion Criteria:
- Male or female >= 15 years of age
- Confirmed diagnosis of CF
- Clinically stable with no evidence of acute upper respiratory tract infection or
current pulmonary exacerbation within the previous month
- Ability to understand and sign a written informed consent and comply with the
requirements of the study
Exclusion Criteria:
- Chronic use of a medication with anti-neutrophil or anti-inflammatory effect
(ibuprofen, systemic or inhaled corticosteroids, or other immunosuppressive agents,
etc
- Oxygen saturation <92% on room air
- Presence of a condition or abnormality that in the opinion of the Investigator would
compromise the safety of the subject or the quality of the data
CF patients with pulmonary exacerbations:
Male of female >= 15 years of age Confirmed diagnosis of CF
Patient meets a modified definition for a pulmonary exacerbation based upon Fuchs criteria
which is treated with intravenous antibiotics for any 4 of the following 12 signs or
symptoms:
- Increased sputum production
- New or increased coughing up of blood
- Increased cough
- Increased dyspnea with exertion
- Malaise, fatigue or lethargy
- Anorexia or weight loss
- Fever
- Sinus pain or tenderness
- Changes in sinus discharge
- New findings on chest examination
- Decline in forced expiratory volume in 1 second (FEV1) > 10% since previous visit
- Radiographic changes indicative of pulmonary infection
- Ability to understand and sign a written informed consent and comply with the
requirements of the study
Exclusion criteria for CF patients with pulmonary exacerbation:
- Concurrent use a medication with anti-neutrophil or anti-inflammatory effect within
the previous 4 weeks
- Presence of a condition or abnormality that in the opinion of the investigator would
compromise the safety of the subject or the quality of the data.
Inclusion Criteria - Asthma patients
- Male or female >= 15 years of age
- Physician diagnosed asthma
- Clinically stable with no evidence of acute upper or lower respiratory tract infection
or current pulmonary exacerbation within the previous month
Exclusion Criteria - Asthma patients
- Chronic use of a medication with anti-neutrophil or anti-inflammatory effect within
the previous 4 weeks
- Treated for an asthma exacerbation with the previous 4 weeks
- Treated with oral corticosteroids within the previous 4 weeks
- Oxygen saturation <92% on room air
- Presence of a condition or abnormality that in the opinion of the investigator would
compromise the safety of the subject or the quality of the data.
Inclusion Criteria for Healthy Volunteers
- Male or female >= 18 years of age
- Free of any chronic medical condition
- Clinically stable with no evidence of acute upper or lower respiratory tract infection
within the previous month
- Ability to understand and sign a written informed consent and comply with the
requirements of the study
Exclusion Criteria for Healthy Volunteers
- Use of a medication with anti-neutrophil or anti-inflammatory effect within the
previous 4 months
- Presence of any chronic medical condition
- Oxygen saturation <92% on room air
- Presence of a condition or abnormality that in the opinion of the Investigator would
compromise the safety of the subject or the quality of the data
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